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ORIGINAL RESEARCH article

Front. Pharmacol., 14 May 2021
Sec. Ethnopharmacology
This article is part of the Research Topic Emerging and Old Viral Diseases: Antiviral Drug Discovery from Medicinal Plants View all 8 articles

Broad Anti-Viral Capacities of Lian-Hua-Qing-Wen Capsule and Jin-Hua-Qing-Gan Granule and Rational use Against COVID-19 Based on Literature Mining

  • 1Institute of Basic Theory for Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China
  • 2State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao, China
  • 3The Third School of Clinical Medicine, Nanjing University of Chinese Medicine, Nanjing, China
  • 4Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China
  • 5Department of Nephropathy, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China

The novel coronavirus disease 2019 (COVID-19) has become a matter of international concern as the disease is spreading exponentially. Statistics showed that infected patients in China who received combined treatment of Traditional Chinese Medicine and modern medicine exhibited lower fatality rate and relatively better clinical outcomes. Both Lian-Hua-Qing-Wen Capsule (LHQWC) and Jin-Hua-Qing-Gan Granule (JHQGG) have been recommended by China Food and Drug Administration for the treatment of COVID-19 and have played a vital role in the prevention of a variety of viral infections. Here, we desired to analyze the broad-spectrum anti-viral capacities of LHQWC and JHQGG, and to compare their pharmacological functions for rational clinical applications. Based on literature mining, we found that both LHQWC and JHQGG were endowed with multiple antiviral activities by both targeting viral life cycle and regulating host immune responses and inflammation. In addition, from literature analyzed, JHQGG is more potent in modulating viral life cycle, whereas LHQWC exhibits better efficacies in regulating host anti-viral responses. When translating into clinical applications, oral administration of LHQWC could be more beneficial for patients with insufficient immune functions or for patients with alleviated symptoms after treatment with JHQGG.

Introduction

Lian-Hua-Qing-Wen Capsule and Jin-Hua-Qing-Gan Granule are Both Recommended as Effective “Chinese Solution” Against COVID-19

The novel coronavirus disease 2019 (COVID-19) pandemics has reached almost every country in the world. Compared with the outbreak of Severe Acute Respiratory Syndrome (SARS) in 2003 and the pandemic of Middle East Respiratory Syndrome (MERS) in 2012, COVID-19 caused by the novel coronavirus SARS-CoV-2 infection has relatively low fatality rate, whereas much more rapid and higher human-to-human transmissibility (Meo et al., 2020). Typically, the existence of a large number of asymptomatic carriers of SARS-CoV-2 additionally exerts potential burden to the control and prevention of COVID-19.

SARS-CoV-2 can be easily transmitted through respiratory droplets or by aerosol, and infected people have a wide range of reported symptoms, from mild symptoms to severe illness. The most common manifestations of COVID-19 are fever or chill, dry cough and fatigue, which could be accompanied with a temporary loss of smell or taste, muscle or body aches. In critical cases, acute myocardial injury, liver or kidney dysfunction and blood-clotting complications may occur Huang et al. (2020), Khider et al. (2020), consequently leading to septic shock and acute respiratory distress syndrome (ARDS) or death. The “Clinical Treatment for COVID-19” issued by the World Health Organization recommends that symptomatic treatments that relieve fever and pain, together with adequate nutritional supports are basically required for mild cases of COVID-19. For severe SARS-CoV-2 infections, oxygen therapy and fluid supply need to be reinforced. In spite of supportive measures above, potential anti-viral drugs which were used for diseases due to viral infections other than SARS-CoV-2 have been repurposed for COVID-19, such as remdesivir, ribavirin and hydroxychloroquine are however not addressed because of reported side-effects or lack of supporting evidence from large-scale randomized controlled trials (Izcovich et al., 2020; Trivedi et al., 2020; Qaseem et al., 2021). Likewise, vaccine development involves a difficult, complex and costly process, and the success of which is at a high risk of failure protecting against mutant viral variants (Biswas and Majumder, 2020; Penarrubia et al., 2020). Despite the development of vaccines, scientists are still tirelessly designing new drugs and repurposing existing drugs against SARS-CoV-2. Though tremendous strides have been made in the fight against coronaviruses, a lack of safe and effective anti-SARS-CoV-2 drugs is still a key factor restricting the prevention and control of COVID-19 pandemics.

The practice of Traditional Chinese Medicine (TCM) has accumulated a wealth of clinical experience in the treatment of infectious diseases since Qin-Han (about 221 BC to 220 AD) and developed into a theory in Ming-Qing period (about 1,368–1777 AD). Infectious diseases in TCM have been described as “infections caused by toxic qi”, “warm pathogen first invades lung via nose and mouth”, and “disease spreads due to close contact”. These descriptions fit well with the epidemiological characteristics of modern acute infectious diseases. According to TCM theory, COVID-19 is the result of invasion by dampness-toxin pathogens, therefore COVID-19 is pathogenically characterized by dampness-toxin and host healthy-qi deficiency. Most patients first present mild sign of dampness, like fatigue, poor appetite and greasy thick tongue coating (Zheng, 2020). As disease progresses, dampness-toxin invades interiority and diffuses into triple energizer, leading to vital qi impairment and accumulation of toxin-qi in viscera. Excessive accumulation of dampness-toxin may easily lead to vital qi exhaustion and consequently loss of life. Hence, TCM formulae functioning to remove dampness-toxin are effective in preventing COVID-19 progress. Being the first country that was attacked by COVID-19, approximately 91.5% confirmed patients in China were treated with TCM formulae and the total effective rate has reached to 90%. In Wuhan Jiang-Xia Square Cabin Hospital, none of the 564 COVID-19 patients who received combined treatment of TCM and modern medicine developed into severe conditions, and TCM addition significantly reduced the course of hospitalization (Ren et al., 2020).

Both LHQWC and JHQGG belong to “Three Drugs, Three Prescriptions”, official prescriptions of TCM used in the fight against COVID-19 in China. LHQWC, composed of Forsythia suspensa (Thunb.) Vahl, Lonicera japonica Thunb., honey-fried Ephedra sinica Stapf, fried Prunus sibirica L., Gypsum Fibrosum, Isatis tinctoria L., Dryopteris crassirhizoma Nakai, Houttuynia cordata Thunb., Pogostemon cablin (Blanco) Benth., Rheum palmatum L., Rhodiola crenulata (Hook.f. and Thomson) H. Ohba, Mentha canadensis L. and Glycyrrhiza glabra L., is innovative Chinese Patent Medicine (CPM) approved during the SARS epidemics in 2003. JHQGG, the other CPM constituting Forsythia suspensa (Thunb.) Vahl, Lonicera japonica Thunb., Ephedra sinica Stapf, Prunus sibirica L., l-Menthol, Glycyrrhiza glabra L., Scutellaria baicalensis Georgi, Fritillaria thunbergii Miq., Anemarrhena asphodeloides Bunge, Arctium lappa L. and Artemisia annua L., has been approved to treat H1N1 influenza virus infection since 2009. Both LHQWC and JHQGG are developed based on Ma-Xing-Shi-Gan Decoction and Yin-Qiao Powder, classic TCM decoctions used for respiratory infections recorded in Treatize on Exogenous Febrile Disease (about 210 AD) and Systematic Differentiation of Warm Diseases (1798 AD), respectively. In clinical practices resolving respiratory infections, LHQWC is mainly used to clear away plague, remove toxins, ventilate lungs and discharge heat, whereas JHQGG is applied to dispel wind, clear heat and resolve toxin. In the combat against COVID-19, National Health Commission of China approved both LHQWC and JHQGG as clinical therapies in China, and observational studies showed that both can effectively relieve fever, fatigue, cough and phlegm in the early stage of COVID-19, contributing to reductions in risks of rapid clinical deterioration. Supportively, in vitro studies have revealed that both formulae have anti-inflammatory effects, providing fundamental evidence for clinical application of both formulae in the fight against COVID-19 (Cheng, 2020; Duan, 2020; Hu et al., 2020; Runfeng et al., 2020; Zhang et al., 2020).

Holism Theory of TCM and Anti-viral Actions of Lian-Hua-Qing-Wen Capsule and Jin-Hua-Qing-Gan Granule, a Reflection of Host-Directed Therapy in Modern Medicine

Holism is the fundamental concept in TCM, which emphasizes the connections of the whole body and intends to treat the whole person rather than focusing on individual symptoms. Directed by holistic view, TCM practitioners adopt syndrome differentiation (Bian Zheng), a comprehensive analysis of a variety of clinical information, and herbal formulae to resolve single or complex uncomfortability of patients. This holism theory of TCM dovetails with the principle of host-directed therapy (HDT). HDT is a novel concept in the treatment for infectious diseases and was first used in tuberculosis in 2015 (Zumla et al., 2015). After then, HDT was gradually fulfilled as anti-viral strategies. Compared to conventional anti-viral therapies, which focus on inhibiting virus activity, HDT aims to maintain homeostasis of host by stimulating anti-viral responses and suppressing immune injuries. It has been shown that compared to single anti-pathogen treatment, HDT is able to reduce the risks of drug resistance induced by bacteria and viruses, endowing HDT a therapeutic potential of being broad-spectrum anti-viral tactics (Kaufmann et al., 2018). Clinical investigations proposed that viral infection-triggered cytokine storm was a vital factor mediating the rapid progress of COVID-19 (Wang T. et al., 2020). High levels of IL (Interleukin) -6 and IL-10, while low levels of CD4+ T and CD8+ T cells can be observed in COVID-19 patients (Guan et al., 2020; Wan et al., 2020). Moreover, plasma IL-2, IL-7, IL-10, GCSF (granulocyte colony-stimulating factor), IP-10 (interferon gamma-induced protein-10), MCP-1 (monocyte chemoattractant protein-1), MIP-1α (macrophage inflammatory protein-1 alpha) and TNF-α (tumor necrosis factor-alpha) are consistently higher in intensive care unit (ICU) patients compared to mild cases (Huang et al., 2020), suggesting that virus-induced exaggerated immune responses and the resulting immune injuries are involved in the progression of COVID-19. Accordingly, HDT-oriented treatments that inhibit IL-6 signaling by down-regulating IL-6 receptors have been suggested as a potential solution for COVID-19 patients (Zumla et al., 2020). Consistent with HDT, in the combat against COVID-19, TCM addresses that sufficient healthy-qi within the body is key to prevent pathogen invasion, so-called “strengthening host resistance to eliminate pathogenic factors”. Accordingly, inspiring vital qi is at the root of preventing infectious diseases in TCM. The functions of “healthy-qi” resemble “immunity” of host, and “pathogenic factors” stand for all substances that affect host homeostasis, such as viruses and bacteria. As emphasized in HDT that considering individuals as a whole rather than separating parts, “strengthening host resistance to eliminate pathogenic factors” in TCM addresses an overall reaction of host in response to invasive viruses, whereas the destiny of pathogen itself is not primarily important. Moreover, same as the HDT concept implicates, the ultimate goal of TCM treatment is to maintain host homeostasis via balancing interactions between host and pathogens, or by establishing equilibrium between stimulating anti-viral reactions and suppressing overactivated immune responses that subsequently cause tissue injuries.

Following the HDT principle and holism theory of TCM, this study primarily desired to gain more insight into the broad anti-viral features of LHQWC and JHQGG, both of which have been applied to treat a variety of viral infections. However, considering that the main herbal composition of LHQWC and JHQGG largely overlap, it therefore appears confusing in the selection of appropriate formula for individual clinical cases. In this scenario, it is of prime importance to also distinguish the similarities and differences between the two formulae in terms of pharmacological anti-viral functions. To implement these goals, we manually grouped the individual active components from either LHQWC or JHQGG or both into two categories, namely constituents that interfere with viral life cycle and components that regulate host immune responses and inflammation. Through comprehensive literature review, data mining and pharmacological target enrichment analysis, we investigated the strength of LHQWC and JHQGG in the above-mentioned virus or host arm to compare their anti-viral functionalities. The holism-directed analysis of LHQWC and JHQGG will provide more insightful information and comprehensive understanding for rational use of these two CPMs in the combat against COVID-19, as well as the emerging or re-emerging pandemics of infectious diseases.

Materials and Methods

Literature Collection and Inclusion

In order to collect sufficient data on anti-viral effects of LHQWC and JHQGG, we employed Pubmed (https://pubmed.ncbi.nlm.nih.gov), Ovid (https://ovidsp.ovid.com/), CNKI (https://www.cnki.net), WANFANG (http://www.wanfangdata.com.cn/index.html) and WEIPU (http://www.cqvip.com/) database by searching either the full name of formulae, such as “Lianhua Qingwen Capsules”, “Jinhua Qinggan Granules”, or names of individual medicinal herbs, or active ingredients, together with “virus” as keywords. In addition, bioactive components that were proposed to be antivirals were included via network pharmacology-based prediction and analysis. A total of 1,110 articles were collected for next filtration. For the analysis of broad anti-viral activities, we then excluded studies reporting negative outcomes, clinical trials generally indicating viral infections without clarifying taxonomy of viruses, investigations using inactivated or attenuated viruses as vaccines, and articles with no access to full context due to age. A total of 812 articles were analyzed at this stage. For detailed comparisons of active anti-viral components and pharmacological functions of formulae, studies without indicating names of active components were further excluded. Notably, no information regarding Gypsum Fibrosum and fried Prunus sibirica L. in relevant to virus, and we did not find data by searching bioactive components directly isolated from JHQGG, hence we only took ingredients determined by predictive parsing of network pharmacology. Finally, 117 articles were included for comparison of pharmacological functions.

Constructing “Formula–Herb–Virus–Baltimore Classification of Viruses” Network

In order to describe broad-spectrum anti-viral activities of LHQWC and JHQGG, we grouped antiviral data collected as mentioned, and built a network in forms of “Formula-herb-virus-Baltimore classification of viruses”. To further interpret the common and distinctive anti-viral activities of LHQWC and JHQGG in terms of holism theory of TCM, we classified the anti-viral actions reported for LHQWC and JHQGG into being either associated with viral life cycle or responsible to host immune responses and inflammation. To gain more insightful understanding, we further categorized active components that disrupt virus life cycle into three levels, including direct virucidal activity, inhibition of viral entry, and suppression of viral replication and egress. Generally, inhibitors of virus entry act through deforming viral particles or blocking the attachment or binding of virions to host cells. The control of virus replication is mainly mediated by inhibiting replicator machineries encoded by viral systems, and prevention of virus egress is a process involves an interference with assembly and release of progeny viruses, which may initiate a secondary round infection. For the actions of regulating host immune responses and inflammation, it represents any virucidal effects due to an indirect response by modulating host immune system, such as increasing interferons (IFNs) expression, or decreasing self-targeted inflammatory injuries, or promoting repair process post virus infection without involving viral molecule-associated biological events. Based on literature mining and analysis, we next counted the frequencies of active components of LHQWC and JHQGG that have been sorted into each of the two categories, and accordingly a radar chart was drawn to visualize and compare the power of LHQWC and JHQGG against viral infection in terms of modulating viral life cycle and regulating host immune responses and inflammation.

Results

The broad-Spectrum Anti-Viral Activities of Lian-Hua-Qing-Wen Capsule and Jin-Hua-Qing-Gan Granule

Multi-ingredients, multi-targets and multi-pathways are primary features of TCM formulae, suggesting that active ingredients of one medicinal herb may exert anti-viral functions via diverse pharmacological mechanisms. As shown in Figure 1, active components in both LHQWC and JHQGG have been shown to target 87 different types of viruses, covering all the seven classes according to the Baltimore classification. This wide range of anti-viral activities of LHQWC and JHQGG addresses that TCM formulae used in COVID-19 pandemics could be potentially applied for other virological infections, such as influenza A virus, Zika virus and herpesvirus.

FIGURE 1
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FIGURE 1. The broad-spectrum anti-viral activities of LHQWC and JHQGG. The “Formula–herb–virus–Baltimore classification of viruses” profile demonstrating a broad-spectrum anti-viral activity of LHQWC and JHQGG. In the center, medicinal herbals exclusively existing in LHQWC, including HQ (Scutellaria baicalensis Georgi, Huang Qin); ZBM (Fritillaria thunbergii Miq., Zhe Bei Mu); ZM (Anemarrhena asphodeloides Bunge, Zhi Mu); QH (Artemisia annua L., Qing Hao) and NBZ (Arctium lappa L., Niu Bang Zi) are shown in orange; medicinal herbals found only in JHQGG, including MMGZ (Dryopteris crassirhizoma Nakai, Mian Ma Guan Zhong); HJT (Rhodiola crenulata (Hook.f. and Thomson) H. Ohba, Hong Jing Tian); DH (Rheum palmatum L., Da Huang); GHX (Pogostemon cablin (Blanco) Benth., Guang Huo Xiang); BLG (Isatis tinctoria L., Ban Lan Gen) and YXC (Houttuynia cordata Thunb., Yu Xing Cao); are presented in green; common herbs used in both LHQWC and JHQGG, including LQ (Forsythia suspensa (Thunb.) Vahl, Lian Qiao); GC (Glycyrrhiza glabra L., Gan Cao); BH (Mentha canadensis L., Bo He); MH (Ephedra sinica Stapf, Ma Huang) and JYH (Lonicera japonica Thunb., Jin Yin Hua) are colored in blue. The circle marked in orange represents 87 types of viruses, and the cycle in the periphery indicates Baltimore classification of these viruses. Colored squares sitting between the circle of individual herbs and 87 viruses indicate that components existing only in LHQWC (orange) or only in JHQGG (green) or in both formulae (blue) have been reported effective to treat diseases caused the corresponding viruses. AdV, Adenoviruses; ASLV, Avian sarcoma leukosis virus; BoHV, Bovine alphaherpesvirus; BPV, Bovine papillomavirus; BVDV, Bovine viral diarrhea virus; CDV, Canine distemper virus; CHIKV, Chikungunya virus; CLSV, Cucumber leaf spot virus; Cox A, Coxsackie A virus; Cox B, Coxsackie B virus; CPV, Canine parvovirus; CSFV, Classical swine fever virus; DENV, Dengue virus; DHAV, Duck hepatitis A virus; DHBV, Duck hepatitis B virus; EBOV, Ebola virus; EBV, Epstein–Barr virus; ECHO, Echovirus; EHV, Equine herpes virus; EMCV, Encephalomyocarditis virus; EV71, Enterovirus A 71; GCRV, Grass carp reovirus; GPCMV, Guinea pig cytomegalovirus; GPV, Goose parvovirus; HAV, Hepatitis A virus; HBV, Hepatitis B virus; HCMV, Human cytomegalovirus; HCV, Hepatitis C virus; HDV, Hepatitis D virus; HEV, Hepatitis E virus; HHV, Human herpesvirus; HIV, Human immunodeficiency virus; HMPV, Human metapneumovirus; HPIV, Human parainfluenza virus; HPV, Human papillomavirus; HSV, Herpes simplex virus; HTLV, Human T lymphotropic virus; HV, Hantavirus; IBDV, Infectious bursal disease virus; IBV, Infectious bronchitis virus; JEV, Japanese encephalitis virus; KSHV, Kaposi's sarcoma herpesvirus; MCMV, Murine cytomegalovirus; MDV, Marek's disease virus; MERS-CoV, Middle East respiratory syndrome coronavirus; MHV, Mouse Hepatitis virus; MLV, Murine leukemia virus; MMLV, Moloney Murine Leukemia virus; MuV, Mumps virus; NDV, Newcastle disease virus; NV, Norovirus; PCV, Porcine circovirus; PDCoV, Porcine deltacoronavirus; PEDV, Porcine epidemic diarrhea virus; PepMV, Potato–Pepino mosaic virus; PPV, Porcine parvovirus; PPMV, pigeon paramyxovirus; PPV, Pigeonpox virus; PRRSV, Porcine reproductive and respiratory syndrome virus; PRSV, Papaya ringspot virus; PrV, Pseudorabies virus; Rous SV, Rous sarcoma virus; RRV, Ross River virus; RSV, Respiratory syncytial virus; RuV, Rubella virus; RV, Rotavirus; RV-A, SA-11 Simian rotavirus; SARS-CoV, Severe acute respiratory syndrome coronavirus; SARS-CoV-2, Severe acute respiratory syndrome coronavirus 2; SeV, Sendai virus; SFV, Semliki Forest virus; SIV, Simian immunodeficiency virus; SV40, Simian virus 40; TBEV, Tick-borne encephalitis virus; TGEV, Transmissible Gastroenteritis virus; TMV, Tobacco mosaic virus; VSV, Vesicular stomatitis virus; VZV, Varicella zoster virus; WMV, Watermelon mosaic virus; WNV, West Nile virus; YFV, Yellow fever virus; ZIKV, Zika virus. RNA, Ribonucleic Acid; -ssRNA, Negative-sense single-strand RNA; +ssRNA, Positive-sense single-stranded RNA; dsRNA, Double-stranded RNA; ssRNA-RT, Single-stranded RNA virus-reverse transcriptase; DNA, Deoxyribonucleic Acid; ssDNA, Single-stranded DNA; dsDNA, Double-stranded DNA; dsDNA-RT, Double-stranded DNA virus-reverse transcriptase.

Similarities and Differences of Lian-Hua-Qing-Wen Capsule and Jin-Hua-Qing-Gan Granule as Antivirals

Both LHQWC and JHQGG possess broad-spectrum anti-viral potentials through interfering with viral life cycle and modulating host immune responses, which are associated with a diversity of proposed pharmacological actions as detailed in Tables 1, 2, 3; Figure 2. When comparing LHQWC and JHQGG, no difference was found in the types of their targeted viruses (Table 1; Figure 1). In terms of active components that disrupt viral life cycle (Table 1; Figure 2), only few literatures reported a direct virucidal activity from components of LHQWC and JHQGG (Table 1-1.1; Figure 2), about 24% studies showed suppression of viral entry (Table 1-1.2; Figure 2), while 70% studies focused on inhibitory effects toward viral replication and release (Table 1-1.3; Figure 2) Among all data analyzed, constituents from Scutellaria baicalensis Georgi (Huang Qin) of JHQGG have been mostly reported to interfere with viral life cycle in all three phases analyzed. Besides, components from Isatis tinctoria L (Ban Lan Gen) and Rheum palmatum L (Da Huang) of LHQWC are shown highly effective in blocking viral entry, replication and release. JHQGG weights slightly higher than LHQWC in terms of viral replication and release, whereas little difference was obtained in the early phase of viral life cycle (Table 1; Figure 2). Regarding “host immune responses and inflammation”, it is interesting that constituents from Scutellaria baicalensis Georgi (Huang Qin) of JHQGG again exhibited the greatest potential, followed by components from Isatis tinctoria L (Ban Lan Gen) and Rheum palmatum L (Da Huang) in LHQWC. When comparing LHQWC and JHQGG, LHQWC weights slightly higher than JHQGG (Table 2; Figure 2). In addition, several studies have proposed other anti-viral mechanisms that could not be grouped into the above two categories, such as maintaining host redox homeostasis, or acting on microbiota, or gut-lung axis, or energy sensor AMPK, or autophagy (Table 3; Figure 2). Detailed information regarding the TCM features, pharmacological functions of individual herbs and components was outlined in Table 4.

TABLE 1
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TABLE 1. Active anti-viral components from LHQWC and JHQGG, and their mechanisms of action regulating viral life cycle.

TABLE 2
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TABLE 2. Active anti-viral components from LHQWC and JHQGG regulating host immune responses and inflammation.

TABLE 3
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TABLE 3. Active anti-viral components from LHQWC and JHQGG regulating host redox homeostasis and other molecular actions.

FIGURE 2
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FIGURE 2. Comparison of anti-viral mechanisms between LHQWC and JHQGG. Anti-viral potentials of LHQWC and JHQGG are grouped into five categories, which are defined as (A). Direct virucidal activity, (B). Inhibit viral entry, (C). Inhibit viral replication and egress, (D). Regulate host immune responses and inflammation and (E). Regulate host redox and others”. The percentage in each category indicates the power of both LHQWC and JHQGG in individual anti-viral actions, among which the “A. Direct virucidal activity” and “B. Inhibit viral entry” belong to the early phase of viral infection as marked by black dotted line; the “A. Direct virucidal activity”, “B. Inhibit viral entry” and “C. Inhibit viral replication and egress”together constitute the whole viral life cycle, as surrounded in black. Comparation of LHQWC and JHQGG is demonstrated in the center, with actions from components only in LHQWC shown in blue, only of JHQGG in red, and for both LHQWC and JHQGG are circled within the black dotted area. 0–40 represents counted frequencies of either LHQWC or JHQGG in each of the five categories.

TABLE 4
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TABLE 4. Detailed information of TCM features and pharmacological functions of single medicinal herbs from LHQWC and JHQGG.

In terms of COVID-19, the ACE-2 has been identified as the most important receptor for SARS-CoV-2 viral entry, which constitutes the initial step of infection (Walls et al., 2020). Through informatic analysis, the Rheum palmatum L (Da Huang) in LHQWC was found to be able to suppress viral infection by directly blocking interactions between the spike protein and ACE2. In addition, in the SARS-CoV, MERS-CoV and other coronaviruses, the 3CL (3C-like) protease is one of the crucial enzymes that mediates viral replication and has been recognized as a potential therapeutic target (Pillaiyar et al., 2016; Galasiti Kankanamalage et al., 2018). These predictive evaluations showed that Scutellaria baicalensis Georgi (Huang Qin), Anemarrhena asphodeloides Bunge (Zhi Mu) and Arctium lappa L (Niu Bang Zi) in JHQGG, as well as Rheum palmatum L (Da Huang) and Houttuynia cordata Thunb (Yu Xing Cao) in LHQWC can inhibit viral transcription and replication, especially that the Rheum palmatum L (Da Huang) in LHQWC was shown as a potential inhibitor of 3CL protease, suggesting underlying mechanisms of both LHQWC and JHQGG in the treatment of COVID-19.

Since LHQWC and JHQGG are both commonly used for the treatment of influenza in China, we additionally analyzed their possible roles in the inhibition of influenza viral invasion. Hemagglutinin (HA) on the surface of influenza virus is a tri-polymer, which promotes virus binding and entering into host cells. In contrast to HA, the neuraminidase (NA) of influenza viruses involves detachment and release of mature viruses from host cells (Gamblin and Skehel, 2010; Gaymard et al., 2016). Components of Scutellaria baicalensis Georgi (Huang Qin) of JHQGG have been shown to inhibit the whole life cycle of influenza viruses, such as inhibiting HA and NA, and suppressing replicons. Meanwhile, Isatis tinctoria L (Ban Lan Gen) and Rheum palmatum L (Da Huang) of LHQWC have also been reported to reduce the internalization and replication of influenza viruses. The shared herbs, such as Ephedra sinica Stapf (Ma Huang), Lonicera japonica Thunb (Jin Yin Hua), Forsythia suspensa (Thunb.) Vahl (Lian Qiao) and Glycyrrhiza glabra L (Gan Cao) in both LHQWC and JHQGG were experimentally proved as inhibitors of influenza virus life cycle (Table 1; Table 1).

Discussion

In clinical practices of TCM, medicinal herbs are generally applied in the form of decoctions, which contain mixtures of a variety of herbs with different pharmacological functions. Instead of directly inactivating pathogens, therapeutic effects of TCM decoctions are achieved mainly through balancing host anti-viral responses and pathogenic factors. During COVID-19 epidemics, synergistic therapy of LHQWC with clinically approved reproposing antivirals, such as oseltamivir, umifenovir, ribavirin, lopinavir, peramivir, penciclovir or ganciclovir, has shown its advantages in improving associated symptoms and reducing the course of hospitalization and disease progression in several reported trials (Liu M. et al., 2020; Yu, 2020a; Yu, 2020b; Cheng, 2020; Hu et al., 2020; Li et al., 2020; Lv and Wang, 2020; Xiao et al., 2020; Chen, 2021; Liu et al., 2021). Similarly, combined anti-viral treatment with JHQGG in mild or moderate COVID-19 was beneficial in relieving clinical symptoms and reducing risks of severe COVID-19 (Liu Z. et al., 2020; Duan, 2020; Duan, 2020). These studies provide clinical evidence that combined treatment with either LHQWC or JHQGG is superior to conventional monotherapy of antivirals.

The primary conclusion of our study that both LHQWC and JHQGG are efficient for a large range of viral diseases has supported that TCM formulae can be potentially an alternative therapy for emerging viral diseases, especially when specific drugs and vaccines have not been fully developed and applied. However, when it comes to appropriate or precisive clinical applications of LHQWC and JHQGG, differences of their associated pharmacological actions turn out to be an essential point to be addressed. When comparing the anti-viral targets of LHQWC and JHQGG, both CPMs have been documented effective in interfering with viral components, with Isatis tinctoria L (Ban Lan Gen) and Rheum palmatum L (Da Huang) in LHQWC being the predominate viral inhibitors, followed by Lonicera japonica Thunb (Jin Yin Hua) and Houttuynia cordata Thunb (Yu Xing Cao). While in JHQGG, the Scutellaria baicalensis Georgi (Huang Qin) and subsequently Lonicera japonica Thunb (Jin Yin Hua) are the most important virucidal herbs. Typically, Scutellaria baicalensis Georgi (Huang Qin) of JHQGG have been highly nominated among all analyzed herbs contributing to suppression of the whole viral life cycle. Intriguingly, a direct virucidal activity was observed mostly in components from Scutellaria baicalensis Georgi (Huang Qin) and Anemarrhena asphodeloides Bunge (Zhi Mu) of JHQGG, though shared herbs, Lonicera japonica Thunb (Jin Yin Hua) and Glycyrrhiza glabra L (Gan Cao) were also involved. This set of data indicate that from the angle of viral life cycle, JHQGG may overweight LHQWC due to Scutellaria baicalensis Georgi (Huang Qin), and will be appropriate for patients with high fever, sore throat and cough. On the other hand, owning to existence of Rhodiola crenulata (Hook.f. and Thomson) H. Ohba (Hong Jing Tian), LHQWC may have more essential roles in the balancing of host immunity, suggesting that LHQWC could be more suitable for patients with non-efficient anti-viral immune responses.

There are some possible limitations in this study. Firstly, based on five databases, we finally included relatively more articles associated with LHQWC compared with those of JHQGG; therefore, bias could be unintendedly introduced to conclusions supporting superiority of LHQWC. Secondly, a certain number of included studies focus on Scutellaria baicalensis Georgi (Huang Qin), Isatis tinctoria L (Ban Lan Gen) and Rheum palmatum L (Da Huang); therefore, this may lead to biases that only these herbs are important as antivirals. Thirdly, the quality of articles included in this study is variable, and the judgment for potential pharmacological actions may to some degree rely on the knowledge of authors.

COVID-19 initiates with mild or moderate symptoms in most cases, and the strategy to reduce risks in evolving into severe or critical COVID-19 is highly desired. Through literature mining, we provide general evidence that both LHQWC and JHQGG are effective for mild to moderate COVID-19 patients and potentially being able to prevent the progress of COVID-19 into severe or critical conditions. As discussed above, TCM therapy fits well with the principle of HDT, and anti-viral TCM formulae generally show a broad spectrum of anti-viral properties through balancing between viral activities and host immune reactions. This has gained TCM a key advantage over target-specific anti-viral medications. Since LHQWC and JHQGG are both CPMs with clear safety information, it is imperative that application of LHQWC and JHQGG can be contextualized to worldwide combat against the emerging or re-emerging of human pandemics.

Data Availability Statement

The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding authors.

Author Contributions

NL, RX and JL initiated and supervised this study. NL, RX, MS, BP, and AL performed data analysis and wrote this manuscript. PS assisted in organizing and analyzing data, and ZL contributed to editing.

Funding

This research was funded by a grant from the Key Projects for International Cooperation on Science, Technology and Innovation (2020YFE0205100), and Fundamental Scientific Research of Central Public Welfare Foundation from China Academy of China Medical Sciences (YZ-202012).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

Authors thank Zhenji LI, World Federation of Chinese Medicine Societies for his supports and valuable input.

References

Ahn, H., Lee, S. Y., Kim, J. W., Son, W. S., Shin, C. G., and Lee, B. J. (2001). Binding Aspects of Baicalein to HIV-1 Integrase. Mol. Cells 12 (1), 127–130.

Google Scholar

Bae, G., Yu, J.-R., Lee, J., Chang, J., and Seo, E.-K. (2007). Identification of Nyasol and Structurally Related Compounds as the Active Principles fromAnemarrhena Asphodeloides against Respiratory Syncytial Virus (RSV). Chem. Biodivers. 4 (9), 2231–2235. doi:10.1002/cbdv.200790181

CrossRef Full Text | Google Scholar

Bao, L. D., Ren, X. H., Ma, R. L., Wang, Y., Yuan, H. W., and Lv, H. J. (2015). Efficacy of Artemisia Annua Polysaccharides as an Adjuvant to Hepatitis C Vaccination. Genet. Mol. Res. 14 (2), 4957–4965. doi:10.4238/2015.may.11.29

PubMed Abstract | CrossRef Full Text | Google Scholar

Biswas, N. K., and Majumder, P. P. (2020). Analysis of RNA Sequences of 3636 SARS-CoV-2 Collected from 55 Countries Reveals Selective Sweep of One Virus Type. Indian J. Med. Res. 151, 450-458. doi:10.4103/ijmr.IJMR_1125_20

PubMed Abstract | CrossRef Full Text | Google Scholar

Blach-Olszewska, Z., Jatczak, B., Rak, A., Lorenc, M., Gulanowski, B., Drobna, A., et al. (2008). Production of Cytokines and Stimulation of Resistance to Viral Infection in Human Leukocytes by Scutellaria Baicalensis Flavones. J. Interferon Cytokine Res. 28 (9), 571–581. doi:10.1089/jir.2008.0125

PubMed Abstract | CrossRef Full Text | Google Scholar

Blazquez, A. G., Fernandez-Dolon, M., Sanchez-Vicente, L., Maestre, A. D., Gomez-San Miguel, A. B., Alvarez, M., et al. (2013). Novel Artemisinin Derivatives with Potential Usefulness against Liver/colon Cancer and Viral Hepatitis. Bioorg. Med. Chem. 21 (14), 4432–4441. doi:10.1016/j.bmc.2013.04.059

PubMed Abstract | CrossRef Full Text | Google Scholar

Cai, Z., and Luo, Y. (2014). The Protective Effect and Mechanism of Emodin on Experimental Viral Myocarditis in Mice. Guangdong Medicial J. 35 (9), 1326–1329. doi:10.13820/j.cnki.gdyx.2014.09.012

Google Scholar

Chen, C., Li, X., Liu, Y., and Chen, S. (2021). Clinical Study of Lianhua Qingwen Capsule in the Treatment of Corona Virus Disease 2019. Res. Integrated Traditional Chin. West. Med. 13 (1), 1–4. doi:10.3969/j.issn.1674-4616.2021.01.001

Google Scholar

Chen, M., Li, H., Lu, X., Ling, L., Weng, H., Sun, W., et al. (2019). Houttuynia Cordata Polysaccharide Alleviated Intestinal Injury and Modulated Intestinal Microbiota in H1N1 Virus Infected Mice. Chin. J. Nat. Medicines 17 (3), 187–197. doi:10.1016/s1875-5364(19)30021-4

CrossRef Full Text | Google Scholar

Chen, T., and Huang, D. (1994). The Inhibitory Effect of Burdock on the Expression of Epstein-Barr Virus Antigen. Chin. J. Exp. Clin. Virol. 8 (4), 323–326.

Google Scholar

Chen, Y., Luo, Q., Li, S., Li, C., Liao, S., Yang, X., et al. (2020). Antiviral Activity against Porcine Epidemic Diarrhea Virus of Pogostemon Cablin Polysaccharide. J. Ethnopharmacology 259, 113009. doi:10.1016/j.jep.2020.113009

CrossRef Full Text | Google Scholar

Chen, Z., Wu, L. W., Liu, S. T., Cai, C. P., Rao, P. F., and Ke, L. J. (2006). Mechanism Study of Anti-influenza Effects of Radix Isatidis Water Extract by Red Blood Cells Capillary Electrophoresis. Zhongguo Zhong Yao Za Zhi 31 (20), 1715–1719. doi:10.3321/j.issn:1001-5302.2006.20.019

PubMed Abstract | Google Scholar

Cheng, D., Wang, W., Li, Y., Wu, X., Zhou, B., and Song, Q. (2020). Analysis of Curative Effect of 51 Patients with Novel Coronavirus Pneumonia Treated with Chinese Medicine Lianhua Qingwen:a Multicentre Retrospective Study. Tianjin Traditional Chin. Med. 37 (5), 509–516. doi:10.11656/j.issn.1672-1519.2020.05.06

Google Scholar

Cheng, K., Wu, Z., Gao, B., and Xu, J. (2014). Analysis of Influence of Baicalin Joint Resveratrol Retention Enema on the TNF-α, SIgA, IL-2, IFN-γ of Rats with Respiratory Syncytial Virus Infection. Cell Biochem Biophys. 70 (2), 1305–1309. doi:10.1007/s12013-014-0055-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Choi, H. J., Song, H.-H., Lee, J.-S., Ko, H.-J., and Song, J.-H. (2016). Inhibitory Effects of Norwogonin, Oroxylin A, and Mosloflavone on Enterovirus 71. Biomolecules Ther. (Seoul) 24 (5), 552–558. doi:10.4062/biomolther.2015.200

PubMed Abstract | CrossRef Full Text | Google Scholar

Chu, M., Xu, L., Zhang, M. B., Chu, Z. Y., and Wang, Y. D. (2015). Role of Baicalin in Anti-influenza Virus A as a Potent Inducer of IFN-Gamma. Biomed. Res. Int. 2015, 263630. doi:10.1155/2015/263630

PubMed Abstract | CrossRef Full Text | Google Scholar

Civitelli, L., Panella, S., Marcocci, M. E., De Petris, A., Garzoli, S., Pepi, F., et al. (2014). In vitro inhibition of Herpes Simplex Virus Type 1 Replication by Mentha Suaveolens Essential Oil and its Main Component Piperitenone Oxide. Phytomedicine 21 (6), 857–865. doi:10.1016/j.phymed.2014.01.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Dao, T. T., Nguyen, P. H., Lee, H. S., Kim, E., Park, J., Lim, S. I., et al. (2011). Chalcones as Novel Influenza A (H1N1) Neuraminidase Inhibitors from Glycyrrhiza Inflata. Bioorg. Med. Chem. Lett. 21 (1), 294–298. doi:10.1016/j.bmcl.2010.11.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Deng, L., Pang, P., Zheng, K., Nie, J., Xu, H., Wu, S., et al. (2016). Forsythoside A Controls Influenza A Virus Infection and Improves the Prognosis by Inhibiting Virus Replication in Mice. Molecules 21 (5). doi:10.3390/molecules21050524

PubMed Abstract | CrossRef Full Text | Google Scholar

Dias, M. M., Zuza, O., Riani, L. R., de Faria Pinto, P., Pinto, P. L. S., Silva, M. P., et al. (2017). In vitro schistosomicidal and Antiviral Activities of Arctium Lappa L. (Asteraceae) against Schistosoma Mansoni and Herpes Simplex Virus-1. Biomed. Pharmacother. 94, 489–498. doi:10.1016/j.biopha.2017.07.116

PubMed Abstract | CrossRef Full Text | Google Scholar

Ding, Y., Cao, Z., Cao, L., Ding, G., Wang, Z., and Xiao, W. (2017). Antiviral Activity of Chlorogenic Acid against Influenza A (H1N1/H3N2) Virus and its Inhibition of Neuraminidase. Sci. Rep. 7, 45723. doi:10.1038/srep45723

PubMed Abstract | CrossRef Full Text | Google Scholar

Duan, C., Xia, W., Zheng, Q., Sun, G., LI, Z., Li, Q., et al. (2020). Clinical Observation on Jinhua Qinggan Granule Combined with Conventional Western Medicine Therapy in Treating Mild Cases of Coronavirus Disease 2019. J. traditional Chin. Med. 61 (17), 1473–1477. doi:10.13288/j.11-2166/r.2020.17.001

Google Scholar

Esposito, F., Carli, I., Del Vecchio, C., Xu, L., Corona, A., Grandi, N., et al. (2016). Sennoside A, Derived from the Traditional Chinese Medicine Plant Rheum L., Is a New Dual HIV-1 Inhibitor Effective on HIV-1 Replication. Phytomedicine 23 (12), 1383–1391. doi:10.1016/j.phymed.2016.08.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Evers, D. L., Chao, C.-F., Wang, X., Zhang, Z., Huong, S.-M., and Huang, E.-S. (2005). Human Cytomegalovirus-Inhibitory Flavonoids: Studies on Antiviral Activity and Mechanism of Action. Antiviral Res. 68 (3), 124–134. doi:10.1016/j.antiviral.2005.08.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Fang, J., Tang, J., Yang, Z., Hu, Y., Liu, Y., and Wang, W. (2005). Effect of Radix Isatidis against Herpes Simplex Virus Type Ⅰ In Vitro. Chin. Traditional Herbal Drugs 36 (2), 242–244. doi:10.3321/j.issn:0253-2670.2005.02.034

Google Scholar

Fu, X., Wang, Z., Li, L., Dong, S., Li, Z., Jiang, Z., et al. (2016). Novel Chemical Ligands to Ebola Virus and Marburg Virus Nucleoproteins Identified by Combining Affinity Mass Spectrometry and Metabolomics Approaches. Sci. Rep. 6, 29680. doi:10.1038/srep29680

PubMed Abstract | CrossRef Full Text | Google Scholar

Galasiti Kankanamalage, A. C., Kim, Y., Damalanka, V. C., Rathnayake, A. D., Fehr, A. R., Mehzabeen, N., et al. (2018). Structure-guided Design of Potent and Permeable Inhibitors of MERS Coronavirus 3CL Protease that Utilize a Piperidine Moiety as a Novel Design Element. Eur. J. Med. Chem. 150, 334–346. doi:10.1016/j.ejmech.2018.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Gamblin, S. J., and Skehel, J. J. (2010). Influenza Hemagglutinin and Neuraminidase Membrane Glycoproteins. J. Biol. Chem. 285 (37), 28403–28409. doi:10.1074/jbc.r110.129809

PubMed Abstract | CrossRef Full Text | Google Scholar

Gaymard, A., Le Briand, N., Frobert, E., Lina, B., and Escuret, V. (2016). Functional Balance between Neuraminidase and Haemagglutinin in Influenza Viruses. Clin. Microbiol. Infect. 22 (12), 975–983. doi:10.1016/j.cmi.2016.07.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Guan, W.‐j., Ni, Z. Y., Hu, Y., Liang, W. H., Ou, C. Q., He, J., et al. (2020). Clinical Characteristics of 2019 Novel Coronavirus Infection in China. N. Engl. J. Med. 382 (18), 1708–1720. doi:10.1056/NEJMoa2002032

Guo, S., Bao, L., and Cui, X. (2016). Effects of Baicalin on Activity of Influenza A Virus RNA Polymerase by Silencing Host Factors PACT. Chin. J. Pharmacovigilance 13 (3), 129–131. doi:10.19803/j.1672-8629.2016.03.001

Google Scholar

Hayashi, K., Narutaki, K., Nagaoka, Y., Hayashi, T., and Uesato, S. (2010). Therapeutic Effect of Arctiin and Arctigenin in Immunocompetent and Immunocompromised Mice Infected with Influenza A Virus. Biol. Pharm. Bull. 33 (7), 1199–1205. doi:10.1248/bpb.33.1199

PubMed Abstract | CrossRef Full Text | Google Scholar

He, F., Liu, Q., Wei, F., Liu, Y., Xiong, H., Zhou, X., et al. (2013). Anti-viral Activity of Rhubarb Extract and Emodin in Rotavirus-Infected Cells. Chin. J. Viral Dis. 3 (2), 112–116. doi:10.16505/j.2095-0136.2013.02.005

Google Scholar

He, L., Fan, F., Hou, X., Wu, H., Wang, J., Xu, H., et al. (2017). 4(3H)-Quinazolone Regulates Innate Immune Signaling upon Respiratory Syncytial Virus Infection by Moderately Inhibiting the RIG-1 Pathway in RAW264.7 Cell. Int. Immunopharmacology 52, 245–252. doi:10.1016/j.intimp.2017.09.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Ho, T., Wu, S., Chen, J., Li, C., and Hsiang, C. (2007). Emodin Blocks the SARS Coronavirus Spike Protein and Angiotensin-Converting Enzyme 2 Interaction. Antiviral Res. 74 (2), 92–101. doi:10.1016/j.antiviral.2006.04.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Hu, K., Guan, W. J., Bi, Y., Zhang, W., Li, L., Zhang, B., et al. (2020). Efficacy and Safety of Lianhuaqingwen Capsules, a Repurposed Chinese Herb, in Patients with Coronavirus Disease 2019: A Multicenter, Prospective, Randomized Controlled Trial. Phytomedicine 85, 153242. doi:10.1016/j.phymed.2020.153242

PubMed Abstract | CrossRef Full Text | Google Scholar

Huang, C., Wang, Y., Li, X., Ren, L., Zhao, J., Hu, Y., et al. (2020). Clinical Features of Patients Infected with 2019 Novel Coronavirus in Wuhan, China. Lancet 395 (10223), 497–506. doi:10.1016/s0140-6736(20)30183-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Hung, P.-Y., Ho, B.-C., Lee, S.-Y., Chang, S.-Y., Kao, C.-L., Lee, S.-S., et al. (2015). Houttuynia Cordata Targets the Beginning Stage of Herpes Simplex Virus Infection. PLoS One 10 (2), e0115475. doi:10.1371/journal.pone.0115475

PubMed Abstract | CrossRef Full Text | Google Scholar

Izcovich, A., Siemieniuk, R., Bartoszko, J., Ge, L., Zeraatkar, D., Kum, E., et al. (2020). Adverse Effects of Remdesivir, Hydroxychloroquine, and Lopinavir/Ritonavir When Used for COVID-19: Systematic Review and Meta-Analysis of Randomized Trials. Preprint at https://www.medrxiv.org/content/10.1101/2020.11.16.20232876v1 (2020).

Ji, S., Li, R., Wang, Q., Miao, W.-j., Li, Z.-w., Si, L.-l., et al. (2015). Anti-H1N1 Virus, Cytotoxic and Nrf2 Activation Activities of Chemical Constituents from Scutellaria Baicalensis. J. Ethnopharmacology 176, 475–484. doi:10.1016/j.jep.2015.11.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Jia, W., Mao, S., Zhang, P., Yan, G., Jin, J., and Liu, Y. (2018). Study on Antiviral Effect of Lonicera Japonica Thumb Polysaccharide In Vivo. J. Liaoning Univ. Traditional Chin. Med. 20 (6), 25–27. doi:10.13194/j.issn.1673-842x.2018.06.007

Google Scholar

Jia, Y., Xu, R., Hu, Y., Zhu, T., Ma, T., Wu, H., et al. (2016). Anti-NDV Activity of Baicalin from a Traditional Chinese Medicine In Vitro. J. Vet. Med. Sci. 78 (5), 819–824. doi:10.1292/jvms.15-0572

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiang, J., Li, S., Li, M., and Xiang, J. (2005). Anti-viral Effects of Chinonin against HSV-Ⅱ In Vitro. Acta Medicinae Universitatis Scientiae Et Technologiae Huazhong 34 (3), 304–307.

Google Scholar

Jiang, J., and Xiang, J. (2004). Study on Activity of Chinonin against HSV-Ⅰ In Vitro. China Pharmacist 7 (9), 666–670. doi:10.3969/j.issn.1008-049X.2004.09.004

Google Scholar

Jiang, N., Liao, W., and Kuang, X. (2014). Effects of Emodin on IL-23/IL-17 Inflammatory axis, Th17 Cells and Viral Replication in Mice with Viral Myocarditis. Nan Fang Yi Ke Da Xue Xue Bao 34 (3), 373–378.

PubMed Abstract | Google Scholar

Jin, J., Chen, S., Wang, D., Chen, Y., Wang, Y., Guo, M., et al. (2018). Oroxylin A Suppresses Influenza A Virus Replication Correlating with Neuraminidase Inhibition and Induction of IFNs. Biomed. Pharmacother. 97, 385–394. doi:10.1016/j.biopha.2017.10.140

PubMed Abstract | CrossRef Full Text | Google Scholar

Jin, M., Ren, D., Meng, F., and Li, X. (2007). The Effects of Radix Isatidis on Immunological Function and Influenza Virus (FM1) in Kunming Mice. Lishizhen Med. Materia Med. Res. 18 (2), 394–396. doi:10.3969/j.issn.1008-0805.2007.02.073

Google Scholar

Kaufmann, S. H. E., Dorhoi, A., Hotchkiss, R. S., and Bartenschlager, R. (2018). Host-directed Therapies for Bacterial and Viral Infections. Nat. Rev. Drug Discov. 17 (1), 35–56. doi:10.1038/nrd.2017.162

PubMed Abstract | CrossRef Full Text | Google Scholar

Khider, L., Gendron, N., Goudot, G., Chocron, R., Hauw-Berlemont, C., Cheng, C., et al. (2020). Curative Anticoagulation Prevents Endothelial Lesion in COVID-19 Patients. J. Thromb. Haemost. 18, 2391-2399. doi:10.1111/jth.14968

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, M., Nguyen, D.-V., Heo, Y., Park, K. H., Paik, H.-D., and Kim, Y. B. (2020). Antiviral Activity of Fritillaria Thunbergii Extract against Human Influenza Virus H1N1 (PR8) In Vitro, in Ovo and In Vivo. J. Microbiol. Biotechnol. 30 (2), 172–177. doi:10.4014/jmb.1908.08001

PubMed Abstract | CrossRef Full Text | Google Scholar

Kitamura, K., Honda, M., Yoshizaki, H., Yamamoto, S., Nakane, H., Fukushima, M., et al. (1998). Baicalin, an Inhibitor of HIV-1 Production In Vitro. Antiviral Res. 37 (2), 131–140. doi:10.1016/s0166-3542(97)00069-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Ko, H.-C., Wei, B.-L., and Chiou, W.-F. (2006). The Effect of Medicinal Plants Used in Chinese Folk Medicine on RANTES Secretion by Virus-Infected Human Epithelial Cells. J. Ethnopharmacology 107 (2), 205–210. doi:10.1016/j.jep.2006.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Konoshima, T., Kokumai, M., Kozuka, M., Iinuma, M., Mizuno, M., Tanaka, T., et al. (1992). Studies on Inhibitors of Skin Tumor Promotion. XI. Inhibitory Effects of Flavonoides from Scutellaria Baicalensis on Epstein-Barr Virus Activation and Their Anti-tumor-promoting Activities. Chem. Pharm. Bull (Tokyo) 40 (2), 531–533. doi:10.1248/cpb.40.531

PubMed Abstract | CrossRef Full Text | Google Scholar

Korenaga, M., Hidaka, I., Nishina, S., Sakai, A., Shinozaki, A., Gondo, T., et al. (2011). A Glycyrrhizin-Containing Preparation Reduces Hepatic Steatosis Induced by Hepatitis C Virus Protein and Iron in Mice. Liver Int. 31 (4), 552–560. doi:10.1111/j.1478-3231.2011.02469.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Laconi, S., Madeddu, M. A., and Pompei, R. (2014). Autophagy Activation and Antiviral Activity by a Licorice Triterpene. Phytother. Res. 28 (12), 1890–1892. doi:10.1002/ptr.5189

PubMed Abstract | CrossRef Full Text | Google Scholar

Lam, T. L., Lam, M. L., Au, T. K. K., Ip, D. T. M., Ng, T. B., Fong, W. P., et al. (2000). A Comparison of Human Immunodeficiency Virus Type-1 Protease Inhibition Activities by the Aqueous and Methanol Extracts of Chinese Medicinal Herbs. Life Sci. 67 (23), 2889–2896. doi:10.1016/s0024-3205(00)00864-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Lau, K.-M., Lee, K.-M., Koon, C.-M., Cheung, C. S.-F., Lau, C.-P., Ho, H.-M., et al. (2008). Immunomodulatory and Anti-SARS Activities of Houttuynia Cordata. J. Ethnopharmacology 118 (1), 79–85. doi:10.1016/j.jep.2008.03.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Law, A. H.-Y., Yang, C. L.-H., Lau, A. S.-Y., and Chan, G. C.-F. (2017). Antiviral Effect of Forsythoside A from Forsythia Suspensa (Thunb.) Vahl Fruit against Influenza A Virus through Reduction of Viral M1 Protein. J. Ethnopharmacology 209, 236–247. doi:10.1016/j.jep.2017.07.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, Y.-R., Yeh, S.-F., Ruan, X.-M., Zhang, H., Hsu, S.-D., Huang, H.-D., et al. (2017). Honeysuckle Aqueous Extract and Induced Let-7a Suppress Dengue Virus Type 2 Replication and Pathogenesis. J. Ethnopharmacology 198, 109–121. doi:10.1016/j.jep.2016.12.049

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, H., Wu, J., Zhang, Z., Ma, Y., Liao, F., Zhang, Y., et al. (2011). Forsythoside a Inhibits the Avian Infectious Bronchitis Virus in Cell Culture. Phytother. Res. 25 (3), 338–342. doi:10.1002/ptr.3260

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, L., et al. (2017). Bioinformatics Analysis on Effect of Lonicerae Japonicae Flos and Forsythiae Fructus on Immune Pathway of H1N1 Influenza A. Chin. J. Exp. Traditional Med. Formulae 23 (10), 201–204.

Google Scholar

Li, S.-W., Yang, T.-C., Lai, C.-C., Huang, S.-H., Liao, J.-M., Wan, L., et al. (2014). Antiviral Activity of Aloe-Emodin against Influenza A Virus via Galectin-3 Up-Regulation. Eur. J. Pharmacol. 738, 125–132. doi:10.1016/j.ejphar.2014.05.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, T., Liu, L., Wu, H., Chen, S., Zhu, Q., Gao, H., et al. (2017b). Anti-herpes Simplex Virus Type 1 Activity of Houttuynoid A, a Flavonoid from Houttuynia Cordata Thunb. Antiviral Res. 144, 273–280. doi:10.1016/j.antiviral.2017.06.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, W., et al. (2019). Effect of Baicalin on Blood Index in Mice Infected H6 N6 Avian Influenza Virus. Chin. J. Vet. Drug 53 (10), 61–70.

Google Scholar

Li, X., Huang, Y., Sun, M., Ji, H., Dou, H., Hu, J., et al. (2018). Honeysuckle-encoded microRNA2911 Inhibits Enterovirus 71 Replication via Targeting VP1 Gene. Antiviral Res. 152, 117–123. doi:10.1016/j.antiviral.2018.02.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, X., Liu, Y., Wu, T., Jin, Y., Cheng, J., Wan, C., et al. (2015). The Antiviral Effect of Baicalin on Enterovirus 71 In Vitro. Viruses 7 (8), 4756–4771. doi:10.3390/v7082841

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, X., Yang, Y., Liu, L., Yang, X., Zhao, X., Li, Y., et al. (2020). Effect of Combination Antiviral Therapy on Hematological Profiles in 151 Adults Hospitalized with Severe Coronavirus Disease 2019. Pharmacol. Res. 160, 105036. doi:10.1016/j.phrs.2020.105036

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, Z., Li, L., Zhou, H., Zeng, L., Chen, T., Chen, Q., et al. (2017a). Radix Isatidis Polysaccharides Inhibit Influenza a Virus and Influenza A Virus-Induced Inflammation via Suppression of Host TLR3 Signaling In Vitro. Molecules 22 (1). doi:10.3390/molecules22010116

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, X., Huang, Y., Pan, X., Hao, Y., Chen, X., Jiang, H., et al. (2020). Erucic Acid from Isatis Indigotica Fort. Suppresses Influenza A Virus Replication and Inflammation In Vitro and In Vivo through Modulation of NF-Κb and P38 MAPK Pathway. J. Pharm. Anal. 10 (2), 130–146. doi:10.1016/j.jpha.2019.09.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Lin, T.-Y., Liu, Y.-C., Jheng, J.-R., Tsai, H.-P., Jan, J.-T., Wong, W.-R., et al. (2009). Anti-enterovirus 71 Activity Screening of Chinese Herbs with Anti-infection and Inflammation Activities. Am. J. Chin. Med. 37 (1), 143–158. doi:10.1142/s0192415x09006734

PubMed Abstract | CrossRef Full Text | Google Scholar

Lin, W., et al. (2020). Influence of Salidroside on Serum and Lung Tissue Inflammatory Factors and Immunological Indexes of Mice Infected with Influenza Virus. Chin. J. Nosocomiology 30 (2), 292–296.

Google Scholar

Ling, L.-j., Lu, Y., Zhang, Y.-y., Zhu, H.-y., Tu, P., Li, H., et al. (2020). Flavonoids from Houttuynia Cordata Attenuate H1N1-Induced Acute Lung Injury in Mice via Inhibition of Influenza Virus and Toll-like Receptor Signalling. Phytomedicine 67, 153150. doi:10.1016/j.phymed.2019.153150

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, F., et al. (2016a). Polyphenolic Glycosides Isolated from Pogostemon Cablin (Blanco) Benth. As Novel Influenza Neuraminidase Inhibitors. Chem. Cent. J. 10, 51. doi:10.1186/s13065-016-0192-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, L., Shi, F., Tu, P., Chen, C., Zhang, M., Li, X., et al. (2021). Arbidol Combined with the Chinese Medicine Lianhuaqingwen Capsule versus Arbidol Alone in the Treatment of COVID-19. Medicine (Baltimore) 100 (4), e24475. doi:10.1097/md.0000000000024475

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, M., Gao, Y., Yuan, Y., Yang, K., Shi, S., Zhang, J., et al. (2020). Efficacy and Safety of Integrated Traditional Chinese and Western Medicine for Corona Virus Disease 2019 (COVID-19): a Systematic Review and Meta-Analysis. Pharmacol. Res. 158, 104896. doi:10.1016/j.phrs.2020.104896

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, S., Yan, J., Xing, J., Song, F., Liu, Z., and Liu, S. (2012). Characterization of Compounds and Potential Neuraminidase Inhibitors from the N-Butanol Extract of Compound Indigowoad Root Granule Using Ultrafiltration and Liquid Chromatography-Tandem Mass Spectrometry. J. Pharm. Biomed. Anal. 59, 96–101. doi:10.1016/j.jpba.2011.10.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, X., Yang, Y., Zhou, T., Zhang, J., Yang, X., and Chen, H. (2002). The Effects of Astragalus Membranaceus, Rhodilolea and FTY720 on Murine Virus Mvocarditis Model Induced by Coxsackievirus B3. Mol. Cardiol. China 2 (3), 17–22.

Google Scholar

Liu, Y., et al. (2016b). Antiviral Effects of Three Chinese Herbal Medicine and Their Polysaccharides on Porcine Reproductive and Respiratory Syndrome Virus (PRRSV)In Vitro. China Anim. Husbandry Vet. Med. 43 (10), 2730–2735.

Google Scholar

Liu, Z., Li, X., Gou, C., Li, L., Luo, X., Zhang, C., et al. (2020b). Effect of Jinhua Qinggan Granules on Novel Coronavirus Pneumonia in Patients. J. Tradit Chin. Med. 40 (3), 467–472. doi:10.19852/j.cnki.jtcm.2020.03.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Z., Ma, N., Zhong, Y., and Yang, Z.-q. (2015). Antiviral Effect of Emodin from Rheum Palmatum against Coxsakievirus B5 and Human Respiratory Syncytial Virus In Vitro. J. Huazhong Univ. Sci. Technol. Med. Sci. 35 (6), 916–922. doi:10.1007/s11596-015-1528-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Lou, X., Hu, J., Ge, D., and Lu, W. (2017). Protective Effect of Honeysuckle on Viral Myocarditis in Mice and its Mechanism. J. Traditional Chin. Med. 45 (1), 37–41. doi:10.3969/j.issn.1002-2392.2017.01.010

Google Scholar

Lubbe, A., Seibert, I., Klimkait, T., and van der Kooy, F. (2012). Ethnopharmacology in Overdrive: the Remarkable Anti-HIV Activity of Artemisia Annua. J. Ethnopharmacology 141 (3), 854–859. doi:10.1016/j.jep.2012.03.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Luo, W., Su, X., and Gong, S. (2009). Anti-SARS Coronavirus 3C-like Protease Effects of Rheum Palmatum L. Extracts. Biosci. Trends 3 (4), 124–126. https://www.biosciencetrends.com/article/3/4/124

PubMed AbstractGoogle Scholar

Luo, Z., Liu, L. F., Wang, X. H., Li, W., Jie, C., Chen, H., et al. (2019). Epigoitrin, an Alkaloid from Isatis Indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model In Vivo and In Vitro. Front. Pharmacol. 10, 78. doi:10.3389/fphar.2019.00078

PubMed Abstract | CrossRef Full Text | Google Scholar

Lv, R., and Wang, W. L. X. (2020). Clinical Observation on Lianhua Qingwen Granules Combined with Western Medicine Conventional Therapy in the Treatment of 63 Suspected Cases of Coronavirus Disease 2019. J. Traditional Chin. Med. 6 (18), 655–659.

Google Scholar

Ma, P., et al. (2004). Study on Anti-Coxsackie Virus B3 Effect of Artemisinin. Chin. J. Endemiology 23 (5), 403–405.

Google Scholar

Mantani, N., Imanishi, N., Kawamata, H., Terasawa, K., and Ochiai, H. (2001). Inhibitory Effect of (+)-catechin on the Growth of Influenza A/PR/8 Virus in MDCK Cells. Planta Med. 67 (3), 240–243. doi:10.1055/s-2001-12009

PubMed Abstract | CrossRef Full Text | Google Scholar

Meo, S. A., Alhowikan, A. M., Al-Khlaiwi, T., Meo, I. M., Halepoto, D. M., Iqbal, M., et al. (2020). Novel Coronavirus 2019-nCoV: Prevalence, Biological and Clinical Characteristics Comparison with SARS-CoV and MERS-CoV. Eur. Rev. Med. Pharmacol. Sci. 24 (4), 2012–2019. doi:10.26355/eurrev_202002_20379

PubMed Abstract | CrossRef Full Text | Google Scholar

Michaelis, M., Sithisarn, P., and Cinatl Jr, J. (2014). Effects of Flavonoid-Induced Oxidative Stress on Anti-h5n1 Influenza a Virus Activity Exerted by Baicalein and Biochanin A. BMC Res. Notes 7, 384. doi:10.1186/1756-0500-7-384

PubMed Abstract | CrossRef Full Text | Google Scholar

Moisy, D., Avilov, S. V., Jacob, Y., Laoide, B. M., Ge, X., Baudin, F., et al. (2012). HMGB1 Protein Binds to Influenza Virus Nucleoprotein and Promotes Viral Replication. J. Virol. 86 (17), 9122–9133. doi:10.1128/jvi.00789-12

PubMed Abstract | CrossRef Full Text | Google Scholar

Nagai, T., Moriguchi, R., Suzuki, Y., Tomimori, T., and Yamada, H. (1995a). Mode of Action of the Anti-influenza Virus Activity of Plant Flavonoid, 5,7,4′-Trihydroxy-8-Methoxyflavone, from the Roots of Scutellaria Baicalensis. Antiviral Res. 26 (1), 11–25. doi:10.1016/0166-3542(94)00062-d

PubMed Abstract | CrossRef Full Text | Google Scholar

Nagai, T., Suzuki, Y., Tomimori, T., and Yamada, H. (1995b). Antiviral Activity of Plant Flavonoid, 5,7,4'-Trihydroxy-8-Methoxyflavone, from the Roots of Scutellaria Baicalensis against Influenza A (H3N2) and B Viruses. Biol. Pharm. Bull. 18 (2), 295–299. doi:10.1248/bpb.18.295

PubMed Abstract | CrossRef Full Text | Google Scholar

Nayak, M. K., Agrawal, A. S., Bose, S., Naskar, S., Bhowmick, R., Chakrabarti, S., et al. (2014). Antiviral Activity of Baicalin against Influenza Virus H1N1-Pdm09 Is Due to Modulation of NS1-Mediated Cellular Innate Immune Responses. J. Antimicrob. Chemother. 69 (5), 1298–1310. doi:10.1093/jac/dkt534

PubMed Abstract | CrossRef Full Text | Google Scholar

Oo, A., Rausalu, K., Merits, A., Higgs, S., Vanlandingham, D., Bakar, S. A., et al. (2018). Deciphering the Potential of Baicalin as an Antiviral Agent for Chikungunya Virus Infection. Antiviral Res. 150, 101–111. doi:10.1016/j.antiviral.2017.12.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Orzechowska, B., Chaber, R., Wiśniewska, A., Pajtasz-Piasecka, E., Jatczak, B., Siemieniec, I., et al. (2014). Baicalin from the Extract of Scutellaria Baicalensis Affects the Innate Immunity and Apoptosis in Leukocytes of Children with Acute Lymphocytic Leukemia. Int. Immunopharmacology 23 (2), 558–567. doi:10.1016/j.intimp.2014.10.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Ou, C., Zhang, Q., Wu, G., Shi, N., and He, C. (2015). Dryocrassin ABBA, a Novel Active Substance for Use against Amantadine-Resistant H5N1 Avian Influenza Virus. Front. Microbiol. 6, 592. doi:10.3389/fmicb.2015.00592

PubMed Abstract | CrossRef Full Text | Google Scholar

Pang, P., Zheng, K., Wu, S., Xu, H., Deng, L., Shi, Y., et al. (2018). Baicalin Downregulates RLRs Signaling Pathway to Control Influenza A Virus Infection and Improve the Prognosis. Evid. Based Complement. Alternat Med. 2018, 4923062. doi:10.1155/2018/4923062

PubMed Abstract | CrossRef Full Text | Google Scholar

Penarrubia, A. L., Ruiz, M., Porco, R., Rao, S. N., Vella, S. A., Juanola-Falgarona, M., et al. (2020). Multiple Assays in a Real-Time RT-PCR SARS-CoV-2 Panel Can Mitigate the Risk of Loss of Sensitivity by New Genomic Variants during the COVID-19 Outbreak. Int. J. Infect. Dis. 97, 225-229. doi:10.1016/j.ijid.2020.06.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Pillaiyar, T., Manickam, M., Namasivayam, V., Hayashi, Y., and Jung, S. -H. (2016). An Overview of Severe Acute Respiratory Syndrome-Coronavirus (SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule Chemotherapy. J. Med. Chem. 59 (14), 6595–6628. doi:10.1021/acs.jmedchem.5b01461

PubMed Abstract | CrossRef Full Text | Google Scholar

Qaseem, A., Yost, J., Etxeandia-Ikobaltzeta, I., Abraham, G. M., Jokela, J. A., Forciea, M. A., et al. (2021). Should Remdesivir Be Used for the Treatment of Patients with COVID-19? Rapid, Living Practice Points from the American College of Physicians (Version 2). Ann. Intern. Med. M208101. doi:10.7326/m20-8101

CrossRef Full Text | Google Scholar

Qiao, Y., Fang, J.-g., Xiao, J., Liu, T., Liu, J., Zhang, Y.-l., et al. (2013). Effect of Baicalein on the Expression of VIP in Extravillous Cytotrophoblasts Infected with Human Cytomegalovirus In Vitro. J. Huazhong Univ. Sci. Technol. Med. Sci. 33 (3), 406–411. doi:10.1007/s11596-013-1132-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Qu, X.-y., Li, Q.-j., Zhang, H.-m., Zhang, X.-j., Shi, P.-h., Zhang, X.-j., et al. (2016). Protective Effects of Phillyrin against Influenza A Virus In Vivo. Arch. Pharm. Res. 39 (7), 998–1005. doi:10.1007/s12272-016-0775-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Ren, X. H., Qi, X., Zuo, Q., Tang, J., and Liu, D. (2020). Analysis of Treatment of 813 COVID-19 Patients in the Fangcang Hospital. Med. Guide 39 (07), 926–930. doi:10.3870/j.issn.1004-0781.2020.07.008

Google Scholar

Roy, S., He, R., Kapoor, A., Forman, M., Mazzone, J. R., Posner, G. H., et al. (2015). Inhibition of Human Cytomegalovirus Replication by Artemisinins: Effects Mediated through Cell Cycle Modulation. Antimicrob. Agents Chemother. 59 (7), 3870–3879. doi:10.1128/aac.00262-15

PubMed Abstract | CrossRef Full Text | Google Scholar

Runfeng, L., Yunlong, H., Jicheng, H., Weiqi, P., Qinhai, M., Yongxia, S., et al. (2020). Lianhuaqingwen Exerts Anti-viral and Anti-inflammatory Activity against Novel Coronavirus (SARS-CoV-2). Pharmacol. Res. 156, 104761. doi:10.1016/j.phrs.2020.104761

PubMed Abstract | CrossRef Full Text | Google Scholar

Seong, R.-K., Kim, J.-A., and Shin, O. S. (2018). Wogonin, a Flavonoid Isolated from Scutellaria Baicalensis, Has Anti-viral Activities against Influenza Infection via Modulation of AMPK Pathways. Acta Virol. 62 (1), 78–85. doi:10.4149/av_2018_109

PubMed Abstract | CrossRef Full Text | Google Scholar

Shen, C., Zhang, Z., and Xie, T. (2020). Rhein Suppresses Lung Inflammatory Injury Induced by Human Respiratory Syncytial Virus through Inhibiting NLRP3 Inflammasome Activation via NF-Κb Pathway in Mice. Front. Pharmacol. 10, 1600. doi:10.3389/fphar.2019.01600

PubMed Abstract | CrossRef Full Text | Google Scholar

Shi, C.-c., Zhu, H.-y., Li, H., Zeng, D.-l., Shi, X.-l., Zhang, Y.-y., et al. (2020). Regulating the Balance of Th17/Treg Cells in Gut-Lung axis Contributed to the Therapeutic Effect of Houttuynia Cordata Polysaccharides on H1N1-Induced Acute Lung Injury. Int. J. Biol. Macromolecules 158, 52–66. doi:10.1016/j.ijbiomac.2020.04.211

CrossRef Full Text | Google Scholar

Sithisarn, P., Michaelis, M., Schubert-Zsilavecz, M., and Cinatl, J., Jr. (2013). Differential Antiviral and Anti-inflammatory Mechanisms of the Flavonoids Biochanin A and Baicalein in H5N1 Influenza A Virus-Infected Cells. Antiviral Res. 97 (1), 41–48. doi:10.1016/j.antiviral.2012.10.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Swarup, V., Ghosh, J., Mishra, M. K., and Basu, A. (2008). Novel Strategy for Treatment of Japanese Encephalitis Using Arctigenin, a Plant Lignan. J. Antimicrob. Chemother. 61 (3), 679–688. doi:10.1093/jac/dkm503

PubMed Abstract | CrossRef Full Text | Google Scholar

Trivedi, A., Sharma, S., and Ashtey, B. (2020). Investigational Treatments for COVID-19. Pharm. J. 304 (7938). doi:10.1211/PJ.2020.20208051

Google Scholar

Walls, A. C., Park, Y.-J., Tortorici, M. A., Wall, A., McGuire, A. T., and Veesler, D. (2020). Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein. Cell 181 (2), 281–292. doi:10.1016/j.cell.2020.02.058

PubMed Abstract | CrossRef Full Text | Google Scholar

Wan, Q., et al. (2015). Effects of Baicalin on ET-1 and its Receptors of Pneumonia Mice Lung Tissue Infected with Influenza A Virus. Chin. J. Traditional Chin. Med. Pharm. 30 (4), 1290–1293.

Google Scholar

Wan, Q., Wang, H., Han, X., Lin, Y., Yang, Y., Gu, L., et al. (2014). Baicalin Inhibits TLR7/MYD88 Signaling Pathway Activation to Suppress Lung Inflammation in Mice Infected with Influenza A Virus. Biomed. Rep. 2 (3), 437–441. doi:10.3892/br.2014.253

PubMed Abstract | CrossRef Full Text | Google Scholar

Wan, S., Yi, Q., Fan, S., Lv, J., Zhang, X., Guo, L., et al. (2020). Characteristics of Lymphocyte Subsets and Cytokines in Peripheral Blood of 123 Hospitalized Patients with 2019 Novel Coronavirus Pneumonia (NCP). Preprint at https://www.medrxiv.org/content/10.1101/2020.02.10.20021832v1 (2020).

Wang, H., Ding, Y., Zhou, J., Sun, X., and Wang, S. (2009a). The In Vitro and In Vivo Antiviral Effect of Salidroside and its Analogue against Coxsackievirus B3. Chin. J. Hosp. Pharm. 29 (18), 1514–1518.

Google Scholar

Wang, J., Chen, X., Wang, W., Zhang, Y., Yang, Z., Jin, Y., et al. (2013). Glycyrrhizic Acid as the Antiviral Component of Glycyrrhiza Uralensis Fisch. Against Coxsackievirus A16 and Enterovirus 71 of Hand Foot and Mouth Disease. J. Ethnopharmacology 147 (1), 114–121. doi:10.1016/j.jep.2013.02.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Wang, Y., Ye, D., and Liu, Q. (2020b). Review of the 2019 Novel Coronavirus (SARS-CoV-2) Based on Current Evidence. Int. J. Antimicrob. Agents 55 (6), 105948. doi:10.1016/j.ijantimicag.2020.105948

CrossRef Full Text | Google Scholar

Wang, M.-J., Yang, C.-H., Jin, Y., Wan, C.-B., Qian, W.-H., Xing, F., et al. (2020c). Baicalin Inhibits Coxsackievirus B3 Replication by Reducing Cellular Lipid Synthesis. Am. J. Chin. Med. 48 (1), 143–160. doi:10.1142/s0192415x20500081

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Q.-W., Su, Y., Sheng, J.-T., Gu, L.-M., Zhao, Y., Chen, X.-X., et al. (2018). Anti-influenza A Virus Activity of Rhein through Regulating Oxidative Stress, TLR4, Akt, MAPK, and NF-Κb Signal Pathways. PLoS One 13 (1), e0191793. doi:10.1371/journal.pone.0191793

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, S.-Y., Tseng, C.-P., Tsai, K.-C., Lin, C.-F., Wen, C.-Y., Tsay, H.-S., et al. (2009b). Bioactivity-guided Screening Identifies Pheophytin a as a Potent Anti-hepatitis C Virus Compound from Lonicera Hypoglauca Miq. Biochem. Biophysical Res. Commun. 385 (2), 230–235. doi:10.1016/j.bbrc.2009.05.043

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, T., Wang, X., Zhuo, Y., Si, C., Yang, L., Meng, L., et al. (2020a). Antiviral Activity of a Polysaccharide from Radix Isatidis (Isatis Indigotica Fortune) against Hepatitis B Virus (HBV) In Vitro via Activation of JAK/STAT Signal Pathway. J. Ethnopharmacology 257, 112782. doi:10.1016/j.jep.2020.112782

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, W., Xu, S., Guo, K., Xu, J., Cheng, G., Yu, J., et al. (2010). Effects of Herba Agastachis Essential Oil and Cortex Phellodendri Alkaloid on the Antioxidation of IEC-6 in High-Temperature. Chin. J. Vet. Med. 46 (7), 60–64. doi:10.3969/j.issn.0529-6005.2010.07.028

Google Scholar

Wei, W., Du, H., and Shao, C. (2019). Screening of Antiviral Components of Ma Huang Tang and Investigation on the Ephedra Alkaloids Efficacy on Influenza Virus Type A. Front. Pharmacol. 10, 961. doi:10.3389/fphar.2019.00961

PubMed Abstract | CrossRef Full Text | Google Scholar

Wei, X., Peng, C., and Wan, F. (2013). Study on the Inhibitory Effect of Anti-respiratory Viruses and Toxicity of Patchouli Alcohol In Vitro. Pharmacol. Clin. Chin. Materia Med. 29 (1), 26–29. doi:10.13412/j.cnki.zyyl.2013.01.010

Google Scholar

Wei, Z.-Y., Wang, X.-B., Zhang, H.-Y., Yang, C.-H., Wang, Y.-B., Xu, D.-H., et al. (2011). Inhibitory Effects of Indigowoad Root Polysaccharides on Porcine Reproductive and Respiratory Syndrome Virus Replication In Vitro. Antivir. Ther. 16 (3), 357–363. doi:10.3851/imp1755

PubMed Abstract | CrossRef Full Text | Google Scholar

Wolkerstorfer, A., Kurz, H., Bachhofner, N., and Szolar, O. H. (2009). Glycyrrhizin Inhibits Influenza A Virus Uptake into the Cell. Antiviral Res. 83 (2), 171–178. doi:10.1016/j.antiviral.2009.04.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, Y., Jin, Y., Wu, J., Yu, X., and Hao, Y. (2011). Effects of Wogonin on Inflammation-Related Factors in Alveolar Macrophages Infected with Influenza Virus. Chin. J. Pathophysiology 27 (3), 533–538. doi:10.3969/j.issn.1000-4718.2011.03.022

Google Scholar

Xiao, M., Tian, J., Zhou, Y., Xu, X., Min, X., Lv, Y., et al. (2020). Efficacy of Huoxiang Zhengqi Dropping Pills and Lianhua Qingwen Granules in Treatment of COVID-19: A Randomized Controlled Trial. Pharmacol. Res. 161, 105126. doi:10.1016/j.phrs.2020.105126

PubMed Abstract | CrossRef Full Text | Google Scholar

Xiao, P., Ye, W., Chen, J., and Li, X. (2016). Antiviral Activities against Influenza Virus (FM1) of Bioactive Fractions and Representative Compounds Extracted from Banlangen (Radix Isatidis). J. Tradit Chin. Med. 36 (3), 369–376. doi:10.1016/s0254-6272(16)30051-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, H., He, L., Chen, J., Hou, X., Fan, F., Wu, H., et al. (2019). Different Types of Effective Fractions from Radix Isatidis Revealed a Multiple-Target Synergy Effect against Respiratory Syncytial Virus through RIG-I and MDA5 Signaling Pathways, a Pilot Study to Testify the Theory of Superposition of Traditional Chinese Medicine Efficacy. J. Ethnopharmacology 239, 111901. doi:10.1016/j.jep.2019.111901

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, Y., Sun, J., and He, S. (2010). Effect of Three Kinds of Radix Isatidis Preparation on the Expression of Nucleoprotein of Influenza Virus. Shandong Med. J. 50 (27), 8–10.

Google Scholar

Yang, G., et al. (2010). Study on Inhibitory Effect of Five Kinds of Traditional Chinesel Medicine Including Dryopteris Crassirhizoma on Influenza A Virus FM1 Strain. J. Pract. Traditional Chin. Intern. Med. 24 (7), 3–4.

Google Scholar

Yang, Q., Gao, L., Si, J., Sun, Y., Liu, J., Cao, L., et al. (2013). Inhibition of Porcine Reproductive and Respiratory Syndrome Virus Replication by Flavaspidic Acid AB. Antiviral Res. 97 (1), 66–73. doi:10.1016/j.antiviral.2012.11.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Yeh, C., Wang, K. C., Chiang, L. C., Shieh, D. E., Yen, M. H., and Chang, J. (2013). Water Extract of Licorice Had Anti-viral Activity against Human Respiratory Syncytial Virus in Human Respiratory Tract Cell Lines. J. Ethnopharmacol 148 (2), 466–473.

PubMed AbstractGoogle Scholar

Yu, H., et al. (2020a). Efficacy Study of Arbidol, Qingfei Paidu Decoction, Lianhua Qingwen Capsule, and Jinye Baidu Granules in the Treatment of Mild/moderate COVID-19 in a Fangcang Shelter Hospital. Pharmacol. Clin. Chin. materia Med. 36 (6), 2–6.

Google Scholar

Yu, P., et al. (2020b). Effects of Lianhua Qingwen Granules Plus Arbidol on Treatment of Mild Corona Virus Disease-19. Chin. Pharm. J. 55 (12), 1042–1045.

Google Scholar

Zhang, L., et al. (2017). Effect of Active Extracts from Radix Isatidis against Respiratory Syncytial Virus In Vitro. Liaoning J. Traditional Chin. Med. 44 (5), 1007–1011.

Google Scholar

Zhang, P., et al. (2018). Effect of Baicalin on the Expression of Type I Interferon and SOCS1/3 in Rats Infected with Respiratory Syncytial Virus. Chin. J. Traditional Chin. Med. 33 (01), 328–332.

Google Scholar

Zhang, Q., Cao, F., Wang, Y., Xu, X., Sun, Y., Li, J., et al. (2020). The Efficacy and Safety of Jinhua Qinggan Granule (JHQG) in the Treatment of Coronavirus Disease 2019 (COVID-19). Medicine (Baltimore) 99 (24), e20531. doi:10.1097/md.0000000000020531

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, Y., Liu, X., and Liu, X. (2009). Anti-Coxsackievirus B3 Effects of Rhodiola Sachalinensis Polysaccaride In Vitro. Chin. J. Hosp. Pharm. 29 (20), 1749–1753.

Google Scholar

Zhang, Y., Wang, H., Liu, Y., Wang, C., Wang, J., Long, C., et al. (2018). Baicalein Inhibits Growth of Epstein-Barr Virus-Positive Nasopharyngeal Carcinoma by Repressing the Activity of EBNA1 Q-Promoter. Biomed. Pharmacother. 102, 1003–1014. doi:10.1016/j.biopha.2018.03.114

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, X., Zheng, M., Zhu, Z., Zheng, L., Qiu, B., Cao, H., et al. (2014). In Vitro Anti-respiratory Syncytial Virus Effect of the Extraction of Lonicera japonica Thunb. J. New Chinese Med. 46 (6), 204–206. doi:10.13457/j.cnki.jncm.2014.06.097

PubMed Abstract | CrossRef Full Text | Google Scholar

Zheng, W. K. (2020). SARS-CoV-2 Infection of Respiratory Tract. J. Traditional Chin. Med., 1–5.

Google Scholar

Zhi, H.-J., Zhu, H.-Y., Zhang, Y.-Y., Lu, Y., Li, H., and Chen, D.-F. (2019). In vivo effect of Quantified Flavonoids-Enriched Extract of Scutellaria Baicalensis Root on Acute Lung Injury Induced by Influenza A Virus. Phytomedicine 57, 105–116. doi:10.1016/j.phymed.2018.12.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhong, T., Zhang, L.-y., Wang, Z.-y., Wang, Y., Song, F.-m., Zhang, Y.-h., et al. (2017). Rheum Emodin Inhibits Enterovirus 71 Viral Replication and Affects the Host Cell Cycle Environment. Acta Pharmacol. Sin 38 (3), 392–401. doi:10.1038/aps.2016.110

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhou, L., et al. (2017). Mechanism Study of Houttuynia Cordata Anti-herpes Simplex Virus. China Feed (10), 10–16.

Google Scholar

Zhou, Z., Li, X., Liu, J., Dong, L., Chen, Q., Liu, J., et al. (2015). Honeysuckle-encoded Atypical microRNA2911 Directly Targets Influenza A Viruses. Cell Res. 25 (1), 39–49. doi:10.1038/cr.2014.130

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, H., Lu, X., Ling, L., Li, H., Ou, Y., Shi, X., et al. (2018). Houttuynia Cordata Polysaccharides Ameliorate Pneumonia Severity and Intestinal Injury in Mice with Influenza Virus Infection. J. Ethnopharmacology 218, 90–99. doi:10.1016/j.jep.2018.02.016

CrossRef Full Text | Google Scholar

Zhu, M., Mao, S., Liu, Y., Wang, L., Chen, T., Qin, L., et al. (2016). Study on the Antiviral Effect of Lonicera Japonica Water Decoction on Influenza Virus. Chin. Med. Mod. Distance Education China 14 (9), 135–137. doi:10.3969/j.issn.1672-2779.2016.09.059

Google Scholar

Zhu, X., and Li, W. (2012). Study on the Antiviral Activity of Water Extract of Ephedra Sinica against Respiratory Syncytial Virus Infection In Vitro. Pract. Prev. Med. 19 (10), 1555–1557. doi:10.3969/j.issn.1006-3110.2012.10.044

Google Scholar

Zumla, A., Hui, D. S., Azhar, E. I., Memish, Z. A., and Maeurer, M. (2020). Reducing Mortality from 2019-nCoV: Host-Directed Therapies Should Be an Option. The Lancet 395 (10224), e35–e36. doi:10.1016/s0140-6736(20)30305-6

CrossRef Full Text | Google Scholar

Zumla, A., Rao, M., Wallis, R. S., Kaufmann, S. H., Rustomjee, R., Mwaba, P., et al. (2015). Towards Host-Directed Therapies for Tuberculosis. Nat. Rev. Drug Discov. 14 (8), 511–512. doi:10.1038/nrd4696

PubMed Abstract | CrossRef Full Text | Google Scholar

Zuo, Y., Dai, M., Wang, Z., and Liu, J. (2008). Effects of Banlangen Polysaccharide on Mice Resistance to Influenza Virus Infection. West China J. Pharm. Sci. 23 (6), 666–667. doi:10.3969/j.issn.1006-0103.2008.06.015

Google Scholar

Keywords: broad-spectrum antivirals, Lian-Hua-Qing-Wen capsule, Jin-Hua-Qing-Gan granule, medicinal plants, COVID-19, SARS-CoV-2, host-directed therapy

Citation: Shi M, Peng B, Li A, Li Z, Song P, Li J, Xu R and Li N (2021) Broad Anti-Viral Capacities of Lian-Hua-Qing-Wen Capsule and Jin-Hua-Qing-Gan Granule and Rational use Against COVID-19 Based on Literature Mining. Front. Pharmacol. 12:640782. doi: 10.3389/fphar.2021.640782

Received: 12 December 2020; Accepted: 14 April 2021;
Published: 14 May 2021.

Edited by:

Maria De Lourdes Pereira, University of Aveiro, Portugal

Reviewed by:

Mahaveer Dhobi, Delhi Pharmaceutical Sciences and Research University, India
Bhoomika M. Patel, Nirma University, India
Sunil Kayesth, University of Delhi, India

Copyright © 2021 Shi, Peng, Li, Li, Song, Li, Xu and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ning Li, bGlsaS5saS5uaW5nQGdtYWlsLmNvbQ==; Ruodan Xu, cnVvZGFueHVAZ21haWwuY29t; Jing Li, bmF0YXNoYWxlZUAxNjMuY29t

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.