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Functional Fcgamma Receptor Polymorphisms Are Associated with Human Allergy

  • Jianming Wu ,

    jmwu@umn.edu

    Affiliations Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, Minnesota, United States of America, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, United States of America

  • Rui Lin,

    Affiliation Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, Minnesota, United States of America

  • Jinhai Huang,

    Affiliation Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, Minnesota, United States of America

  • Weihua Guan,

    Affiliation Department of Biostatistics, University of Minnesota, Minneapolis, Minnesota, United States of America

  • William S. Oetting,

    Affiliation Department of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota, United States of America

  • P. Sriramarao,

    Affiliations Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, Minnesota, United States of America, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, United States of America

  • Malcolm N. Blumenthal

    Affiliation Department of Medicine, University of Minnesota, Minneapolis, Minnesota, United States of America

Functional Fcgamma Receptor Polymorphisms Are Associated with Human Allergy

  • Jianming Wu, 
  • Rui Lin, 
  • Jinhai Huang, 
  • Weihua Guan, 
  • William S. Oetting, 
  • P. Sriramarao, 
  • Malcolm N. Blumenthal
PLOS
x

Abstract

Objective

IgG Fc receptors (FcγRs) play important roles in immune responses. It is not clear whether FcγR receptors play a role in human asthma and allergy. The aim of current study was to investigate whether functional single nucleotide polymorphisms (SNPs) of FcγR genes (FCGR) are associated with human asthma and allergy.

Methods

Functional SNPs of FCGR2A (FcγRIIA-131His>Arg, rs1801274), FCGR2B (FcγRIIB-187Ile>Thr, rs1050501), FCGR2C (FcγRIIC-13Gln>Stop, rs10917661), FCGR3A (FcγRIIIA-158Val>Phe, rs396991), and FCGR3B variants (FcγRIIIB NA1 and NA2) were genotyped in an asthma family cohort including 370 atopy positive, 239 atopy negative, and 169 asthma positive subjects. The genotype and phenotype data (asthma, bronchial hyper-responsiveness, and atopy) of subjects were analyzed using family-based association tests (FBAT) and logistic regression adjusted for age and sex.

Result

The FcγRIIA-131His>Arg SNP is significantly associated with atopy in a family-based association test (P = 0.00287) and in a logistic regression analysis (P = 0.0269, OR 0.732, 95% CI: 0.555–0.965). The FcγRIIA-131His (or rs1801274-A) allele capable of binding human IgG2 has a protective role against atopy. In addition, the rare FcγRIIB-187Thr (or rs1050501-C) allele defective for the receptor-mediated inhibitory signals is a risk factor for atopy (P = 0.0031, OR 1.758, 95% CI: 1.209–2.556) and IgE production (P<0.001). However, variants of activating FcγRIIIA (rs396991), and FcγRIIIB (NA1 and NA2), and FcγRIIC (rs10917661) are not associated with asthma, BHR, and atopy (P>0.05).

Conclusions

FcγRIIA and FcγRIIB functional polymorphisms may have a role in the pathogenesis of allergy.

Introduction

Asthma is a complex syndrome characterized by airflow obstruction, bronchial hyper-responsiveness (BHR), and airway inflammation. Both genetic and environmental factors contribute to the development of asthma. Evidence for a genetic component in asthma includes familial clustering and higher concordance rates in monozygotic twins than in dizygotic twins [1], [2]. Approximately 48–79% of asthma risk is attributable to genetic factors [1], [2]. According to the American Academy of Allergy, Asthma and Immunology, half of the 20 million Americans with asthma have allergic asthma. Thus, allergic reactions to foreign antigens are considered as the most common causes for asthma. To date, no genes have been definitely shown to influence asthma/allergy development. It is well-known that IgE and its cognate receptor (FcεRI) are important mediators in allergic reactions [3]. However, the role of human IgG Fc receptors (FcγRs) in asthma and allergy remains unknown.

A recent meta-analysis of human genome-wide association study (GWAS) revealed a significant asthma susceptibility locus on chromosome 1q23, where FcγR (FCGR) genes are located [4]. Human FcγRs are glycoproteins that bind the Fc region of immunoglobulin G (IgG). FcγRs mediate a variety of immune functions such as antigen presentation, immune complex clearance, phagocytosis of pathogens, degranulations, ADCC, and cytokine production [5]. In humans, five genes (FCGR2A, FCGR2B, FCGR2C, FCGR3A, and FCGR3B) in the 1q23 chromosome region code for five classical low affinity Fcγ receptors (FcγRIIA, FcγRIIB, FcγRIIC, FcγRIIIA, and FcγRIIIB). Coordination between the activating FcγRs (FcγRIIA, FcγRIIC, FcγRIIIA, and FcγRIIIB) and the inhibitory FcγR (FcγRIIB) is crucial in balancing immune responses and determining the outcomes of local and systemic inflammations [6]. FcγRs have important roles in the pathogenesis of a variety of human inflammatory diseases [7]. Not surprisingly, functional polymorphisms of FcγR have robust effects on susceptibility and severity of inflammatory diseases as demonstrated in genetic association studies by our group and others [8], [9], [10], [11]. However, comprehensive genetic analysis of human FCGR genes in asthma/allergy patients has yet been performed. It remains unknown whether human FcγRs play a role in the development of allergy.

Patients and Methods

Study Subjects

Genomic DNA was isolated from anti-coagulated peripheral blood of human subjects from 27 multigenerational families with multiple asthmatic members, which were originally recruited as part of the Collaborative Study on the Genetics of Asthma (CSGA) [12]. For the CSGA, asthma families were ascertained through two asthmatic siblings. Additional relatives in the families were then recruited either by extending the families through asthmatic relatives or by including no more than one unaffected relative to permit a lineage to incorporate other relatives with asthma. The inclusion criteria for each family consisted of each of the two asthmatic siblings having met the following criteria for the proband: (1) being at least 6 years of age; (2) having either bronchial hyper-responsiveness (BHR), defined as a fall from baseline FEV1 greater than 20% in one second after inhalation of 25 mg/ml or less of methacholine, or reversibility, defined as a 15% or greater increase from baseline FEV1 after inhaled bronchodilator (albuterol) for those with reduced baseline FEV1; (3) having the presence of two or more of the symptoms of coughing, wheezing and shortness of breath; (4) having less than three pack/years of cigarette smoking; and (5) having a physician’s diagnosis of asthma with no conflicting pulmonary disease. All family members went through a standardized protocol consisting of an interviewer administered questionnaire, pulmonary function studies including a methacholine challenge and/or reversibility studies, blood drawing for serum IgE levels at a single time not during an acute exacerbation and skin prick testing using standardized allergens [12]. Additional details of the study design can be found in an earlier publication [12]. The 27 multigenerational Caucasian families were recruited in Minnesota as previously described [13]. These families had 169 asthmatic members, 347 who were not asthmatic and 129 for whom the diagnosis was unavailable [13]. Pulmonary function data were available on 619 individuals. The study (Title: Genetics of Asthma. Study Number: 920M05150) was approved by The Institutional Review Board of Human Study at the University Of Minnesota. The informed written consent was obtained from all participants recruited in this study. The written consents containing participants’ signatures were kept in locked file cabinets for record. The traits of asthma, BHR, atopy, and IgE levels were analyzed in the current genetic study.

Genotyping of FCGR SNPs

FCGR family member genes were generated through duplication and divergence during evolution [14]. SNPs in five FCGR genes are not suitable for direct TaqMan assays due to near 100% sequence identity surrounding the functional SNPs between homologous genes. Consequently, we used a modified FCGR SNP TaqMan assay in which FCGR gene-specific PCR fragments were used as templates instead of genomic DNA for TaqMan assays. The genomic DNA fragments containing functional SNPs of FCGR2A and FCGR3A were amplified using the gene specific primers as described previously [9]. For the FCGR2B SNP, a genomic DNA fragment containing FcγRIIB-187Ile>Thr was amplified using the gene specific primers as described [8], [15]. To genotype FcγRIIC-13Gln>STP, a long FCGR2C genomic fragment (6227 bps) containing the SNP was amplified using Platinum Taq DNA Polymerase High Fidelity (Invitrogen) with a sense primer (5′-CTG CAT ATG TTG TCC CCC TGT GTT GCT AAA T-3′) annealing to the FCGR2C intron 2 and an antisense primer (5′-AAC ATG AGA GAG AAA AAG AGA GGC AGG GAG GGA GCT TA-3′) annealing to the FCGR2C intron 6. The TaqMan assays for FCGR2A SNP (FcγRIIA-131His>Arg), FCGR2B SNP (FcγRIIB-187Ile>Thr), FCGR2C SNP (FcγRIIC-13Gln>STP), and FCGR3A SNP (FcγRIIIA-158Val>Phe) were designed using the Software Primer Express v3.0 (Applied Biosystems Inc.). TaqMan genotyping assays were carried out according to the standard protocol on an ABI 7500 Real-Time PCR System using Genotyping Master Mix (Applied Biosystems). The primers and probes used in FCGR TaqMan genotyping assays are listed in Table 1. Genotyping of the respective SNPs of FCGR2A, FCGR2B, FCGR2C, and FCGR3A was carried out with four independent TaqMan allele discrimination assays that were developed and validated in the lab. The specificity and accuracy of individual TaqMan assays were validated by the perfect match (100%) with at least 300 genotyped human subjects published previously [8], [9], [15]. For FCGR3B allele determination, a primer pair that specifically amplifies the FCGR3B fragment containing FCGR3B coding SNPs (cSNPs) was used. The 1.6 kb FCGR3B PCR fragment was treated with ExoSAP-IT PCR Product Clean-UP reagent (Affymetrix) before being sequenced on an ABI 3730xl DNA Analyzer with BigDye Terminator kit (Applied Biosystems) with the sequencing primer (5′-TCC TCA CCC CAC ATT ATC TTG-3′). The FCGR3B alleles and genotypes were determined based on the published reference [16], [17].

Statistical Analysis

The IgE levels were log-transformed to correct for skewed distribution. Family-based association tests (FBAT) [18] were used to examine whether individual FCGR SNPs are associated with phenotypes of human subjects in the asthma family cohort. Alternatively, we used conditional logistic regression to estimate odds ratios of FCGR SNPs for their association with asthma, BHR, and atopy, adjusting for age and sex. The association between log-transformed IgE levels and FCGR genotypes were analyzed using one-way analysis of variance (ANOVA) in addition to the nonparametric t-test (Mann-Whitney test). In both FBAT and regression analysis, an additive model was assumed for SNP genotypes. To correct for multiple hypothesis tests, the Bonferroni method was used and the null hypothesis was reject at 0.05/number of tests.

Results

The FcγRIIA SNP is Associated with Atopy

As shown in Table 2, the FCGR2A SNP (FcγRIIA-131His>Arg, rs1801274) is significantly associated with atopy in the family-based association test (FBAT) (P = 0.003). The FCGR2A SNP is also associated with asthma and BHR in FBAT (P<0.05). Conditional logistic regression analysis estimated an OR of 0.732 (P = 0.027, 95% CI: 0.555–0.965) for FCGR2A SNP with atopy, suggesting a protective role against atopy for carriers of the FcγRIIA-131His allele (population allele frequency = 0.488). Although the FCGR2A SNP is significantly associated with asthma and BHR in FBAT (P<0.05), the association were not significant in logistic regression analyses adjusted for age and sex. Further validation may be needed to confirm our findings. Furthermore, the functional SNPs of the other three activating FcγRs (FcγRIIIA, FcγRIIIB, and FcγRIIC) were not associated with asthma, BHR, and atopy (P>0.05) (Table 3).

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Table 3. Functional SNPs of FCGR3A, FCGR3B, and FCGR2C are not associated with asthma, BHR, and atopy.

https://doi.org/10.1371/journal.pone.0089196.t003

The Inhibitory FcγRIIB SNP is Associated with Atopy and IgE Production

Although the FCGR2B SNP (FcγRIIB-187Ile>Thr, rs1050501) is not associated with asthma, BHR, and atopy in FBAT analyses, conditional logistic regression analyses showed that FCGR2B SNP is significantly associated with atopy and that the FcγRIIB-187Thr (allele frequency = 0.088) is a risk allele for atopy (P = 0.003, OR 1.758, 95% CI: 1.209–2.556) (Table 2). Because immunoglobulin E (IgE) play an important role in allergic diseases and elevated total IgE is frequently considered as a diagnostic criterion for allergic diseases [3], we subsequently analyzed whether the FcγRIIB SNP is associated with IgE levels in human subjects. As shown in Figure 1A, FcγRIIB genotypes are significantly associated with the serum IgE levels. The human subjects carrying rare FcγRIIB-Thr allele produced significantly more IgE (P = 0.0002 for 187Ile/Thr heterozygous subjects and P = 0.0004 for 187Thr/Thr homozygous subjects) than those homozygous (187-Ile/Ile) subjects carrying the common allele, suggesting that the functional FcγRIIB SNP may have a role in allergy through IgE production. On the other hand, FcγRIIA SNP is not associated with IgE production in humans (Figure 1B).

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Figure 1. Association of SNP FCGR2B-187Ile>Thr with IgE levels.

A. The genotypes of FCGR2B-187Ile>Thr were significantly associated with IgE levels in ANOVA (P<0.0001). The rare FCGR2B-187Thr carriers (187Ile/Thr and 187Thr/Thr genotypes) produced significantly more IgE than the homozygous subjects for common allele (187Ile) in Mann-Whitney tests. B. The genotypes of FCGR2B-131His>Arg were not associated with IgE levels in ANOVA (P = 0.817). No significant differences were found between FCGR2A-131Arg carriers (131his/Arg and 131Arg/Arg genotypes) and the 131His homozygous subjects in Mann-Whitney tests (P>0.05).

https://doi.org/10.1371/journal.pone.0089196.g001

Discussion

This study shows the association of two functional SNPs (the activating FcγRIIA-131His>Arg and the inhibitory FcγRIIB-187Ile>Thr) with human atopy. Furthermore, we demonstrated an association between FcγRIIB SNP and IgE production. Our data indicate a role for IgG Fc receptors in the development of allergy.

FcγRIIA is expressed on the surface of various immune cells including mast cells, basophils, neutrophils, monocytes, dendritic cells, macrophages, and platelets [19], [20]. The FcγRIIA-131His>Arg SNP significantly affects receptor binding affinity and specificity for IgG subclasses [21], [22]. Although both FcγRIIA-131His and 131Arg alleles bind IgG1 and IgG3, the FcγRIIA-131His allele displays a higher binding affinity for IgG3 and is capable of binding IgG2 most effectively as compared to the FcγRIIA-131Arg allele [21], [22]. The functional FcγRIIA-131His>Arg SNP affects the receptor binding affinity for IgG and thus influences the clinical phenotype in response to infectious diseases and inflammation [21]. The FcγRIIA-131His>Arg SNP affects the functions of bacterial phagocytosis [23], [24] and immune complex handling [22], [25], [26]. The FcγRIIA-131His>Arg SNP has been reported to be associated with ulcerative colitis [27], Kawasaki diseases [28], systemic lupus erythematosus [29], and chronic inflammatory disorders such as periodontitis [30], [31] and Guillain-Barré syndrome [32]. In addition, FcγRIIA-131His>Arg polymorphism is associated with infections including recurrent bacterial respiratory tract infections [33], bacteremic pneumococcal pneumonia [34], severe acute respiratory syndrome [35], severe sepsis [36], HIV [37], and EB virus infection [38]. IgG2 is produced primarily in response to polysaccharide/carbohydrate antigens commonly found in allergens. The protective effect of the FcγRIIA-131His allele on atopy is possibly due to the increased capacity of this allele to efficiently internalize and destroy allergen-IgG2 immune complexes. The role of FcγRIIA in allergy was also demonstrated in transgenic mouse models [39]. Therefore, FcγRIIA likely contributes to allergy development in humans. Although the FcγRIIA-131His>Arg SNP is associated with atopy, the SNP is not associated with IgE production (Figure 1B), suggesting that FcγRIIA likely affects allergy through pathways of immune complex clearance and receptor-mediated cell activation. Future studies are required to reveal whether IgG2 levels are associated with the asthma or atopy in the context of FcγRIIA SNP and whether FcγRIIA-mediated functions (immune complex clearance and phagocytosis of allergens) are different between asthmatic and non-asthmatic human subjects.

FcγRIIB, mainly expressed on B cells and myeloid cells, is a classical inhibitory IgG Fc receptor [40], [41], [42]. Cross-linking of FcγRIIB by immune complexes leads to the down-regulation of B cell activation and antibody production, which is an important feedback mechanism to maintain the homeostasis of immune responses [5], [40], [43]. Therefore, FcγRIIB overexpression (or enhanced FcγRIIB functions) reduces the immunoglobulin production in T-dependent immune responses [44]. In humanized mouse models of immunoglobulin production, co-engagement of IgE B-cell receptor with FcγRIIB drastically inhibited human IgE production [45]. FcγRIIB-187Ile>Thr SNP (rs1050501) is located within the receptor transmembrane segment and the FcγRIIB-187Thr allele is less efficient in mediating inhibitory signals than the FcγRIIB-187Ile allele [46], [47], [48]. We observed that the low function FcγRIIB-187Thr allele is significantly associated with elevated IgE levels (Figure 1), suggesting that the reduced FcγRIIB function may promote IgE antibody production by B cells in humans. Interestingly, the low function FcγRIIB-187Thr allele is also associated with protection against malaria [49], signifying FcγRIIB functions play important roles in controlling the immune response to parasites [50]. Nevertheless, FcγRIIB-187Ile>Thr SNP may also be in linkage equilibrium with SNPs of the FCER1A gene encoding for the alpha chain of the high affinity receptor for IgE (FcεRIA) because a GWAS identified the FCER1A functional variants strongly associated with total IgE levels [51].

FcγRIIB on immune cells also inhibits cellular functions including phagocytosis, ADCC, degranulation, and cytokine release [40]. Mast cells from FcγRIIB−/− mice are highly sensitive to IgG-triggered degranulation compared to those from the wild-type mice. FcγRIIB-deficient mice have an enhanced passive cutaneous analphylaxis reaction, as a result of the decreased threshold for mast-cell activation through activating Fc receptors [52]. FcγRIIB negatively regulates cell activation triggered by high-affinity IgE receptors (FcεRI) [53]. FcγRIIB binds to the Fc domains of IgE and IgG with similar low affinity [54], [55]. Mast cells and basophils could be regulated by immune complexes of allergen–IgG or allergen–IgE. FcγRIIB-deficient mice developed more severe eosinophilia compared to wild-type mice, suggesting an important regulatory role for FcγRIIB in the onset of allergic diseases [56]. FcγRIIB-knockout mice developed the exacerbated lung inflammation [57]. Taken together, FcγRIIB seems to play a critical role in allergic inflammations. In the current study, the dysfunctional FcγRIIB-187Thr allele was found to be a risk factor for atopy. A decreased activation threshold for immune cells carrying FcγRIIB-187Thr allele may be responsible for the increased sensitivity to allergens that trigger the allergic responses, which may explain the association between the defective FcγRIIB allele and atopy.

On the other hand, the functional SNPs of the other three activating FcγRs (FcγRIIIA, FcγRIIIB, and FcγRIIC) were not associated with asthma, BHR, and atopy, suggesting that functions of the restrictively expressed activating FcγRs (FcγRIIIA, FcγRIIIB, and FcγRIIC) may not play prevailing roles in the development of allergy. Our current study had more than 80% power to detect an association between a FCGR SNP and atopy with an OR of 1.75.

In summary, the functional SNPs of FcγRIIA and FcγRIIB are associated with atopy, signifying that FcγRIIA and FcγRIIB may serve as important modifiers in the development of allergy. Therefore, targeting FcγRIIA and FcγRIIB for enhanced receptor expressions and functions may be an important avenue for therapeutic discovery in allergy and asthma treatment.

Supporting Information

Table S1.

Distribution of FCGR2A SNP (rs1801274) in atopy+ and atopy- subjects.

https://doi.org/10.1371/journal.pone.0089196.s001

(DOC)

Table S2.

Distribution of FCGR2B SNP (rs1050501) in atopy+ and atopy- subjects.

https://doi.org/10.1371/journal.pone.0089196.s002

(DOC)

Author Contributions

Conceived and designed the experiments: JW WSO PS MNB. Performed the experiments: JW RL JH WG WSO MNB. Analyzed the data: JW RL JH WG WSO PS MNB. Contributed reagents/materials/analysis tools: WG WSO MNB. Wrote the paper: JW WG WSO MNB.

References

  1. 1. Duffy DL, Martin NG, Battistutta D, Hopper JL, Mathews JD (1990) Genetics of asthma and hay fever in Australian twins. Am Rev Respir Dis 142: 1351–1358.
  2. 2. Nieminen MM, Kaprio J, Koskenvuo M (1991) A population-based study of bronchial asthma in adult twin pairs. Chest 100: 70–75.
  3. 3. Galli SJ, Tsai M (2012) IgE and mast cells in allergic disease. Nat Med 18: 693–704.
  4. 4. Torgerson DG, Ampleford EJ, Chiu GY, Gauderman WJ, Gignoux CR, et al. (2011) Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nat Genet 43: 887–892.
  5. 5. Ravetch JV, Bolland S (2001) IgG Fc receptors. Annu Rev Immunol 19: 275–290.
  6. 6. Boruchov AM, Heller G, Veri MC, Bonvini E, Ravetch JV, et al. (2005) Activating and inhibitory IgG Fc receptors on human DCs mediate opposing functions. J Clin Invest 115: 2914–2923.
  7. 7. Takai T (2002) Roles of Fc receptors in autoimmunity. Nat Rev Immunol 2: 580–592.
  8. 8. Chen JY, Wang CM, Ma CC, Luo SF, Edberg JC, et al. (2006) Association of a transmembrane polymorphism of Fcgamma receptor IIb (FCGR2B) with systemic lupus erythematosus in Taiwanese patients. Arthritis Rheum 54: 3908–3917.
  9. 9. Edberg JC, Langefeld CD, Wu J, Moser KL, Kaufman KM, et al. (2002) Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus. Arthritis Rheum 46: 2132–2140.
  10. 10. Morgan AW, Griffiths B, Ponchel F, Montague BM, Ali M, et al. (2000) Fcgamma receptor type IIIA is associated with rheumatoid arthritis in two distinct ethnic groups. Arthritis Rheum 43: 2328–2334.
  11. 11. Wu J, Edberg JC, Redecha PB, Bansal V, Guyre PM, et al. (1997) A novel polymorphism of FcgammaRIIIa (CD16) alters receptor function and predisposes to autoimmune disease. J Clin Invest 100: 1059–1070.
  12. 12. A genome-wide search for asthma susceptibility loci in ethnically diverse populations. The Collaborative Study on the Genetics of Asthma (CSGA). Nat Genet 15: 389–392.
  13. 13. Reilly C, Miller MB, Liu Y, Oetting WS, King R, et al. (2007) Linkage analysis of a cluster-based quantitative phenotype constructed from pulmonary function test data in 27 multigenerational families with multiple asthmatic members. Hum Hered 64: 136–145.
  14. 14. Qiu WQ, de Bruin D, Brownstein BH, Pearse R, Ravetch JV (1990) Organization of the human and mouse low-affinity Fc gamma R genes: duplication and recombination. Science 248: 732–735.
  15. 15. Chen JY, Wang CM, Ma CC, Hsu LA, Ho HH, et al. (2008) A transmembrane polymorphism in FcgammaRIIb (FCGR2B) is associated with the production of anti-cyclic citrullinated peptide autoantibodies in Taiwanese RA. Genes Immun 9: 680–688.
  16. 16. Ory PA, Clark MR, Kwoh EE, Clarkson SB, Goldstein IM (1989) Sequences of complementary DNAs that encode the NA1 and NA2 forms of Fc receptor III on human neutrophils. J Clin Invest 84: 1688–1691.
  17. 17. Ory PA, Goldstein IM, Kwoh EE, Clarkson SB (1989) Characterization of polymorphic forms of Fc receptor III on human neutrophils. J Clin Invest 83: 1676–1681.
  18. 18. Laird NM, Horvath S, Xu X (2000) Implementing a unified approach to family-based tests of association. Genet Epidemiol 19 Suppl 1S36–42.
  19. 19. Takai T (2005) Fc receptors and their role in immune regulation and autoimmunity. J Clin Immunol 25: 1–18.
  20. 20. Rascu A, Repp R, Westerdaal NA, Kalden JR, van de Winkel JG (1997) Clinical relevance of Fc gamma receptor polymorphisms. Ann N Y Acad Sci 815: 282–295.
  21. 21. Bruhns P, Iannascoli B, England P, Mancardi DA, Fernandez N, et al. (2009) Specificity and affinity of human Fcgamma receptors and their polymorphic variants for human IgG subclasses. Blood 113: 3716–3725.
  22. 22. Warmerdam PA, van de Winkel JG, Vlug A, Westerdaal NA, Capel PJ (1991) A single amino acid in the second Ig-like domain of the human Fc gamma receptor II is critical for human IgG2 binding. J Immunol 147: 1338–1343.
  23. 23. Sanders LA, Feldman RG, Voorhorst-Ogink MM, de Haas M, Rijkers GT, et al. (1995) Human immunoglobulin G (IgG) Fc receptor IIA (CD32) polymorphism and IgG2-mediated bacterial phagocytosis by neutrophils. Infect Immun 63: 73–81.
  24. 24. Bredius RG, de Vries CE, Troelstra A, van Alphen L, Weening RS, et al. (1993) Phagocytosis of Staphylococcus aureus and Haemophilus influenzae type B opsonized with polyclonal human IgG1 and IgG2 antibodies. Functional hFc gamma RIIa polymorphism to IgG2. J Immunol 151: 1463–1472.
  25. 25. Salmon JE, Edberg JC, Brogle NL, Kimberly RP (1992) Allelic polymorphisms of human Fc gamma receptor IIA and Fc gamma receptor IIIB. Independent mechanisms for differences in human phagocyte function. J Clin Invest 89: 1274–1281.
  26. 26. Salmon JE, Millard S, Schachter LA, Arnett FC, Ginzler EM, et al. (1996) Fc gamma RIIA alleles are heritable risk factors for lupus nephritis in African Americans. J Clin Invest 97: 1348–1354.
  27. 27. Asano K, Matsushita T, Umeno J, Hosono N, Takahashi A, et al. (2009) A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. Nat Genet 41: 1325–1329.
  28. 28. Khor CC, Davila S, Breunis WB, Lee YC, Shimizu C, et al. (2011) Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease. Nat Genet 43: 1241–1246.
  29. 29. Harley JB, Alarcon-Riquelme ME, Criswell LA, Jacob CO, Kimberly RP, et al. (2008) Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. Nat Genet 40: 204–210.
  30. 30. Yamamoto K, Kobayashi T, Grossi S, Ho AW, Genco RJ, et al. (2004) Association of Fcgamma receptor IIa genotype with chronic periodontitis in Caucasians. J Periodontol 75: 517–522.
  31. 31. Chai L, Song YQ, Leung WK (2012) Genetic polymorphism studies in periodontitis and Fcgamma receptors. J Periodontal Res 47: 273–285.
  32. 32. van der Pol WL, van den Berg LH, Scheepers RH, van der Bom JG, van Doorn PA, et al. (2000) IgG receptor IIa alleles determine susceptibility and severity of Guillain-Barre syndrome. Neurology 54: 1661–1665.
  33. 33. Sanders LA, van de Winkel JG, Rijkers GT, Voorhorst-Ogink MM, de Haas M, et al. (1994) Fc gamma receptor IIa (CD32) heterogeneity in patients with recurrent bacterial respiratory tract infections. J Infect Dis 170: 854–861.
  34. 34. Yee AM, Phan HM, Zuniga R, Salmon JE, Musher DM (2000) Association between FcgammaRIIa-R131 allotype and bacteremic pneumococcal pneumonia. Clin Infect Dis 30: 25–28.
  35. 35. Yuan FF, Tanner J, Chan PK, Biffin S, Dyer WB, et al. (2005) Influence of FcgammaRIIA and MBL polymorphisms on severe acute respiratory syndrome. Tissue Antigens 66: 291–296.
  36. 36. Endeman H, Cornips MC, Grutters JC, van den Bosch JM, Ruven HJ, et al. (2009) The Fcgamma receptor IIA-R/R131 genotype is associated with severe sepsis in community-acquired pneumonia. Clin Vaccine Immunol 16: 1087–1090.
  37. 37. Forthal DN, Landucci G, Bream J, Jacobson LP, Phan TB, et al. (2007) FcgammaRIIa genotype predicts progression of HIV infection. J Immunol 179: 7916–7923.
  38. 38. Diamantopoulos PT, Kalotychou V, Polonyfi K, Sofotasiou M, Anastasopoulou A, et al. (2013) Correlation of Fc-gamma RIIA polymorphisms with latent Epstein-Barr virus infection and latent membrane protein 1 expression in patients with low grade B-cell lymphomas. Leuk Lymphoma 54: 2030–2034.
  39. 39. Jonsson F, Mancardi DA, Zhao W, Kita Y, Iannascoli B, et al. (2012) Human FcgammaRIIA induces anaphylactic and allergic reactions. Blood 119: 2533–2544.
  40. 40. Ravetch JV, Lanier LL (2000) Immune inhibitory receptors. Science 290: 84–89.
  41. 41. Muta T, Kurosaki T, Misulovin Z, Sanchez M, Nussenzweig MC, et al. (1994) A 13-amino-acid motif in the cytoplasmic domain of Fc gamma RIIB modulates B-cell receptor signalling. Nature 368: 70–73.
  42. 42. Xiang Z, Cutler AJ, Brownlie RJ, Fairfax K, Lawlor KE, et al. (2007) FcgammaRIIb controls bone marrow plasma cell persistence and apoptosis. Nat Immunol 8: 419–429.
  43. 43. Cohen-Solal JF, Cassard L, Fridman WH, Sautes-Fridman C (2004) Fc gamma receptors. Immunol Lett 92: 199–205.
  44. 44. Brownlie RJ, Lawlor KE, Niederer HA, Cutler AJ, Xiang Z, et al. (2008) Distinct cell-specific control of autoimmunity and infection by FcgammaRIIb. J Exp Med 205: 883–895.
  45. 45. Chu SY, Horton HM, Pong E, Leung IW, Chen H, et al. (2012) Reduction of total IgE by targeted coengagement of IgE B-cell receptor and FcgammaRIIb with Fc-engineered antibody. J Allergy Clin Immunol 129: 1102–1115.
  46. 46. Li X, Wu J, Carter RH, Edberg JC, Su K, et al. (2003) A novel polymorphism in the Fcgamma receptor IIB (CD32B) transmembrane region alters receptor signaling. Arthritis Rheum 48: 3242–3252.
  47. 47. Kono H, Kyogoku C, Suzuki T, Tsuchiya N, Honda H, et al. (2005) Fc{gamma}RIIB Ile232Thr transmembrane polymorphism associated with human systemic lupus erythematosus decreases affinity to lipid rafts and attenuates inhibitory effects on B cell receptor signaling. Hum Mol Genet 14: 2881–2892.
  48. 48. Floto RA, Clatworthy MR, Heilbronn KR, Rosner DR, Macary PA, et al. (2005) Loss of function of a lupus-associated FcgammaRIIb polymorphism through exclusion from lipid rafts. Nat Med 11: 1056–1058.
  49. 49. Willcocks LC, Carr EJ, Niederer HA, Rayner TF, Williams TN, et al. (2010) A defunctioning polymorphism in FCGR2B is associated with protection against malaria but susceptibility to systemic lupus erythematosus. Proc Natl Acad Sci U S A 107: 7881–7885.
  50. 50. Clatworthy MR, Willcocks L, Urban B, Langhorne J, Williams TN, et al. (2007) Systemic lupus erythematosus-associated defects in the inhibitory receptor FcgammaRIIb reduce susceptibility to malaria. Proc Natl Acad Sci U S A 104: 7169–7174.
  51. 51. Weidinger S, Gieger C, Rodriguez E, Baurecht H, Mempel M, et al. (2008) Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus. PLoS Genet 4: e1000166.
  52. 52. Takai T, Ono M, Hikida M, Ohmori H, Ravetch JV (1996) Augmented humoral and anaphylactic responses in Fc gamma RII-deficient mice. Nature 379: 346–349.
  53. 53. Malbec O, Attal JP, Fridman WH, Daeron M (2002) Negative regulation of mast cell proliferation by FcgammaRIIB. Mol Immunol 38: 1295–1299.
  54. 54. Takizawa F, Adamczewski M, Kinet JP (1992) Identification of the low affinity receptor for immunoglobulin E on mouse mast cells and macrophages as Fc gamma RII and Fc gamma RIII. J Exp Med 176: 469–475.
  55. 55. Ujike A, Ishikawa Y, Ono M, Yuasa T, Yoshino T, et al. (1999) Modulation of immunoglobulin (Ig)E-mediated systemic anaphylaxis by low-affinity Fc receptors for IgG. J Exp Med 189: 1573–1579.
  56. 56. Watanabe T, Okano M, Hattori H, Yoshino T, Ohno N, et al. (2004) Roles of FcgammaRIIB in nasal eosinophilia and IgE production in murine allergic rhinitis. Am J Respir Crit Care Med 169: 105–112.
  57. 57. Dharajiya N, Vaidya SV, Murai H, Cardenas V, Kurosky A, et al. (2010) FcgammaRIIb inhibits allergic lung inflammation in a murine model of allergic asthma. PLoS One 5: e9337.