Skip to main content

ORIGINAL RESEARCH article

Front. Med., 29 April 2022
Sec. Infectious Diseases: Pathogenesis and Therapy

Listeriosis in a Metropolitan Hospital: Is Targeted Therapy a Risk Factor for Infection?

\nFanfan XingFanfan Xing1Simon K. F. LoSimon K. F. Lo1Susanna K. P. LauSusanna K. P. Lau2Patrick C. Y. Woo
Patrick C. Y. Woo2*
  • 1Department of Clinical Microbiology and Infection Control, The University of Hong Kong - Shenzhen Hospital, Shenzhen, China
  • 2Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China

Targeted therapies are widely used for treatment of autoimmune diseases as well as solid organ and hematological malignancies. Various opportunistic infections have been described in patients on targeted therapies. Although case reports or a few case series of listeriosis have been reported to be associated with targeted therapy, most of the cases were related to anti-tumor necrosis factor-α monoclonal antibody. In this study, we describe the epidemiological and clinical profiles of listeriosis in a tertiary hospital in Shenzhen, a Southern Chinese metropolitan city in China. During the 9-year-and-6-month study period, a total of five cases of listeriosis were recorded and all of them had Listeria monocytogenes bacteremia. All five patients had predisposing factors, including corticosteroid (n = 3), targeted therapy (n = 2), pregnancy (n = 2) and anti-interferon gamma autoantibody (n = 1). The two patients who had targeted therapy during their course of cancer treatment received inhibitors of the epidermal growth factor receptor (EGFR)/human epidermal growth factor receptor 2 (HER2) pathway. The first one was a 52-year-old woman with metastatic adenocarcinoma of the lung. She was given gefitinib (EGFR tyrosine kinase inhibitor), osimertinib (third-generation EGFR tyrosine kinase inhibitor) and afatinib (tyrosine kinase inhibitor that can bind to EGFR, HER2 and HER4). The second one was a 40-year-old woman with carcinoma of the breast with brain metastasis. She was given trastuzumab (anti-HER2 monoclonal antibody) and lapatinib (dual tyrosine kinase inhibitor of the EGFR/HER2 pathway). These two patients represent the second and third reports of listeria infections associated with EGFR/HER2 pathway inhibitors in the literature. Targeted therapy is an important predisposing factor for listeriosis. Listeria infection is an important differential diagnosis in patients on targeted therapy who present with sepsis and/or central nervous system infection, and the use of antibiotic regimens that cover listeria is crucial for empirical treatment. Avoidance of high-risk food items in these patients is important for the prevention of listeriosis.

Introduction

Listeriosis is a food-borne disease caused by Listeria monocytogenes or Listeria ivanovii, often due to ingestion of unpasteurized milk and dairy products as well as contaminated undercooked meat, ice-cream, salads, and other ready-to-eat items. However, in a significant proportion of patients, the contaminated food source may not be obvious. In immunocompetent hosts, listeriosis usually manifests as a self-limiting febrile gastroenteritis. Nevertheless, in patients of extreme age, pregnant women, and other immunodeficiency states, it may lead to systemic sepsis with bacteremia, disseminated abscesses in multiple organs especially liver and spleen, and most severely central nervous system infections including meningitis, rhombencephalitis, cerebritis and brain abscess. As L. monocytogenes and L. ivanovii are intracellular pathogens, the immunocompromised patients with listeriosis are often those with cell-mediated immunity defects, such as patients receiving corticosteroids, transplant recipients, and HIV carriers.

Targeted therapies are widely used for treatment of various kinds of autoimmune diseases as well as solid organ and hematological malignancies. Since the targets of such therapies are usually major players of immunological pathways, they are often associated with infectious diseases that require the particular type of immune response for control. Various opportunistic infections have been described to be associated with different targeted therapies, the commonest reported ones being tuberculosis and invasive fungal infections (14). Although case reports or a few case series of listeriosis have been reported to be associated with targeted therapy, most of the cases were related to anti-tumor necrosis factor-α (anti-TNFα) monoclonal antibody (536). Recently, we described the first report of L. monocytogenes bacteremia and severe sepsis complicating carfilzomib (proteosome inhibitor) and daratumumab (anti-CD38 monoclonal antibody) treatment for multiple myeloma (37). In this study, we describe the epidemiology and clinical course of listeria infections in a tertiary hospital in Shenzhen, a Southern Chinese metropolitan city with a large immigrant population from other parts of China. The importance of targeted therapy as a risk factor of listeriosis is also discussed.

Materials and Methods

Patients

This was a retrospective study conducted over a nine-year-and-six-month period (1 July 2012 to 31 December 2021) in The University of Hong Kong - Shenzhen Hospital. Many newer medications, which have not been registered or come into the market in mainland China, are available in Shenzhen Hospital of the University of Hong Kong. The clinical details, laboratory data and radiological findings of all patients with listeriosis were retrieved from the hospital electronic record system and were analyzed. Ethics approval for this study was provided by the Institutional Review Board of The University of Hong Kong - Shenzhen Hospital ([2022]041).

Microbiological Methods

Clinical specimens were collected and handled according to standard protocols, and all suspect colonies were identified by standard conventional biochemical method (38). The BacT/ALERT 3D(240) blood culture system (Becton Dickinson, Maryland, USA) was used. L. monocytogenes was suspected when facultative anaerobic Gram-positive non-sporulating rods with tumbling motility at room temperature were isolated on sheep blood agar. All identifications were confirmed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry by the direct transfer method using the MALDI–TOF MS spectrometer (Bruker Daltonik) and spectra analyzed with IVD MALDI Biotyper 2.3 and reference library DB-9607 (Bruker Daltonik) (39). In vitro susceptibility in terms of minimal inhibitory concentrations of penicillin on the L. monocytogenes strains was performed using Epsilometer-test (Liofilchem®), with quality control strain Streptococcus pneumoniae ATCC49619 as the reference strain.

Results

Epidemiology of Lsteriosis

During the study period, a total of five cases of listeriosis were recorded (Table 1). One patient was a male and the other four were females. Median age was 40 years (range: 27–59 years). All five patients had predisposing factors for listeriosis, including corticosteroid (n = 3), targeted therapy (n = 2), pregnancy (n = 2) and anti-interferon gamma autoantibody (n = 1). Two patients had consumed suspected food items which may be the source of the infection. Case 3 had eaten leftover meat and vegetable stored in the refrigerator for a few days, whereas case 4 had bird's nest which had also been stored in the refrigerator for 6 days.

TABLE 1
www.frontiersin.org

Table 1. Patients with listeriosis in the present cohort.

Clinical Course and Outcome

Case 1 was diagnosed to have metastatic adenocarcinoma of the lung in 2014. She was given gefitinib from November 2014 to October 2015, osimertinib from October 2015 to October 2016, and pemetrexed and cisplatinum from November 2016 to April 2017. Due to severe headache, she was admitted in June 2017 for brain radiotherapy. On admission, the total white cell count and neutrophils were within normal range, but lymphocytes were 0.87 × 109/L. Liver and renal function tests were normal. C-reaction protein was <5 mg/L. After admission, dexamethasone and whole brain radiotherapy were commenced. 25 days after admission, she developed urinary incontinence, bilateral lower limb weakness and coma. 2 days later, she started to have fever but there were no localizing signs. The total white cell count and neutrophils were elevated to 10.31 × 109/L and 9.33 × 109/L, respectively, and lymphocytes were decreased to 0.51 × 109/L. Liver and renal function tests remained normal. C-reaction protein was elevated to 67.9 mg/L. Then, Afatinib was commenced. On the next day, blood culture was collected but unfortunately the patient succumbed. 2 days later, blood culture yielded a Gram-positive bacillus, which was subsequently identified as L. monocytogenes.

Case 2 was diagnosed to have carcinoma of the breast with brain metastasis in April 2018. She was given paclitaxel, cisplatinum, trastuzumab and lapatinib from April to October 2018. Due to right upper limb weakness, oral dexamethasone was started in October 2018. 1 week after the commencement of dexamethasone, she was admitted for whole brain radiotherapy. On admission, she had fever without localizing symptoms or signs. The total white cell count and neutrophils were normal, but lymphocytes and platelet were 0.43 × 109/L and 56 × 109/L, respectively. Liver function test was mildly deranged. Renal function test was normal. Blood culture was performed and a Gram-positive bacillus was isolated from blood culture after 17 hours of incubation. The bacterium was subsequently identified as L. monocytogenes. The minimum inhibitory concentration of penicillin was 0.25 μg/mL. High dose intravenous ampicillin and gentamicin were commenced. Magnetic resonance imaging of the brain showed multiple metastatic lesions in the cerebrum, cerebellum and brainstem. Lumbar puncture was not performed because of the low platelet count. She became afebrile 3 days later and the antibiotics were kept for a total of 21 days.

Case 3 was diagnosed to have systemic lupus erythematosus and autoimmune hepatitis in 2015 and she had been put on prednisone and hydroxychloroquine since then. At her 19th week of gestation, she was admitted in March 2019 because of fever, chills and headache for 5 days. There were no localizing features. The total white cell count and neutrophils were elevated to 21.2 × 109/L and 17.8 × 109/L, respectively. Liver and renal function tests were normal. C-reactive protein was elevated at 40 mg/L. Blood culture was performed and empirical intravenous meropenem was commenced. Spontaneous abortion developed 2 days after admission. On the same day, blood culture yielded a Gram-positive bacillus, which was subsequently identified as L. monocytogenes. Contrast-enhanced computed tomography of the brain did not reveal any abnormality. Lumbar puncture was refused by the patient. Then, meropenem was stopped and intravenous ampicillin was commenced. She became afebrile 3 days later and antibiotics were kept for a total of 17 days.

Case 4 was diagnosed to have Sjögren's syndrome in November 2018 and she had been put on prednisone and hydroxychloroquine since then. Hydroxychloroquine was also added in March 2019. At her 29th week of gestation, she was admitted in August 2019 because of fever, chills, rigor and absence of fetal movement for 3 days. There were no localizing features. The total white cell count and neutrophils were elevated to 17.0 × 109/L and 13.7 × 109/L, respectively. Liver and renal function tests were normal. C-reactive protein levels were high (93.6 mg/L). Blood culture was performed and empirical intravenous meropenem was commenced and labor was induced. After 24 h of incubation, blood culture yielded a Gram-positive bacillus, which was subsequently identified as L. monocytogenes. Meropenem was stopped and intravenous ampicillin was commenced. Examination of the cerebrospinal fluid revealed no abnormality. She became afebrile 2 days later and antibiotics were kept for a total of 15 days. Histopathological examination of the placenta showed severe acute chorioamnionitis involving the extraplacental membranes, acute villitis, intervillous abscess formation and retroplacental hematoma. L. monocytogenes was also isolated from the placental tissue.

The detailed clinical course of Case 5 has been reported elsewhere (40). Briefly, case 5 had a history of Talaromyces marneffei infection in March 2019 and was diagnosed to have anti-interferon gamma autoantibodies in May 2021. He was admitted in June 2021 because of acute onset of fever, severe headache and malaise. The total white cell count and neutrophils were elevated to 24.5 × 109/L and 21.2 × 109/L, respectively. Liver and renal function tests were mildly deranged. C-reactive protein was elevated at 282.4 mg/L. Blood culture was performed. Empirical intravenous piperacillin-tazobactam and voriconazole were commenced. A Gram-positive bacillus was isolated from blood culture after 21 h of incubation. The bacterium was subsequently identified as L. monocytogenes. Examination of the cerebrospinal fluid showed a cell count of 387 × 106/L, with 8% neutrophils, 10% lymphocytes and 82% monocytes, glucose of 2.8 mmol/L and protein of 373 mg/L. Bacterial culture was negative but next-generation sequencing revealed L. monocytogenes DNA. Piperacillin-tazobactam was stopped and intravenous ampicillin was commenced. Subsequently, the patient was also diagnosed to have disseminated Mycobacterium kansasii infection and was treated accordingly.

Discussion

During the last decade or so, there has been a marked increase in the success in the elucidation of the molecular mechanisms behind primary immunodeficiency syndromes that result in opportunistic infections. Some of these syndromes include anti-interferon gamma autoantibody (an immunological defect typically associated with infections caused by intracellular pathogens) and mutations in genes that encode key players of various cellular and immunological pathways (e.g., STAT3, TSC2) (41). In the same period of time, the surge in the use of targeted therapies, such as kinase inhibitors and antibodies against various targets in the cellular and immunological pathways, has led to secondary immunodeficiency; which in turn has resulted in opportunistic infections (2). In the present cohort, all the five cases with listeriosis in our hospital had predisposing factors, some of the well-known ones being pregnancy (case 3 and 4) and corticosteroid therapy (case 1, 2 and 3). On the other hand, it is of note that 60% of the cases had either the above-mentioned primary immunodeficiency syndrome (case 5) or secondary immunodeficiency induced by targeted therapy (case 1 and 2). In fact, the case of listeria bacteremic meningitis (case 5) was the first report of listeriosis in a patient with anti-interferon gamma autoantibody in the literature (40). For the two patients who had targeted therapy (case 1 and 2), both of them received inhibitors of the EGFR/HER2 pathway during their course of lung and breast cancer therapy, respectively. Gefitinib and osimertinib are EGFR tyrosine kinase inhibitors, lapatinib is a dual tyrosine kinase inhibitor on the EGFR/HER2 pathway, afatinib is a tyrosine kinase inhibitor that can bind to EGFR, HER2 and HER4, and trastuzumab is an anti-HER2 monoclonal antibody. Although it has been shown in various studies and meta-analysis that inhibitors of the EGFR/HER2 pathway were associated with higher risks and severity of infections (4244), the relative contribution of them is often difficult to quantify, as these patients are usually prescribed with other medications, such as corticosteroids, with immunosuppressive effects. In fact, both case 1 and 2 have also been given corticosteroid and chemotherapy for their underlying malignancies in addition to the EGFR/HER2 pathway inhibitors.

Targeted therapy is an important predisposing factor for listeriosis. The first patient reported to have listeria infection complicating targeted therapy was a patient with Crohn's disease on infliximab, an anti-TNFα monoclonal antibody (5). Since then, including the two cases in the present cohort, a total of 82 cases of listeriosis complicating targeted therapy have been reported in the scientific literature (537, 4557). For 69 out of the 82 patients, gender, age, and clinical information were reported (511, 1326, 2832, 3437, 4557). The most common underlying diseases in these patients were autoimmune diseases (Figure 1A), whereas the commonest targeted therapy used was anti-TNFα monoclonal antibody (Figure 1B). In fact, the only case of listeriosis associated with inhibitors of the EGFR/HER2 pathway in the literature was a patient with metastatic breast cancer who received trastuzumab and lapatinib (47). The two patients in the present cohort who received gefitinib/osimertinib/afatinib and trastuzumab/lapatinib, respectively represent the second and third cases of patients with listeria infections related to inhibitors of the EGFR/HER2 pathway. For the listeria infection, the majority had bacteremia (Figure 2), in line with the present cohort where all five patients were blood culture positive. Central nervous system infection, present in one of our patients, was also commonly observed (Figure 2). Interestingly, around 80% of the listeria cases complicating targeted therapy were reported from the western world (Figure 1C). We speculate that this is at least partially due to the dietary habits and culinary traditions in these countries. It is important to note, but many clinicians may not be aware of, that listeria bacteria are resistant to cephalosporins, therefore in suspected cases ampicillin or penicillin should be added. As shown in the present cohort, two out of the five patients with listeriosis were on targeted therapy, which made it an important risk factor to consider. Therefore, listeriosis is an important differential diagnosis in patients on targeted therapy who present with sepsis and/or central nervous system infection and the use of antibiotic regimens that cover listeria is crucial for empirical treatment. Furthermore, avoidance of high-risk food items in these patients is important for the prevention of listeriosis.

FIGURE 1
www.frontiersin.org

Figure 1. (A) Distribution of underlying diseases in patients on targeted therapy with listeriosis. (B) Distribution of the type of targeted therapy in these patients. (C) Distribution of these patients with listeriosis in different countries or regions.

FIGURE 2
www.frontiersin.org

Figure 2. Types of listeria infection in patients on targeted therapy.

The incidence of listeriosis could be underestimated. One of the most important causes of culture-negative infections is partially treated pyogenic bacterial infections. In the present cohort, although L. monocytogenes was isolated from the blood culture of case 5, it could not be recovered from the cerebrospinal fluid, despite the fact that there was increased white cell count and protein in the cerebrospinal fluid. Subsequently, the cerebrospinal fluid was sent for next-generation sequencing which confirmed the diagnosis of listeria meningitis. In 2020, we encountered a 26-year-old previously healthy woman who presented with recent onset of fever, severe headache and altered mental function. She had diarrhea for 4 days and has been treated with antibiotics. On admission, her temperature was 40.1°C. She also had neck rigidity, delirium and nystagmus. Examination of the cerebrospinal fluid revealed elevated white cell count with predominant neutrophils, increased protein and decreased glucose levels. Although Gram-smear revealed abundant Gram-positive rods, no bacteria could be isolated. All other microbiological investigations were negative. We speculate that this patient also had listeria meningoencephalitis, although it could not be confirmed microbiologically, as the patient had received antibiotics for a few days before lumbar puncture. She was treated as such accordingly and then recovered. These two cases illustrated that listeria infections could have been underestimated. A high index of suspicion is important and the use of next-generation sequencing would be useful for identifying more cases of partially treated listeriosis (40, 58).

Data Availability Statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

Ethics Statement

The studies involving human participants were reviewed and approved by the Institutional Review Board of The University of Hong Kong - Shenzhen Hospital. The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author Contributions

FX and PW conceptualized the study and wrote the manuscript. FX reviewed the clinical data. SKFL supervised the microbiological investigations. All authors have read and approved the final version of the manuscript.

Funding

This study was partly supported by Sanming Project of Medicine in Shenzhen, China (SZSM201911014) and the seed fund of The University of Hong Kong-Shenzhen Hospital (HKUSZH201901036). The funders had no role in study design, data collection or analysis, decision to publish, or preparation of the manuscript.

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.

Publisher's Note

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.

References

1. Keane J, Gershon S, Wise RP, Mirabile-Levens E, Kasznica J, Schwieterman WD, et al. Tuberculosis associated with infliximab, a tumor necrosis factor alpha-neutralizing agent. N Engl J Med. (2001) 345:1098–104. doi: 10.1056/NEJMoa011110

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Chan JF, Chan TS, Gill H, Lam FY, Trendell-Smith NJ, Sridhar S, et al. Disseminated infections with talaromyces marneffei in non-aids patients given monoclonal antibodies against CD20 and kinase inhibitors. Emerg Infect Dis. (2015) 21:1101–6. doi: 10.3201/eid2107.150138

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Choi K, Deval N, Vyas A, Moran C, Cha SS, Mertz LE, et al. The utility of screening for coccidioidomycosis in recipients of inhibitors of tumor necrosis factor α. Clin Infect Dis. (2019) 68:1024–30. doi: 10.1093/cid/ciy620

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Tsiodras S, Samonis G, Boumpas DT, Kontoyiannis DP. Fungal infections complicating tumor necrosis factor alpha blockade therapy. Mayo Clin Proc. (2008) 83:181–94.

PubMed Abstract | Google Scholar

5. Morelli J, Wilson FA. Does administration of infliximab increase susceptibility to listeriosis? Am J Gastroenterol. (2000) 95:841–2. doi: 10.1111/j.1572-0241.2000.01872.x

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Kamath BM, Mamula P, Baldassano RN, Markowitz JE. Listeria meningitis after treatment with infliximab. J Pediatr Gastroenterol Nutr. (2002) 34:410–2. doi: 10.1097/00005176-200204000-00018

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Glück T, Linde HJ, Schölmerich J, Müller-Ladner U, Fiehn C, Bohland P. Anti-tumor necrosis factor therapy and Listeria monocytogenes infection: report of two cases. Arthritis Rheum. (2002) 46:2255–7. doi: 10.1002/art.10374

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Slifman NR, Gershon SK, Lee JH, Edwards ET, Braun MM. Listeria monocytogenes infection as a complication of treatment with tumor necrosis factor alpha-neutralizing agents. Arthritis Rheum. (2003) 48:319–24. doi: 10.1002/art.10758

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Aparicio AG, Muñoz-Fernández S, Bonilla G, Miralles A, Cerdeño V, Martín-Mola E. Report of an additional case of anti-tumor necrosis factor therapy and Listeria monocytogenes infection: comment on the letter by Glück et al. Arthritis Rheum. (2003) 48:1764–6. doi: 10.1002/art.11019

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Tweezer-Zaks N, Shiloach E, Spivak A, Rapoport M, Novis B, Langevitz P. Listeria monocytogenes sepsis in patients treated with anti-tumor necrosis factor-alpha. Isr Med Assoc J. (2003) 5:829–30.

PubMed Abstract | Google Scholar

11. Bowie VL, Snella KA, Gopalachar AS, Bharadwaj P. Listeria meningitis associated with infliximab. Ann Pharmacother. (2004) 38:58–61. doi: 10.1345/aph.1D151

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Pagliano P, Attanasio V, Fusco U, Mohamed DA, Rossi M, Faella FS. Does etanercept monotherapy enhance the risk of Listeria monocytogenes meningitis? Ann Rheum Dis. (2004) 63:462–3. doi: 10.1136/ard.2003.015966

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Nadarajah K, Pritchard C. Listeria monocytogenes septic arthritis in a patient treated with etanercept for rheumatoid arthritis. J Clin Rheumatol. (2005) 11:120–2. doi: 10.1097/01.rhu.0000158551.39738.de

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Rachapalli S, O'Daunt S. Septic arthritis due to Listeria monocytogenes in a patient receiving etanercept. Arthritis Rheum. (2005) 52:987. doi: 10.1002/art.20876

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Schett G, Herak P, Graninger W, Smolen JS, Aringer M. Listeria-associated arthritis in a patient undergoing etanercept therapy: case report and review of the literature. J Clin Microbiol. (2005) 43:2537–41. doi: 10.1128/JCM.43.5.2537-2541.2005

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Williams G, Khan AA, Schweiger F. Listeria meningitis complicating infliximab treatment for Crohn's disease. Can J Infect Dis Med Microbiol. (2005) 16:289–92. doi: 10.1155/2005/814698

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Dixon WG, Watson K, Lunt M, Hyrich KL, Silman AJ, Symmons DP, et al. Rates of serious infection, including site-specific and bacterial intracellular infection, in rheumatoid arthritis patients receiving anti-tumor necrosis factor therapy: results from the British society for rheumatology biologics register. Arthritis Rheum. (2006) 54:2368–76. doi: 10.1002/art.21978

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Kesteman T, Yombi JC, Gigi J, Durez P. Listeria infections associated with infliximab: case reports. Clin Rheumatol. (2007) 26:2173–5. doi: 10.1007/s10067-007-0660-8

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Izbéki F, Nagy F, Szepes Z, Kiss I, Lonovics J, Molnár T. Severe Listeria meningoencephalitis in an infliximab-treated patient with Crohn's disease. Inflamm Bowel Dis. (2008) 14:429–31. doi: 10.1002/ibd.20286

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Peña-Sagredo JL, Hernández MV, Fernandez-Llanio N, Giménez-Ubeda E, Muñoz-Fernandez S, Ortiz A, et al. Listeria monocytogenes infection in patients with rheumatic diseases on TNF-alpha antagonist therapy: the Spanish study group experience. Clin Exp Rheumatol. (2008) 26:854–9.

PubMed Abstract | Google Scholar

21. Murphy G, Schmidt-Martin D, Hynes BG, Harney S. Systemic listeriosis with adalimumab therapy. J Clin Rheumatol. (2009) 15:369–70. doi: 10.1097/RHU.0b013e3181bf93cd

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Khatamzas E, Hughes H, Grant KA, McLauchlin J, Bowler IC. The increasing prevalence of listeriosis–what are we missing? QJM. (2010) 103:519–22. doi: 10.1093/qjmed/hcp181

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Katsanos KH, Kostapanos M, Zois CD, Vagias I, Tsianos EV. Listeria monocytogenes infection 2 days after infliximab initiation in a patient with ulcerative colitis. Annals Gastroenterol. (2010) 23:209–10.

Google Scholar

24. Ramos JM, García-Sepulcre MF, Masiá M, Brotons A, Grau MC, Gutiérrez F. Listeria monocytogenes infection in patients with inflammatory bowel diseases receiving anti-tumor necrosis factor therapy. Rev Esp Enferm Dig. (2010) 102:614–6. doi: 10.4321/s1130-01082010001000014

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Kelesidis T, Salhotra A, Fleisher J, Uslan DZ. Listeria endocarditis in a patient with psoriatic arthritis on infliximab: are biologic agents as treatment for inflammatory arthritis increasing the incidence of Listeria infections? J Infect. (2010) 60:386–96. doi: 10.1016/j.jinf.2010.02.009

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Chuang MH, Singh J, Ashouri N, Katz MH, Arrieta AC. Listeria meningitis after infliximab treatment of ulcerative colitis. J Pediatr Gastroenterol Nutr. (2010) 50:337–9. doi: 10.1097/MPG.0b013e3181a70f3a

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Lin TS, Donohue KA, Byrd JC, Lucas MS, Hoke EE, Bengtson EM, et al. Consolidation therapy with subcutaneous alemtuzumab after fludarabine and rituximab induction therapy for previously untreated chronic lymphocytic leukemia: final analysis of CALGB 10101. J Clin Oncol. (2010) 28:4500–6. doi: 10.1200/JCO.2010.29.7978

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Willson KJ, Jacob A, Shetti MP, Bhatia R, Yee K, Osler W. Listeria monocytogenes infection in Crohn's disease treated with adalimumab. Med J Aust. (2012) 197:466–7. doi: 10.5694/mja11.10521

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Abreu C, Magro F, Vilas-Boas F, Lopes S, Macedo G, Sarmento A. Listeria infection in patients on anti-TNF treatment: report of two cases and review of the literature. J Crohns Colitis. (2013) 7:175–82. doi: 10.1016/j.crohns.2012.04.018

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Mathews BK, Chuang C, Rawal A, Gertner E. Listeria rhomboencephalitis in a patient on a tumor necrosis factor α inhibitor (etanercept). J Clin Rheumatol. (2014) 20:325–7. doi: 10.1097/RHU.0000000000000151

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Miranda-Bautista J, Padilla-Suárez C, Bouza E, Muñoz P, Menchén L, Marín-Jiménez I. Listeria monocytogenes infection in inflammatory bowel disease patients: case series and review of the literature. Eur J Gastroenterol Hepatol. (2014) 26:1247–52. doi: 10.1097/MEG.0000000000000188

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Davies R, Dixon WG, Watson KD, Lunt M., BSRBR Control Centre Consortium, Symmons DP, et al. Influence of anti-TNF patient warning regarding avoidance of high risk foods on rates of listeria and salmonella infections in the UK. Ann Rheum Dis. (2013) 72:461–2. doi: 10.1136/annrheumdis-2012-202228

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Parihar V, Maguire S, Shahin A, Ahmed Z, O'Sullivan M, Kennedy M, et al. Listeria meningitis complicating a patient with ulcerative colitis on concomitant infliximab and hydrocortisone. Ir J Med Sci. (2016) 185:965–7. doi: 10.1007/s11845-015-1355-9

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Tsuchiya A, Terai S. Listeria Meningitis during Infliximab-based treatment for ulcerative colitis. Intern Med. (2018) 57:2603. doi: 10.2169/internalmedicine.0695-18

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Krijthe BP, Hermans MAW, Schurink CAM, van Daele PLA. Listeria infection in patients using anti-TNFα treatment: Should there be preventive strategies? Eur J Intern Med. (2019) 68:e15–6. doi: 10.1016/j.ejim.2019.07.027

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Horigome R, Sato H, Honma T, Terai S. Septicemic listeriosis during adalimumab- and golimumab-based treatment for ulcerative colitis: case presentation and literature review. Clin J Gastroenterol. (2020) 13:22–5. doi: 10.1007/s12328-019-01005-6

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Hung DLL, Lau SKP, Woo PCY. Severe sepsis caused by Listeria monocytogenes in a patient given monoclonal antibodies against CD38 and proteosome inhibitor. Infect Microb Dis. (2019) 1:30–31. doi: 10.1097/IM9.0000000000000003

CrossRef Full Text | Google Scholar

38. Carroll KC, Pfaller MA. Manual of Clinical Microbiology 12th edition. Washington DC: ASM Press (2019). 2832 p.

Google Scholar

39. Lau SK, Tang BS, Teng JL, Chan TM, Curreem SO, Fan RY, et al. Matrix-assisted laser desorption ionisation time-of-flight mass spectrometry for identification of clinically significant bacteria that are difficult to identify in clinical laboratories. J Clin Pathol. (2014) 67:361–6. doi: 10.1136/jclinpath-2013-201818

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Xing F, Hung DL, Lo SKF, Chen S, Lau SKP, Woo PCY. Next-generation sequencing-based diagnosis of bacteremic Listeria monocytogenes meningitis in a patient with anti-interferon gamma autoantibodies: a case report. Infect Microb Dis. (2022) 4:44–6. doi: 10.1097/IM9.0000000000000080

CrossRef Full Text | Google Scholar

41. Browne SK, Burbelo PD, Chetchotisakd P, Suputtamongkol Y, Kiertiburanakul S, Shaw PA, et al. Adult-onset immunodeficiency in Thailand and Taiwan. N Engl J Med. (2012) 367:725–34. doi: 10.1056/NEJMoa1111160

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Wang Y, Wang M, Wang Q, Geng Z, Sun M. Incidence and risk of infections associated with EGFR-TKIs in advanced non-small-cell lung cancer: a systematic review and meta-analysis of randomized controlled trials. Oncotarget. (2017) 8:29406–15. doi: 10.18632/oncotarget.14707

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Funakoshi T, Suzuki M, Muss HB. Infection risk in breast cancer patients treated with trastuzumab: a systematic review and meta-analysis. Breast Cancer Res Treat. (2015) 149:321–30. doi: 10.1007/s10549-014-3184-3

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Qi WX, Fu S, Zhang Q, Guo XM. Incidence and risk of severe infections associated with anti-epidermal growth factor receptor monoclonal antibodies in cancer patients: a systematic review and meta-analysis. BMC Med. (2014) 12:203. doi: 10.1186/s12916-014-0203-5

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Ng HJ, Lim LC. Fulminant hepatitis B virus reactivation with concomitant listeriosis after fludarabine and rituximab therapy: case report. Ann Hematol. (2001) 80:549–52. doi: 10.1007/s002770100346

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Barnadas M, Roe E, Brunet S, Garcia P, Bergua P, Pimentel L, et al. Therapy of paraneoplastic pemphigus with Rituximab: a case report and review of literature. J Eur Acad Dermatol Venereol. (2006) 20:69–74. doi: 10.1111/j.1468-3083.2005.01345.x

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Oliveira M, Braga S, Passos-Coelho JL, Fonseca R, Oliveira J. Complete response in HER2+ leptomeningeal carcinomatosis from breast cancer with intrathecal trastuzumab. Breast Cancer Res Treat. (2011) 127:841–4. doi: 10.1007/s10549-011-1417-2

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Sifuentes Giraldo WA, Guillén Astete CA, Amil Casas I, Gámir Gámir ML. Listeria monocytogenes meningoencephalitis during the treatment with rituximab and mycophenolate mofetil in a patient with pediatric-onset systemic lupus erythematosus. Reumatol Clin. (2015) 11:125–6. doi: 10.1016/j.reuma.2014.07.006

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Al-Harbi TM, Al-Muammar SA, Ellis RJ. Brain abscess following rituximab infusion in a patient with pemphigus vulgaris. Am J Case Rep. (2015) 16:65–68. doi: 10.12659/AJCR.892635

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Cellina M, Fetoni V, Baron P, Orsi M, Oliva G. Listeria meningoencephalitis in a patient with rheumatoid arthritis on anti-interleukin six receptor antibody tocilizumab. J Clin Rheumatol. (2015) 21:330. doi: 10.1097/RHU.0000000000000287

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Rau D, Lang M, Harth A, Naumann M, Weber F, Tumani H, et al. Listeria meningitis complicating alemtuzumab treatment in multiple sclerosis–report of two cases. Int J Mol Sci. (2015) 16:14669–6. doi: 10.3390/ijms160714669

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Onder ME, Gun H, Kimyon G, Zengin O, Onat AM, Kisacik B. Brain abscesses due to listeria monocytogenes after rituximab therapy. J Clin Rheumatol. (2016) 22:233–4. doi: 10.1097/RHU.0000000000000398

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Holmøy T, von der Lippe H, Leegaard TM. Listeria monocytogenes infection associated with alemtuzumab - - a case for better preventive strategies. BMC Neurol. (2017) 17:65. doi: 10.1186/s12883-017-0848-8

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Canham LJW, Manara A, Fawcett J, Rolinski M, Mortimer A, Inglis KEA, et al. Mortality from Listeria monocytogenes meningoencephalitis following escalation to alemtuzumab therapy for relapsing-remitting Multiple Sclerosis. Mult Scler Relat Disord. (2018) 24:38–41. doi: 10.1016/j.msard.2018.05.014

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Pappolla A, Midaglia L, Boix Rodríguez CP, et al. Simultaneous CMV and Listeria infection following alemtuzumab treatment for multiple sclerosis. Neurology. (2019) 92:296–8. doi: 10.1212/WNL.0000000000006801

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Mazzitelli M, Barone S, Greco G, Serapide F, Valentino P, Giancotti A, et al. Listeria infection after treatment with alemtuzumab: a case report and literature review. Would antibiotic prophylaxis be considered? Infez Med. (2020) 28:258–62.

PubMed Abstract | Google Scholar

57. Ueno T, Ohta T, Imanaga H, Nakazawa M, Sato Y, Sugio Y, et al. Listeria monocytogenes bacteremia during isatuximab therapy in a patient with multiple Myeloma. Intern Med. (2021) 60:3605–8. doi: 10.2169/internalmedicine.7509-21

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Yao M, Zhou J, Zhu Y, Zhang Y, Lv X, Sun R, et al. Detection of listeria monocytogenes in CSF from three patients with meningoencephalitis by next-generation sequencing. J Clin Neurol. (2016) 12:446–51. doi: 10.3988/jcn.2016.12.4.446

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Listeria monocytogenes, opportunistic infection, targeted therapy, EGFR, HER2

Citation: Xing F, Lo SKF, Lau SKP and Woo PCY (2022) Listeriosis in a Metropolitan Hospital: Is Targeted Therapy a Risk Factor for Infection? Front. Med. 9:888038. doi: 10.3389/fmed.2022.888038

Received: 02 March 2022; Accepted: 13 April 2022;
Published: 29 April 2022.

Edited by:

Giusto Trevisan, University of Trieste, Italy

Reviewed by:

Mau Ern Poh, University Malaya Medical Centre, Malaysia
Serena Bonin, University of Trieste, Italy

Copyright © 2022 Xing, Lo, Lau and Woo. 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: Patrick C. Y. Woo, cGN5d29vQGhrdS5oaw==

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.