Lu Qin
Lan-Fang Tang
Lei Cheng
Hui-Ying Wang- 1Department of Pulmonology, the Children’s Hospital of Zhejiang University School of Medicine, Hangzhou, China
- 2Department of Otorhinolaryngology & Clinical Allergy Center, The First Affiliated Hospital, Nanjing Medical University, Nanjing, China
- 3Department of Allergy and Clinical Immunology, the Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China
IgG4 is a subclass of IgG antibody with a unique molecular feature of (Fragment antigen- binding) Fab-arm exchange, allowing bispecific antigen binding in a mono-valent manner. With low binding affinity to C1q and Fcγreceptors, IgG4 is incapable of forming immune complexes and activating the complement pathway, exhibiting a non-inflammatory feature. IgG4 is produced similarly to IgE and is considered a modified reaction to IgE class-switching response under certain conditions. It could also counteract IgE-activated inflammation. However, the clinical significance of IgG4 in allergic diseases is complex and controversial. Three viewpoints have been suggested to describe the role of IgG4. IgG4 can act as a tolerance–inducer to play a protective role under repeated and rapid incremental dosing of allergen exposure in allergen immunotherapy (AIT), supported by allergies in cat raisers and venom desensitization in beekeepers. Another viewpoint accepted by mainstream specialists and guidelines of Food Allergy and Management in different countries points out that food-specific IgG4 is a bystander in food allergy and should not be used as a diagnostic tool in clinical work. However, eosinophilic esophagitis (EoE) investigation revealed a direct clinical relevance between physiopathology and serum IgG4 in cow milk and wheat. These factors indicate that allergen-specific IgG4 plays a multifaceted role in allergic diseases that is protective or pathogenic depending on different allergens or exposure conditions.
Introduction
Subclasses of IgG antibodies were discovered in the 1960s (1). IgG4 is one of the subclasses detected recently and constitutes about 5% of total IgG, the smallest portion among all IgGs in serum. Although these different subtypes of IgG have more than 90% identical amino acids, they display different immunological effects such as immune complex formation and complement activation. Previous studies have revealed that different IgG subclasses are associated with different antigens. IgG1and IgG2 subclass is usually associated with the response to bacterial polysaccharides. IgG3 is a potent pro-inflammatory antibody to induce effector function (2), while IgG4 is for non-microbial allergens.
IgG4 is conventionally considered non-inflammatory or anti-inflammatory because it cannot form large immune complexes and activate complement component pathways (3). Thus, its monoclonal antibodies are applied as therapeutics in tumors, rheumatic arthritis, and asthma (4–10). However, IgG4 is also associated with various diseases, including IgG4-related diseases, autoimmune and hematologic disorders, parasitic infections, and neoplasms (11, 12). A recent study showed that serum IgG4 levels could predict COVID-19 related-mortality (13). These studies indicate that IgG4 is also pathogenic and can induce Th2 inflammation following final fibrosis.
The clinical significance of IgG4 in allergic diseases is controversial. The earliest recognition of IgG4 in allergies was from Allergen-specific immunotherapy (AIT) data, demonstrating a tolerance-inducing function (14–16). However, later clinical observations revealed that allergen-specific IgG4 was associated with allergic sensitization and correlated to allergic diseases, such as allergic rhinitis (AR), asthma, atopic dermatitis (AD), and anaphylaxis (17–23). IgG4 levels may vary significantly in healthy individuals (24), strongly hindering its clinical application as a diagnostic tool. Nevertheless, recent findings from molecular structure and clinical investigations have brought new insights into this subset of IgG antibodies in allergic diseases.
The present study provides a comprehensive review of recent studies on IgG4, its structure features, immune biology, interaction with IgE, and different roles in different allergic statuses.
Unique molecular feature of Fab-arm exchange and impact on its immune response
IgG4 has a unique molecular feature distinguished from other subclasses of IgGs, which results in diversity in the immune response. Like other subclasses of IgG, the basic molecular structure of IgG4 is composed of two light chains (-25 kD) and two heavy chains (-50 kD) paired together (Figure 1A) (25, 26). The light chain has one constant domain (CL) and one variable domain (VL), while the heavy chain consists of 3 IgG4-specific constant domains (CH, including CH1, CH2, and CH3) and one variable domain (VH). The variable domains of the heavy (VH) and light chain (VL), with the attached CL and CH1 domains, respectively, formed the ‘fragment antigen-binding region’ (Fab-region), which is highly specific for one epitope. However, unlike other subclasses of IgG composed of two same chains, IgG4 are dynamic molecules that dissociate into two half molecules with one light chain and one heavy chain, then reassemble with another half one. It is called FAE and results in a bi-specific binding antibody (Figure 1B) (27, 28). The phenomenon is due to the serine replacing proline in the hinge region at positions 288 and 331 (29, 30), which makes the disulfide bond unstable. The half-molecular form of IgG4 exists up to 10% in circulation, and the main body is full-molecular IgG4 with bispecific epitopes (31). The pathogenesis and the regulating factors of FAE are still unclear. The exchange could occur in vivo or in vitro under some conditions or spontaneously (28).
Figure 1 Structure of IgG4 antibody and Fab-arm exchange. (A) Inter- and intra-chain disulfide bonds give structure to IgG4. (B) Antibodies separate into ‘half-molecules’, each comprising one heavy and one light chain. Half-molecules recombine to form bi-specific antibodies.
This unique feature of the bi-specificity of IgG4 enables it to combine two different allergens via one molecule (3, 28) and behave as a mono-valent antibody. AIT using different antigens showed the best demonstration of this (25). In vitro experiments have also exhibited that IgG4 is incapable of forming complexes via immuno-precipitation (28, 32). Therefore, the complement cascade cannot activate to cause cell lysis and the classical pathway.
The site of P331 is the binding site to C1q, and the amino acid mutation caused the low affinity of IgG4 to C1q and the consequent tendency to interact with other immunoglobulins (33). Thus, IgG4 can prevent the biological effect of the complement IgG1 subclass. Moreover, IgG4 has no affinity to the receptors FcgRIIIa and FcgRIIIb (34, 35). These features render IgG4 an anti-inflammatory or tolerance-genic antibody.
It was noted that FAE produces 2 types of IgG4 since recombination is a random process. One has bi-specific epitopes composed of 2 arms with different allergen sources. Another one might have 2 arms with a similar allergen source, meaning it might behave in a bivalent manner and be pathogenic in some inflammatory diseases, such as allergic diseases.
IgG4 synthesis and its interaction with IgE
The production of IgG4 seems to have a very similar pathway to IgE. Both are part of the Th2 immune response, triggered by allergen exposure and produced by a class switch on B cells dependent on IL-4/IL-13. Th2 cytokines (e.g., IL-5, IL-6, IL-9, and IL-13) that involve IgE production have similar effects on IgG4 production. However, what predominates the diverging to IgE or IgG4 is still unclear. It was speculated that the allergen stimulus might be the most important factor in initiating the switch to IgE or IgG4. Antibody response to natural cat allergen exposure provides a clear picture, with high IgG4 and low IgE responses in cat raisers. AIT further exhibits a dynamic switch of IgE production to IgG4 production after repeated and rapid increments of allergen exposure. Relevant studies found that IL-10 played a critical role in this shift of IgE to IgG4. In vitro experiments showed a culture of peripheral blood monocytes with the addition of IL-10 could achieve IgG4 production over IgE, and IL-10-producing T regulatory cells suppressed IgE production (36, 37). The IgG4 production after AIT is correlated to the significant elevation of serum IL-10. IL-21, a pleiotropic cytokine, is also recently found to have a role in shifting IgE response to IgG4 response (38). Thereby, a modified Th2 response was nominated to describe this phenomenon (39), which helps illustrate the clinical significance of IgG4, as discussed later.
The immune biological role of IgG4 appears to counteract IgE through different pathways. First, IgG4 can block IgE binding to specific allergens in serum through competition, though the difference in repertoires may influence the results (40, 41). Studies of food allergens showed that IgE and IgG4 had similar binding patterns in peanut, milk, egg, and lentil allergy (42–45). Moreover, serum IgG4 responses to AIT were well documented as blocking allergen binding to receptor-bound IgE on antigen-presenting and effector cells (46, 47). The second and more critical pathway is the direct inhibition of IgE-mediated mast cell activation (Figure 2). IgE binds to the high-affinity receptor FcϵRI and triggers the degranulation reaction of mast cells. In contrast, IgG4 binds to the inhibitory receptor FcγRIIb to inhibit the above effects at both the initiation and effector phases of allergic immune responses (48–50). A grass pollen-specific IgG4 antibody isolated from a patient undertaking AIT blocked the interaction between allergen and IgE and inhibited basophil activation. In addition, it inhibited the IgE-facilitated antigen presentation by B cells which promotes allergic inflammation and the engagement of membrane CD23 by IgE-allergen complexes (46). Furthermore, the unique capacity of IgG4 for FAE, which means dissociation and re-pairing of IgG4 Fab arms, creates bispecific antibodies capable of interfering with IgE-allergen complex formation (28, 51). This interaction with IgE may contribute to the harmless or protective appearance of IgG4 in allergic diseases, but the clinical implication is likely much more complex.
Figure 2 The role of allergen-specific IgG4 in allergen exposure. (A) Acute allergen exposure may lead to IgE-mediated histamine-induced hypersensitivity reactions by high-affinity receptor FcϵRI. (B) Chronic allergen exposure may induce IgG4 formation and allergen binding by IgG4, thereby binds to the inhibitory receptor FcγRIIb which prevents hypersensitivity reactions and induces allergen tolerance.
Development of IgG4 and its association with allergic diseases
IgG4 could be detected in the serum of healthy subjects with a variance of a wide range. Multiple birth cohort studies have discovered the expression of IgG4 in the serum of infancy at a low level, rising to a peak at 2-3 years of age and declining after that (20, 52–55). However, higher levels or the ratio to total IgG of allergen-specific IgG4 have been associated with atopy in children. Despite the decline of the total IgG and IgG4 in egg and milk, the ratio of IgG4 to total IgG goes up from 15% at six months to 50% at 5 years in children with one parent of atopy (56). In children sensitized to foods, specific IgG4 peaks earlier and persists for 8 years and longer (20). Furthermore, maternal atopy is linked to IgG subclass antibodies to food and inhalant allergens in cord blood (52).. The studies showed that the maternal food-specific IgG4 antibody titer was related to allergy in children with AD (53). These data indicated that IgG of all subclasses, especially IgG4, is elevated earlier in children of atopic mothers, and the atopy in children is associated with elevated maternal IgG4 antibodies. However, the IgG4 response to different allergens is varied. IgG4 for food allergens was higher than inhalant allergens (e.g., pollen) (57). Among the food allergens, the level of IgG4 in cow’s milk was dramatically higher than in peanuts (58).
This association between IgG4 and allergy brings vital interest in its clinical significance, which is complex and controversial. Accumulated data from clinical observations demonstrate three viewpoints on the correlations of IgG4 in different statuses (Table 1). The first viewpoint is that IgG4 is protective and tolerogenic. Another perspective is that IgG4 has no value in clinical diagnosis and therapy as a bystander. However, recent studies found that IgG4 may play a pathogenic role in many allergic diseases, including respiratory, skin, and food allergies, as discussed in more detail below.
Table 1 Three viewpoints of clinical correlation of IgG4 in allergic diseases.
The protective role of IgG4 in allergic diseases
Anti-inflammation and tolerance-inducing in allergic diseases are the most common recognitions of IgG4, mainly based on its IgE-counteracting effector role and clinical observation of AIT. Just after the discovery of IgG4 in the early 1970s, three independent groups reported a significant increase in IgG4 levels after AIT (59, 60). In the following four decades, more data on AIT has accumulated a convincing body of evidence for the recognition of IgG4 as a biomarker of the tolerance inducer in AIT (61). These clinical investigations of AIT demonstrated a comprehensive overview of IgG4’s protective function in different types of allergens, including food allergens such as milk and eggs (62–65), inhalant allergens such as pollen or mite extracts (14), as well as venom proteins (66). These AIT studies demonstrated modified Th2 response under high concentrations of allergen exposure.
Anecdotal stories from people who raise cats as well as those of beekeepers also strongly support evidence of immune response to natural exposure. Hesselmar et al. reported a reduced risk of cat allergy in cat raisers (67), confirmed by Platts-Mills and Renand (39, 68). Plattes-Mills et al. further comprehensively studied the exposure concentration-related response of IgG4 with low sensitization of cat allergens. Beekeepers have demonstrated occupational exposure and natural desensitization with increased specific IgG4 (69), similar to tolerant animal laboratory workers chronically exposed to rodent allergens (70, 71).
In addition, the primary references of IgG4 showed that the appearance of IgG4 antibodies is usually associated with a decrease in symptoms. In a study on the mechanism of milk allergy and tolerance, it was reported that atopic individuals with milk protein tolerance were accompanied by increased food-specific IgG4 antibodies and a decrease in corresponding IgE (14). Children sensitized with aero-allergen-specific IgE antibodies also reported having no symptoms under a higher IgG/IgE ratio in sera, which inhibits the activation of basophils sensitized with aero-allergen IgE (15). Santos and colleagues found that higher levels of peanut-specific IgG4 correlate with tolerance in those subjects with positive specific IgE (16).
No value in the diagnosis and management of the allergic disease
Most specialists do not accept the clinical value of food allergen-specific IgG4 in food allergy, and its clinical application is vehemently opposed. Almost all guidelines on food allergy outline a negative opinion. A position paper by the EAACI task force from 2008 declared that food-specific IgG4 was not recommended as a diagnostic tool for food allergy (72). The American Academy of Allergy and Immunology Position Statement (AAAI) also holds the same opinion and concluded that using specific and nonspecific IgG4 does not serve as diagnostic and prognostic tests for clinical allergy (73). Therefore, the serological tests for food-specific IgG4 are disputable and seem to not be an indicative diagnostic tool for food allergy.
Studies have revealed the irrelevance of food-specific IgG4 to clinical symptoms of food allergy (74). The testing of food-specific IgG4 failed to distinguish double-blind placebo-controlled food challenge (DBPCFC)-positive from negative patients (75, 76). After eliminating IgG-positive foods, the success rates of hypersensitivity reactions like asthma, headache, fatigue, and serous otitis correspond to the high placebo effect of each manipulation in the diet (77). Lichtenstein et al. (78) also showed that IgG-specific mAb were binding to IgG-IgE complexes attached to basophil through IgE bound to the IgE receptor, which showed passive sensitization to anti-IgG could be blocked by previous exposure of the basophils to IgE. These cells cross-link the IgE receptors through the above complexes, which supports the idea that food-specific IgG4 antibody responses do not help assess allergic disease or plan food-elimination diets. A follow-up study on 2-5 year old of children with food allergies demonstrated that the occurrence of serum IgE and IgG antibodies to some food was parallel in most cases (79). Another study reported that none of the patients with positive food-specific IgG4 showed adverse reactions, neither immediate nor delayed, which means food-specific IgG4 does not indicate a food allergy or intolerance (80). High IgA, IgG1, or IgG4 in atopic children was not always consistent with allergic sensitization and atopic diseases (17, 18). Moreover, Calkhoven PG et al. (81) and Eysink PE et al. (82) both describe that food-specific IgG4 is commonly found in children without any clinical manifestation of allergy-like diseases. The outcome of those studies queries the usefulness of testing for food-specific IgG4 and even objects to it as a diagnostic tool in allergic disorders. The main explanation for this bystander effect is that food-specific IgG4 is a natural product of antigen exposure as part of the normal immune response to foods. Increasing evidence disagrees with this viewpoint.
Pathogenic role of IgG4 in allergic diseases
With the development of techniques in measurement and structural investigations, new features of pathogenic roles of IgG4 in allergic diseases are gradually recognized. Allergies are chronic inflammatory disorders involving various immune cells such as mast cells, eosinophils, and T lymphocytes (83). IgG4 was also found to be higher in patients with AR, asthma, and AD than in non-allergic subjects and had a positive correlation to allergic diseases (23). Elevation of serum IgG4 has additionally been seen in patients with aspirin-exacerbated respiratory disease (AERD), nasal polyposis, eosinophilia, and celiac diseases (84). Oka et al. conducted a series of studies of clinical investigations and revealed that serum IgG4 level is associated with the severity of chronic rhinosinusitis eosinophilic (CRS), and it could be a novel biomarker to predict post-operation reoccurrence (85, 86). The latest study using microarray immunoassay to assay the binding of IgG4 to lenti1 epitopes found that the signal intensities of positive epitopes were significantly greater in reactive patients than tolerant ones (45). Several studies confirmed that food-specific IgG4 served as an anaphylactic antibody against some foods and inhaled allergens in asthma and other atopic diseases (22, 87, 88). Further research has also demonstrated that some relevant allergic symptoms finally improved or disappeared when foods with positive IgG4 test results were avoided (89, 90).
The most solid evidence of IgG4’s pathogenicity in allergy are studies of Eosinophilic esophagitis (EoE) conducted by the Platts-Mills TAE group in children (91) and Clayton’s group in adults (92). EoE is a chronic Th2 cell-mediated disease of the esophagus that contributes to poor quality of life, dysphagia, and food impactions in all ages, characterized by esophageal dysfunction, and a productive eosinophil inflammation of the esophageal mucosa (91–95). It was first recognized as a form of food allergy by Kelly et al. (96) in 1995 and is now expected as the third form of food allergy suggested by Platts-Mills TAE in Virginia (91). EoE has been well demonstrated as the adaptive Th2-type response to food antigens, with several characteristic cytokines and chemokines in food-specific responses (97–99). In 2014, Clayton et al. (92) reported that high serum IgG4 reacted with milk, wheat, egg, and nuts in adult EOE patients and, more critically. Biopsy specimens demonstrated the deposition of IgG4 in esophageal tissues, which indicated that, in adults, EoE is associated with food-specific IgG4 antibodies. A later case-control study of 20 adult EoE subjects and 10 non-EoE controls was performed and verified this association (100). In addition, another research also confirmed that food-specific IgG4 antibodies are easily collected along the esophageal lumen of EoE patients (101).
The results of serum IgG4 antibodies on EoE pediatric cases were also intriguing. Thomas’ group found both a high prevalence and very high titers of IgG4 antibodies to the cow’s milk proteins alpha-lactalbumin (Bos d 4), beta-lactoglobulin (Bos d 5), and casein (Bos d 8) as well as to gluten from wheat (102). The most persuasive evidence comes from the food avoidance and re-induce test. The symptoms and histopathology of IgG4 deposition disappeared completely after simple avoidance of cow milk and reoccurred after the food was re-introduced. Moreover, successful OIT for food allergies to peanuts, milk, or egg can cause an EoE-like condition with the elevation of food-specific IgG4 antibodies in serum (103). A different group from San Paulo, Brazil, presented the same findings at the American Academy of Allergy, Asthma, and Immunology (AAAAI) meeting in 2019 (104).
The underlying mechanism is still unclear. Factors such as food particles, and the undiscovered pathway of IgG4 to form an immune complex and activate mast cells, might be possible reasons (105, 106).
Conclusion
IgG4 has multiple profiles in allergic diseases due to its unique molecular feature and consequent biology. The FAE results in a dynamic antibody with bi-specific binding capability in a monovalent manner. A similar condition of IgG4 production to IgE induces the switch of IgE/IgG4. IgG4 plays different roles under different clinical conditions. It works as a tolerance inducer in AIT, cat raisers, and beekeepers, a bystander in food allergy, and a pathogenic role in EOE. The underlying mechanism of these multiple faces of IgG4 in allergic diseases is still unclear and needs further investigation. However, it brings new light to the treatment of allergic diseases as a therapeutical target. For EOE, avoidance of food with positive IgG4 is a good strategy to relieve the symptoms. For some allergies, the application of allergen-specific IgG4 antibodies might be an effective approach to creating a blockade.
Author contributions
LQ drafted the molecular feature, impact, and pathogenic role of the IgG4 section. H-YW drafted all remaining sections. All coauthors reviewed and edited the final manuscript. All authors contributed to the article and approved the submitted version.
Funding
This study was supported by the National Natural Science Foundation of China (81170016, 81470214 & 82070028), the Zhejiang Provincial Program for the Cultivation of High-Level Innovative Health Talents (2016), and the Innovation Team for the Diagnosis and Treatment of Childhood Asthma.
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
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References
2. Vidarsson G, Dekkers G, Rispens T. IgG subclasses and allotypes: from structure to effector functions. Front Immunol (2014) 5:520. doi: 10.3389/fimmu.2014.00520
3. Trampert DC, Hubers LM, van de Graaf SFJ, Beuers U. On the role of IgG4 in inflammatory conditions: lessons for IgG4-related disease. Biochim Biophys Acta Mol Basis Dis (2018) 1864(4 Pt B):1401–9. doi: 10.1016/j.bbadis.2017.07.038
4. Lefranc MP, Giudicelli V, Ginestoux C, Jabado-Michaloud J, Folch G, Bellahcene F, et al. IMGT, the international ImMunoGeneTics information system. Nucleic Acids Res (2009) 37(Database issue):D1006–12. doi: 10.1093/nar/gkn838
5. Feldmann M, Charles P, Taylor P, Maini RN. Biological insights from clinical trials with anti-TNF therapy. Springer Semin Immunopathol (1998) 20(1-2):211–28. doi: 10.1007/BF00832008
6. Miller DH, Khan OA, Sheremata WA, Blumhardt LD, Rice GP, Libonati MA, et al. A controlled trial of natalizumab for relapsing multiple sclerosis. N Engl J Med (2003) 348(1):15–23. doi: 10.1056/NEJMoa020696
7. Chan AC, Carter PJ. Therapeutic antibodies for autoimmunity and inflammation. Nat Rev Immunol (2010) 10(5):301–16. doi: 10.1038/nri2761
8. von Mehren M, Britten CD, Pieslor P, Saville W, Vassos A, Harris S, et al. A phase 1, open-label, dose-escalation study of BIIB022 (anti-IGF-1R monoclonal antibody) in subjects with relapsed or refractory solid tumors. Invest New Drugs (2014) 32(3):518–25. doi: 10.1007/s10637-014-0064-y
9. Newman R, Hariharan K, Reff M, Anderson DR, Braslawsky G, Santoro D, et al. Modification of the fc region of a primatized IgG antibody to human CD4 retains its ability to modulate CD4 receptors but does not deplete CD4(+) T cells in chimpanzees. Clin Immunol (2001) 98(2):164–74. doi: 10.1006/clim.2000.4975
10. Labrijn AF, Buijsse AO, van den Bremer ET, Verwilligen AY, Bleeker WK, Thorpe SJ, et al. Therapeutic IgG4 antibodies engage in fab-arm exchange with endogenous human IgG4. In vivo Nat Biotechnol (2009) 27(8):767–71. doi: 10.1038/nbt.1553
11. Turner JD, Faulkner H, Kamgno J, Kennedy MW, Behnke J, Boussinesq M, et al. Allergen-specific IgE and IgG4 are markers of resistance and susceptibility in a human intestinal nematode infection. Microbes Infect (2005) 7(7-8):990–6. doi: 10.1016/j.micinf.2005.03.036
12. Tang H, Yang H, Zhang P, Wu D, Zhang S, Zhao J, et al. Malignancy and IgG4-related disease: the incidence, related factors and prognosis from a prospective cohort study in China. Sci Rep (2020) 10(1):4910. doi: 10.1038/s41598-020-61585-z
13. Della-Torre E, Lanzillotta M, Strollo M, Ramirez GA, Dagna L, Tresoldi M, et al. Serum IgG4 level predicts COVID-19 related mortality. Eur J Intern Med (2021) 93:107–9. doi: 10.1016/j.ejim.2021.09.012
14. Ruiter B, Knol EF, van Neerven RJ, Garssen J, Bruijnzeel-Koomen CA, Knulst AC, et al. Maintenance of tolerance to cow's milk in atopic individuals is characterized by high levels of specific immunoglobulin G4. Clin Exp Allergy (2007) 37(7):1103–10. doi: 10.1111/j.1365-2222.2007.02749.x
15. Custovic A, Soderstrom L, Ahlstedt S, Sly PD, Simpson A, Holt PG. Allergen-specific IgG antibody levels modify the relationship between allergen-specific IgE and wheezing in childhood. J Allergy Clin Immunol (2011) 127(6):1480–5. doi: 10.1016/j.jaci.2011.03.014
16. Santos AF, James LK, Bahnson HT, Shamji MH, Couto-Francisco NC, Islam S, et al. IgG4 inhibits peanut-induced basophil and mast cell activation in peanut-tolerant children sensitized to peanut major allergens. J Allergy Clin Immunol (2015) 135(5):1249–56. doi: 10.1016/j.jaci.2015.01.012
17. Germano P, Pezzini A, Boccagni P, Zanoni G, Tridente G. Specific humoral response to cows' milk proteins and ovalbumin in children with atopic dermatitis. Int J Clin Lab Res (1993) 23(4):206–11. doi: 10.1007/BF02592310
18. Jenmalm MC, Björkstén B. Exposure to cow's milk during the first 3 months of life is associated with increased levels of IgG subclass antibodies to beta-lactoglobulin to 8 years. J Allergy Clin Immunol (1998) 102(4 Pt 1):671–8. doi: 10.1016/s0091-6749(98)70286-6
19. Batard T, Basuyaux B, Lambin P, Brémard-Oury C, Hamilton RG, David B, et al. Isotypic analysis of grass pollen-specific immunoglobulins in human plasma. 1. specialization of certain classes and subclasses in the immune response. Int Arch Allergy Immunol (1993) 100(1):68–78. doi: 10.1159/000236390
20. Scott-Taylor TH, O'B Hourihane J, Strobel S. Correlation of allergen-specific IgG subclass antibodies and T lymphocyte cytokine responses in children with multiple food allergies. Pediatr Allergy Immunol (2010) 21(6):935–44. doi: 10.1111/j.1399-3038.2010.01025.x
21. Vance GH, Thornton CA, Bryant TN, Warner JA, Warner JO. Ovalbumin-specific immunoglobulin G and subclass responses through the first 5 years of life in relation to duration of egg sensitization and the development of asthma. Clin Exp Allergy (2004) 34(10):1542–9. doi: 10.1111/j.1365-2222.2004.02058.x
22. Gwynn CM, Ingram J, Almousawi T, Stanworth DR. Bronchial provocation tests in atopic patients with allergen-specific IgG4 antibodies. Lancet (1982) 1(8266):254–6. doi: 10.1016/s0140-6736(82)90978-3
23. Liu PJ, Liu KL, Liao EC. Specific immunoglobulin G4 and immunoglobulin e titers to common food antigens in sera of children with allergic rhinitis. Altern Ther Health Med (2018) 24(6):38–45.
24. Nirula A, Glaser SM, Kalled SL, Taylor FR. What is IgG4? a review of the biology of a unique immunoglobulin subtype. Curr Opin Rheumatol (2011) 23(1):119–24. doi: 10.1097/BOR.0b013e3283412fd4
25. Schuurman J, Perdok GJ, Gorter AD, Aalberse RC. The inter-heavy chain disulfide bonds of IgG4 are in equilibrium with intra-chain disulfide bonds. Mol Immunol (2001) 38(1):1–8. doi: 10.1016/s0161-5890(01)00050-5
26. Angal S, King DJ, Bodmer MW, Turner A, Lawson AD, Roberts G, et al. A single amino acid substitution abolishes the heterogeneity of chimeric mouse/human (IgG4) antibody. Mol Immunol (1993) 30(1):105–8. doi: 10.1016/0161-5890(93)90432-b
27. Labrijn AF, Rispens T, Meesters J, Rose RJ, den Bleker TH, Loverix S, et al. Species-specific determinants in the IgG CH3 domain enable fab-arm exchange by affecting the noncovalent CH3-CH3 interaction strength. J Immunol (2011) 187(6):3238–46. doi: 10.4049/jimmunol.1003336
28. van der Neut Kolfschoten M, Schuurman J, Losen M, Bleeker WK, Martínez-Martínez P, Vermeulen E, et al. Anti-inflammatory activity of human IgG4 antibodies by dynamic fab arm exchange. Science (2007) 317(5844):1554–7. doi: 10.1126/science.1144603
29. Koneczny I. A new classification system for IgG4 autoantibodies. Front Immunol (2018) 9:97. doi: 10.3389/fimmu.2018.00097
30. King DJ, Adair JR, Angal S, Low DC, Proudfoot KA, Lloyd JC, et al. Expression, purification and characterization of a mouse-human chimeric antibody and chimeric fab' fragment. Biochem J (1992) 281(Pt 2):317–23. doi: 10.1042/bj2810317
31. Grey HM, Kunkel HG. H chain subgroups of myeloma proteins and normal 7S gamma-globulin. J Exp Med (1964) 120(2):253–66. doi: 10.1084/jem.120.2.253
32. Schuurman J, Perdok GJ, Mueller GA, Benjamin DC, Yong Tan K, Chapman MD, et al. Mouse/human chimeric IgG1 and IgG4 antibodies directed to the house dust mite allergen der p 2: use in quantification of allergen specific IgG. Clin Exp Allergy (1997) 27(9):1095–102. doi: 10.1111/j.1365-2222.1997.tb01262.x
33. Tao MH, Smith RI, Morrison SL. Structural features of human immunoglobulin G that determine isotype-specific differences in complement activation. J Exp Med (1993) 178(2):661–7. doi: 10.1084/jem.178.2.661
34. Nimmerjahn F, Ravetch JV. Fcgamma receptors as regulators of immune responses. Nat Rev Immunol (2008) 8(1):34–47. doi: 10.1038/nri2206
35. Ben Mkaddem S, Benhamou M, Monteiro RC. Understanding fc receptor involvement in inflammatory diseases: From mechanisms to new therapeutic tools. Front Immunol (2019) 10:811. doi: 10.3389/fimmu.2019.00811
36. Jeannin P, Lecoanet S, Delneste Y, Gauchat JF, Bonnefoy JY. IgE versus IgG4 production can be differentially regulated by IL-10. J Immunol (1998) 160(7):3555–61.
37. Robinson DS, Larché M, Durham SR. Tregs and allergic disease. J Clin Invest (2004) 114(10):1389–97. doi: 10.1172/JCI23595
38. Wood N, Bourque K, Donaldson DD, Collins M, Vercelli D, Goldman SJ, et al. IL-21 effects on human IgE production in response to IL-4 or IL-13. Cell Immunol (2004) 231(1-2):133–45. doi: 10.1016/j.cellimm.2005.01.001
39. Platts-Mills T, Vaughan J, Squillace S, Woodfolk J, Sporik R. Sensitisation, asthma, and a modified Th2 response in children exposed to cat allergen: a population-based cross-sectional study. Lancet (2001) 357(9258):752–6. doi: 10.1016/S0140-6736(00)04168-4
40. Aalberse RC, Dieges PH, Knul-Bretlova V, Vooren P, Aalbers M, van Leeuwen J. IgG4 as a blocking antibody. Clin Rev Allergy (1983) 1(2):289–302. doi: 10.1007/BF02991163
41. Van Milligen FJ, Craig S, Rogers BL, Van Swieten P, Aalberse RC. Differences between specificities of IgE and IgG4 antibodies: studies using recombinant chain 1 and chain 2 of the major cat allergen felis domesticus (Fel d) I. Clin Exp Allergy (1995) 25(3):247–51. doi: 10.1111/j.1365-2222.1995.tb01036.x
42. Martínez-Botas J, Cerecedo I, Zamora J, Vlaicu C, Dieguez MC, Gómez-Coronado D, et al. Mapping of the IgE and IgG4 sequential epitopes of ovomucoid with a peptide microarray immunoassay. Int Arch Allergy Immunol (2013) 161(1):11–20. doi: 10.1159/000343040
43. Sackesen C, Suárez-Fariñas M, Silva R, Lin J, Schmidt S, Getts R, et al. A new luminex-based peptide assay to identify reactivity to baked, fermented, and whole milk. Allergy (2019) 74(2):327–36. doi: 10.1111/all.13581
44. Shreffler WG, Lencer DA, Bardina L, Sampson HA. IgE and IgG4 epitope mapping by microarray immunoassay reveals the diversity of immune response to the peanut allergen, ara h 2. J Allergy Clin Immunol (2005) 116(4):893–9. doi: 10.1016/j.jaci.2005.06.033
45. Sackesen C, Erman B, Gimenez G, Grishina G, Yilmaz O, Yavuz ST, et al. IgE and IgG4 binding to lentil epitopes in children with red and green lentil allergy. Pediatr Allergy Immunol (2020) 31(2):158–66. doi: 10.1111/pai.13136
46. James LK, Shamji MH, Walker SM, Wilson DR, Wachholz PA, Francis JN, et al. Long-term tolerance after allergen immunotherapy is accompanied by selective persistence of blocking antibodies. J Allergy Clin Immunol (2011) 127(2):509–16.e5165. doi: 10.1016/j.jaci.2010.12.1080
47. Wilcock LK, Francis JN, Durham SR. IgE-facilitated antigen presentation: role in allergy and the influence of allergen immunotherapy. Immunol Allergy Clin North Am (2006) 26(2):333–ix. doi: 10.1016/j.iac.2006.02.004
48. Daëron M, Malbec O, Latour S, Arock M, Fridman WH. Regulation of high-affinity IgE receptor-mediated mast cell activation by murine low-affinity IgG receptors. J Clin Invest (1995) 95(2):577–85. doi: 10.1172/JCI117701
49. Strait RT, Morris SC, Finkelman FD. IgG-blocking antibodies inhibit IgE-mediated anaphylaxis in vivo through both antigen interception and fc gamma RIIb cross-linking. J Clin Invest (2006) 116(3):833–41. doi: 10.1172/JCI25575
50. Burton OT, Logsdon SL, Zhou JS, Medina-Tamayo J, Abdel-Gadir A, Noval Rivas M, et al. Oral immunotherapy induces IgG antibodies that act through FcγRIIb to suppress IgE-mediated hypersensitivity. J Allergy Clin Immunol (2014) 134(6):1310–7.e6. doi: 10.1016/j.jaci.2014.05.042
51. Collins AM, Davies JM. Enhanced cell-binding by allergen multimers: how complex is it? Immunol Cell Biol (2013) 91(2):115–7. doi: 10.1038/icb.2013.5
52. Jenmalm MC, Björkstén B. Cord blood levels of immunoglobulin G subclass antibodies to food and inhalant allergens in relation to maternal atopy and the development of atopic disease during the first 8 years of life. Clin Exp Allergy (2000) 30(1):34–40. doi: 10.1046/j.1365-2222.2000.00771.x
53. de Martino M, Rossi ME, Novembre E, Vierucci A. Occurrence and subclass distribution of IgG antibodies to dietary antigens in children with atopic dermatitis and in their mothers. Ann Allergy (1988) 61(4):253–8.
54. Duchén K, Einarsson R, Grodzinsky E, Hattevig G, Björkstén B. Development of IgG1 and IgG4 antibodies against beta-lactoglobulin and ovalbumin in healthy and atopic children. Ann Allergy Asthma Immunol (1997) 78(4):363–8. doi: 10.1016/S1081-1206(10)63197-3
55. Zar S, Benson MJ, Kumar D. Food-specific serum IgG4 and IgE titers to common food antigens in irritable bowel syndrome. Am J Gastroenterol (2005) 100(7):1550–7. doi: 10.1111/j.1572-0241.2005.41348.x
56. Rowntree S, Platts-Mills TA, Cogswell JJ, Mitchell EB. A subclass IgG4-specific antigen-binding radioimmunoassay (RIA): comparison between IgG and IgG4 antibodies to food and inhaled antigens in adult atopic dermatitis after desensitization treatment and during development of antibody responses in children. J Allergy Clin Immunol (1987) 80(4):622–30. doi: 10.1016/0091-6749(87)90017-0
57. Schwarz A, Panetta V, Cappella A, Hofmaier S, Hatzler L, Rohrbach A, et al. IgG and IgG4 to 91 allergenic molecules in early childhood by route of exposure and current and future IgE sensitization: Results from the multicentre allergy study birth cohort. J Allergy Clin Immunol (2016) 138(5):1426–33.e12. doi: 10.1016/j.jaci.2016.01.057
58. Wilson JM, Workman L, Schuyler AJ, Rifas-Shiman SL, McGowan EC, Oken E, et al. Allergen sensitization in a birth cohort at midchildhood: Focus on food component IgE and IgG4 responses. J Allergy Clin Immunol (2018) 141(1):419–23.e5. doi: 10.1016/j.jaci.2017.07.029
59. Devey ME, Wilson DV, Wheeler AW. The IgG subclasses of antibodies to grass pollen allergens produced in hay fever patients during hyposensitization. Clin Allergy (1976) 6(3):227–36. doi: 10.1111/j.1365-2222.1976.tb01901.x
60. van der Giessen M, Homan WL, van Kernbeek G, Aalberse RC, Dieges PH. Subclass typing of IgG antibodies formed by grass pollen-allergic patients during immunotherapy. Int Arch Allergy Appl Immunol (1976) 50(5):625–40. doi: 10.1159/000231566
61. Wisniewski J, Agrawal R, Woodfolk JA. Mechanisms of tolerance induction in allergic disease: integrating current and emerging concepts. Clin Exp Allergy (2013) 43(2):164–76. doi: 10.1111/cea.12016
62. Nowak-Węgrzyn A, Katz Y, Mehr SS, Koletzko S. Non-IgE-mediated gastrointestinal food allergy. J Allergy Clin Immunol (2015) 135(5):1114–24. doi: 10.1016/j.jaci.2015.03.025
63. Jones SM, Pons L, Roberts JL, Scurlock AM, Perry TT, Kulis M, et al. Clinical efficacy and immune regulation with peanut oral immunotherapy. J Allergy Clin Immunol (2009) 124(2):292–300.e3097. doi: 10.1016/j.jaci.2009.05.022
64. Kim EH, Bird JA, Kulis M, Laubach S, Pons L, Shreffler W, et al. Sublingual immunotherapy for peanut allergy: Clinical and immunologic evidence of desensitization. J Allergy Clin Immunol (2011) 127(3):640–6.e1. doi: 10.1016/j.jaci.2010.12.1083
65. Vickery BP, Lin J, Kulis M, Fu Z, Steele PH, Jones SM, et al. Peanut oral immunotherapy modifies IgE and IgG4 responses to major peanut allergens. J Allergy Clin Immunol (2013) 131(1):128–34.e343. doi: 10.1016/j.jaci.2012.10.048
66. Jarkvist J, Salehi C, Akin C, Gülen T. Venom immunotherapy in patients with clonal mast cell disorders: IgG4 correlates with protection. Allergy (2020) 75(1):169–77. doi: 10.1111/all.13980
67. Hesselmar B, Aberg N, Aberg B, Eriksson B, Björkstén B. Does early exposure to cat or dog protect against later allergy development? Clin Exp Allergy (1999) 29(5):611–7. doi: 10.1046/j.1365-2222.1999.00534.x
68. Renand A, Archila LD, McGinty J, Wambre E, Robinson D, Hales BJ, et al. Chronic cat allergen exposure induces a TH2 cell-dependent IgG4 response related to low sensitization. J Allergy Clin Immunol (2015) 136(6):1627–35.e13. doi: 10.1016/j.jaci.2015.07.031
69. Akdis CA, Blesken T, Akdis M, Alkan SS, Wüthrich B, Heusser CH, et al. Induction and differential regulation of bee venom phospholipase A2-specific human IgE and IgG4 antibodies in vitro requires allergen-specific and nonspecific activation of T and b cells. J Allergy Clin Immunol (1997) 99(3):345–53. doi: 10.1016/s0091-6749(97)70052-6
70. Matsui EC, Diette GB, Krop EJ, Aalberse RC, Smith AL, Curtin-Brosnan J, et al. Mouse allergen-specific immunoglobulin G and immunoglobulin G4 and allergic symptoms in immunoglobulin e-sensitized laboratory animal workers. Clin Exp Allergy (2005) 35(10):1347–53. doi: 10.1111/j.1365-2222.2005.02331.x
71. Jones M, Jeal H, Schofield S, Harris JM, Shamji MH, Francis JN, et al. Rat-specific IgG and IgG₄ antibodies associated with inhibition of IgE-allergen complex binding in laboratory animal workers. Occup Environ Med (2014) 71(9):619–23. doi: 10.1136/oemed-2014-102119
72. Stapel SO, Asero R, Ballmer-Weber BK, Knol EF, Strobel S, Vieths S, et al. Testing for IgG4 against foods is not recommended as a diagnostic tool: EAACI task force report. Allergy (2008) 63(7):793–6. doi: 10.1111/j.1398-9995.2008.01705.x
73. AAAI Board of Directors. Measurement of specific and nonspecific IgG4 levels as diagnostic and prognostic tests for clinical allergy. AAAI board of directors. J Allergy Clin Immunol (1995) 95(3):652–4.
74. Wüthrich B. Unproven techniques in allergy diagnosis. J Investig Allergol Clin Immunol (2005) 15(2):86–90.
75. Bahna SL. The dilemma of pathogenesis and diagnosis of food allergy. Immunol All Clin N Am (1987) 7:299–312. doi: 10.1016/S0889-8561(22)00474-X
76. Morgan JE, Daul CB, Lehrer SB. The relationships among shrimp-specific IgG subclass antibodies and immediate adverse reactions to shrimp challenge. J Allergy Clin Immunol (1990) 86(3 Pt 1):387–92. doi: 10.1016/s0091-6749(05)80102-2
77. Wüthrich B. Specific IgG antibodies as markers of adverse reactions to food. Contra! Monogr Allergy (1996) 32:226–7.
78. Lichtenstein LM, Kagey-Sobotka A, White JM, Hamilton RG. Anti-human IgG causes basophil histamine release by acting on IgG-IgE complexes bound to IgE receptors. J Immunol (1992) 148(12):3929–36.
79. Dannaeus A, Inganäs M. A follow-up study of children with food allergy. clinical course in relation to serum IgE- and IgG-antibody levels to milk, egg and fish. Clin Allergy (1981) 11(6):533–9. doi: 10.1111/j.1365-2222.1981.tb02171.x
80. Antico A, Pagani M, Vescovi PP, Bonadonna P, Senna G. Food-specific IgG4 lack diagnostic value in adult patients with chronic urticaria and other suspected allergy skin symptoms. Int Arch Allergy Immunol (2011) 155(1):52–6. doi: 10.1159/000318736
81. Calkhoven PG, Aalbers M, Koshte VL, Schilte PP, Yntema JL, Griffioen RW, et al. Relationship between IgG1 and IgG4 antibodies to foods and the development of IgE antibodies to inhalant allergens. II. Increased levels of IgG antibodies to foods in children who subsequently develop IgE antibodies to inhalant allergens. Clin Exp Allergy (1991) 21(1):99–107. doi: 10.1111/j.1365-2222.1991.tb00810.x
82. Eysink PE, De Jong MH, Bindels PJ, Scharp-Van Der Linden VT, De Groot CJ, Stapel SO, et al. Relation between IgG antibodies to foods and IgE antibodies to milk, egg, cat, dog and/or mite in a cross-sectional study. Clin Exp Allergy (1999) 29(5):604–10. doi: 10.1046/j.1365-2222.1999.00554.x
83. Wang XZ, Zhang HH, Qian YL, Tang LF. Sonic hedgehog (Shh) and CC chemokine ligand 2 signaling pathways in asthma. J Chin Med Assoc (2019) 82(5):343–50. doi: 10.1097/JCMA.0000000000000094
84. Engelhart S, Glynn RJ, Schur PH. Disease associations with isolated elevations of each of the four IgG subclasses. Semin Arthritis Rheumatol (2017) 47(2):276–80. doi: 10.1016/j.semarthrit.2017.03.021
85. Oka A, Ninomiya T, Fujiwara T, Takao S, Sato Y, Gion Y, et al. Serum IgG4 as a biomarker reflecting pathophysiology and post-operative recurrence in chronic rhinosinusitis. Allergol Int (2020) 69(3):417–23. doi: 10.1016/j.alit.2019.12.004
86. Koyama T, Kariya S, Sato Y, Gion Y, Higaki T, Haruna T, et al. Significance of IgG4-positive cells in severe eosinophilic chronic rhinosinusitis. Allergol Int (2019) 68(2):216–24. doi: 10.1016/j.alit.2018.09.002
87. Brouwer R, Biersteker K, Bongers P, Remijn B, Houthuijs D. Respiratory symptoms, lung function, and IgG4 levels against pig antigens in a sample of Dutch pig farmers. Am J Ind Med (1986) 10(3):283–5. doi: 10.1002/ajim.4700100314
88. Yamashita N, Ito K, Nakagawa T, Haida M, Okudaira H, Nakada S, et al. IgG and IgE antibodies to chironomidae in asthmatic patients. Clin Exp Immunol (1987) 68(1):93–9.
89. Halpern GM, Scott JR. Non-IgE antibody mediated mechanisms in food allergy. Ann Allergy (1987) 58(1):14–27.
90. Kwiatkowski L, Mitchell J, Langland J. Resolution of allergic rhinitis and reactive bronchospasm with supplements and food-specific immunoglobulin G elimination: A case report. Altern Ther Health Med (2016) 22(S3):24–8.
91. Platts-Mills TAE, Keshavarz B, Wilson JM, Li RC, Heymann PW, Gold DR, et al. An overview of the relevance of IgG4 antibodies in allergic disease with a focus on food allergens. Children (Basel) (2021) 8(5):418. doi: 10.3390/children8050418
92. Clayton F, Fang JC, Gleich GJ, Lucendo AJ, Olalla JM, Vinson LA, et al. Eosinophilic esophagitis in adults is associated with IgG4 and not mediated by IgE. Gastroenterology (2014) 147(3):602–9. doi: 10.1053/j.gastro.2014.05.036
93. Peiris CD, Tarbox JA. Eosinophilic esophagitis. JAMA (2019) 321(14):1418. doi: 10.1001/jama.2019.1992
94. Reed CC, Dellon ES. Eosinophilic esophagitis. Med Clin North Am (2019) 103(1):29–42. doi: 10.1016/j.mcna.2018.08.009
95. Lucendo AJ, Molina-Infante J, Arias Á, von Arnim U, Bredenoord AJ, Bussmann C, et al. Guidelines on eosinophilic esophagitis: Evidence-based statements and recommendations for diagnosis and management in children and adults. United Eur Gastroenterol J (2017) 5(3):335–58. doi: 10.1177/2050640616689525
96. Kelly KJ, Lazenby AJ, Rowe PC, Yardley JH, Perman JA, Sampson HA. Eosinophilic esophagitis attributed to gastroesophageal reflux: Improvement with an amino acid-based formula. Gastroenterology (1995) 109(5):1503–12. doi: 10.1016/0016-5085(95)90637-1
97. Bullock JZ, Villanueva JM, Blanchard C, Filipovich AH, Putnam PE, Collins MH, et al. Interplay of adaptive th2 immunity with eotaxin-3/c-C chemokine receptor 3 in eosinophilic esophagitis. J Pediatr Gastroenterol Nutr (2007) 45(1):22–31. doi: 10.1097/MPG.0b013e318043c097
98. Lucendo AJ, Lucendo B. An update on the immunopathogenesis of eosinophilic esophagitis. Expert Rev Gastroenterol Hepatol (2010) 4(2):141–8. doi: 10.1586/egh.10.9
99. Lucendo AJ. Cellular and molecular immunological mechanisms in eosinophilic esophagitis: an updated overview of their clinical implications. Expert Rev Gastroenterol Hepatol (2014) 8(6):669–85. doi: 10.1586/17474124.2014.909727
100. Wright BL, Kulis M, Guo R, Orgel KA, Wolf WA, Burks AW, et al. Food-specific IgG4 is associated with eosinophilic esophagitis. J Allergy Clin Immunol (2016) 138(4):1190–2.e3. doi: 10.1016/j.jaci.2016.02.024
101. Peterson K, Lin E, Saffari H, Qeadan F, Pyne A, Firszt R, et al. Food-specific antibodies in oesophageal secretions: association with trigger foods in eosinophilic oesophagitis. Aliment Pharmacol Ther (2020) 52(6):997–1007. doi: 10.1111/apt.15879
102. Schuyler AJ, Wilson JM, Tripathi A, Commins SP, Ogbogu PU, Kruzsewski PG, et al. Specific IgG4 antibodies to cow's milk proteins in pediatric patients with eosinophilic esophagitis. J Allergy Clin Immunol (2018) 142(1):139–48.e12. doi: 10.1016/j.jaci.2018.02.049
103. Burk CM, Dellon ES, Steele PH, Virkud YV, Kulis M, Burks AW, et al. Eosinophilic esophagitis during peanut oral immunotherapy with omalizumab. J Allergy Clin Immunol Pract (2017) 5(2):498–501. doi: 10.1016/j.jaip.2016.11.010
104. Anagusko CLY, Mendonca J, Lopes MM, Torres P, Torres CSF, Castro FM, et al. Specific IgG4 to milk proteins during oral immunotherapy for milk allergy: Relationship to eosinophilic esophagitis. J. Allergy Clin Immunol (2019) 143:Ab138. doi: 10.1016/j.jaci.2018.12.419
105. Kleine-Tebbe J, Waßmann-Otto A, Mönnikes H. Nahrungsmittelallergien und andere -unverträglichkeiten: Bedeutung, begriffe und begrenzung [Food allergy and intolerance: Distinction, definitions and delimitation]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz (2016) 59(6):705–22. doi: 10.1007/s00103-016-2356-1
Keywords: IgG4, Fab-arm exchange, allergen specific immunotherapy, food allergy, eosinophilic esophagitis
Citation: Qin L, Tang L-F, Cheng L and Wang H-Y (2022) The clinical significance of allergen-specific IgG4 in allergic diseases. Front. Immunol. 13:1032909. doi: 10.3389/fimmu.2022.1032909
Received: 31 August 2022; Accepted: 20 September 2022;
Published: 25 October 2022.
Edited by:
Jiong Chen, Ningbo University, ChinaReviewed by:
Xinguo Jiang, Stanford University, United StatesQintai Yang, Sun Yat-sen University, China
Lianyun Wang, Shanghai Jiao Tong University, China
Copyright © 2022 Qin, Tang, Cheng and Wang. 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: Hui-Ying Wang, bWFyeXdhbmdAemp1LmVkdS5jbg==; Lei Cheng, Y2hlbmdsZWlAanNwaC5vcmcuY24=
†These authors have contributed equally to this work