Skip to main content
Download PDF
  • Research note
  • Open access
  • Published:

Impacts of FcγRIIB and FcγRIIIA gene polymorphisms on systemic lupus erythematous disease activity index

BMC Research Notes volume 14, Article number: 455 (2021) Cite this article

A Correction to this article was published on 14 July 2022

This article has been updated

Abstract

Objective

Systemic lupus erythematous (SLE) disease is a chronic autoimmune disease with unknown etiology that can involve different organs. Polymorphisms in Fcγ receptors have been identified as genetic factors in susceptibility to SLE. This study was aimed to investigate effects of two single nucleotide polymorphisms (SNPs) within FcγRIIB and FcγRIIIA genes on systemic lupus erythematous disease activity index (SLEDAI) in an Iranian population.

Results

Our findings indicated TT and GG genotypes were the common genotypes of FcγRIIB and FcγRIIIA SNPs in SLE patients, respectively. There were no significant differences in genotype and allele frequencies of FcγRIIB and FcγRIIIA SNPs in SLE and healthy subjects. However, the frequencies of genotypes and alleles of FcγRIIB and FcγRIIIA SNPs were significantly associated with some clinical manifestations used to determine SLEDAI (P < 0.001–0.5).

Introduction

Systemic lupus erythematosus (SLE) is a systemic autoimmune disease with unknown etiology described by the lack of immunological tolerance to self-antigens, atypical T-and B-cell reactions with the production of antibodies against self-antigens [1,2,3,4]. Genetic, environmental, and hormonal factors play important roles in disease susceptibility [5]. Genetic variations in the genes involved in immune functions contribute to the development of autoimmune disorders [1]. Thus, immune receptor genes such as fragment crystallizable (Fc) receptor (FcR) and programmed cell death 1 (PDCD1) have always been candidate genes in polymorphism studies [6, 7].

FcRs on the leukocytes bind to the FC region of antibodies and enhance some functions, including phagocytosis of antibody-antigen complexes and generation of signals regulating cell activities [8]. Fc gamma receptor (FCγR) plays an important role in phagocytosis of antigens opsonized with complement component. Based on its hybrid desire, it is divided into three groups (FcγRI or CD64, FcγRII or CD32, and FcγRIII or CD16), which each of them exerts different functions [9, 10]. The genes coding FcγRII (CD32) and FcγRIII (CD16) are located on chromosome 1q23.3 [11]. Several genome-wide screens have shown that single nucleotide polymorphism (SNP) as a genetic variation can impair and/or change the normal functions of FcγRs and thereby results in the development of autoimmunity such as rheumatoid arthritis and SLE [12]. Some reports have indicated that SLE patients suffered from the reduced expressions of FcγRII and FcγRIII [13]. Furthermore, it is reported that the reduced expression of FcγRIIIA has a protective effect on lupus-susceptible mice through inhibiting the progression of lupus nephritis [14]. FcγRIIB, unlike FcγRIIC and FcγRIIA, exerts immunosuppressive impacts on some immune cells such as monocytes and B cells. FcγRIIB binding to its ligand (FC region of IgG) produces an inhibitory signal leading to a reduction in cell activation [15]. Genetic variation in FcγRII gene may contribute to SLE susceptibility in some populations [16]. Until now, several studies have been performed to clarify possible effects of FcγR polymorphisms, especially type IIA, IIB, and IIIA, on susceptibility to autoimmune diseases in different populations. Some reports have revealed that these SNPs play indispensible roles in disease susceptibility and sickness period in autoimmune disorders such as SLE [17,18,19,20,21].

Regarding the fact that FcγR polymorphisms act as genetic risk factor in developing autoimmunity [22] and their roles in SLE development have not yet been identified in the Iranian population, this study was aimed to determine whether two SNPs (rs1050501 and rs396991) in FcγRIIB and IIIA genes may associate with systemic lupus erythematosus disease activity index (SLEDAI) in the Iranian population.

Main text

Methods

Study samples

The study populations comprised of 80 unrelated SLE patients and 95 sex-and age-matched healthy individuals without history of autoimmune disorders and cancers (Additional file 1: Table S1). The patients approved for SLE disease by the specialist based on the SLE American College of Rheumatology (ACR) classification criteria [23]. Patients were interviewed by the specialist and disease activity index (DAI) was provided by a questionnaire according to SLEDAI-2K (30 days) guideline. The questionnaire contained 24 items, including seizure, psychosis, organic brain syndrome, visual disturbance, cranial nerve disorder, lupus headache, cerebrovascular accident (CVA), vasculitis, arthritis, myositis, urinary casts, hematuria, proteinuria, pyuria, rash, alopecia, mucosal ulcer, pleurisy, pericarditis, low complement, increased DNA binding, fever, thrombocytopenia, and leukopenia. There were eight scores (range: 0 to 8) for answering each item depending on symptom severities. Patients with more than 6 score were considered active. The researchers were blinded to patient information and contributed to this study without any costs. Participants were Persian ethnic and chosen from Isfahan province of Iran. The study was confirmed by the Ethics Committee of Isfahan University of Medical Sciences (ethic code: Ir.mui.rct.1396.3.668) and carried out based on the Helsinki declaration. Written informed consent was obtained from all subjects before entering the study.

Assessment of SNPs in extracted DNA

EDTA-treated blood samples (5 ml) were collected from participants. Genomic DNA was extracted from the leukocytes using a QIAamp DNA Mini kit (Qia gene, Germany) according to the manufacturer’s instructions. The yield and purity of DNAs were determined by nano drop (BioTek, Epoch, USA) and quality of DNAs were evaluated by electrophoresis gel. Afterwards, two SNPs were investigated by real-time polymerase chain reaction with high resolution melting (real-time PCR-HRM) analysis. Each reaction for FcγIIB and IIIA SNPs were carried out in a 10 μl mixture (Additional file 2: Table S2). Real-time PCR-HRM was done using Rotor Gene 6000 machine (Qiagen, Hilden, Germany). The machine was programmed as described previously [24]. To determine SNPs, the melting curves were analyzed in the temperature range of 65 °C to 95 °C at the end of each run. All reactions were carried out in duplicate. Primer sequences were indicated in Additional file 3: Table S3.

Statistical analysis

Data were analyzed using SPSS (v18; SPSS Inc. Chicago, IL, USA). Chi‐square and Fisher's exact tests were used to evaluate the associations of genotype and allele frequencies with SLE susceptibility and SLEDAI. Bonferroni correction, as a post hoc analysis, was used to the pairwise comparisons with significance level of 0.017. P-value < 0.05 was statistically considered significant.

Results

Description of patients

In this study, the most frequent clinical manifestations among 80 SLE patients were rash, arthritis, and leucopenia, while the most common laboratory manifestations were anti-nuclear antibodies (100%), anti-ds DNA (97.5%) and low complement (83.75%). The clinical and laboratory characteristics of patients with SLE are shown in Table 1.

Table 1 The clinical and laboratory characteristics of patients with SLE
Full size table

Associations of genotype and allele frequencies of FcγRIIB and FcγRIIIA with SLE susceptibility

Our data revealed that there were no significant differences in FcγRIIB genotype frequencies between patient and control groups (Table 2). Allelic analysis indicated that C and T allele frequencies of FcγRIIB in patients did not significantly differ from those of control group (Table 2).

Table 2 The genotypes and allele frequencies of FcγRIIB (rs1050501) and FcγRIIIA (rs396991) SNPs in patient and control groups
Full size table

In addition, statistical analyses indicated that FcγRIIIA genotype frequencies were not significantly different from those of healthy individuals (Table 2). As shown in Table 2, no significant differences were observed in T and G allele frequencies between patient and control groups. Other results indicated that T allele was the most frequent allele of FcγRIIIA SNP (Table 2).

Correlations of FcγRIIB and FcγRIIIA with SLEDAI

To determine the associations of FcγRIIB and FcγRIIIA with SLEDAI, the relationships of genotype and allele frequencies of these SNPs with some clinical parameters, which were the most frequent clinical manifestations of SLE patients, were evaluated. Our data indicated that genotype and allele frequencies of FcγRIIB were significantly associated with the incidences of leucopenia, rash, mucosal ulcer, arthritis, thrombocytopenia in SLE patients (P < 0.001–0.05, Table 3). The results of multiple comparisons revealed that there were significant correlations between distribution frequencies of FcγRIIB CC, CT and TT genotypes versus (vs) other genotypes and these clinical characteristics used to determine SLEDAI (P < 0.001–0.05, Table 3).

Table 3 The correlations of rs1050501 and rs396991 with some clinical manifestations used to SLEDAI
Full size table

Furthermore, other results of statistical analyses showed that the frequencies of some genotype and allele of FcγRIIIA played significant roles in determining SLEDAI. Similar to FcγRIIB, our results indicated that some genotype and allele frequencies of FcγRIIIA were significantly correlated to SLEDAI (P < 0.001–0.05, Table 5). The frequencies of FcγRIIIA TT, TG and GG genotypes vs other genotypes were significantly associated with SLEDAI (P < 0.001–0.05, Table 3).

Discussion

Numerous investigations stated that defects in genes related to the immune system can participate in the pathogenesis of autoimmune diseases such as SLE, but the roles of genetic agents have not clearly reported so far [25]. Thus, this study investigated rs1050501 and rs396991 SNPs and their associations with SLEDAI in an Iranian population from Isfahan province.

FcγRs have key roles in the immune system through regulating antibody effector functions. FcγRIIB expresses on different immune cells such as macrophages, B cells, granulocytes, and dendritic cells (DCs) [26]. This receptor suppresses the stimulation of B cells and reduces the development of autoimmunity. Some reports have shown that FcγRIIB SNP results in an amino acid substitution of threonine for isoleucine at position 232 (T232I), leading to decreased suppressor activities and thereby enhances susceptibility to SLE [27].

In this case–control study, genotype frequencies of FcγRIIB SNP showed that TT genotype frequency was higher in patient than healthy group, although the difference was not statistically significant. In agreement with this finding, Jeon et al. reported that a tendency for increase of TT genotype in SLE patients compared with healthy individuals, however, no significant difference was observed in this genotype between patient and healthy groups [9]. This finding proposes a key question why there is an inconsistency between TT genotype and T allele frequency in patients with SLE. As mentioned previous, T allele frequency showed a reduction in patients compared with healthy subjects. Despite a tendency for increase of CC genotype in SLE patients, the differences in CC and CT genotype frequencies between patient and healthy groups were not statistically significant. The increased frequency of CC genotype in patients was consistent with the tendency for increase of C allele number. Our data revealed that although there were some changes in the frequencies of genotypes and alleles between SLE patients and healthy subjects, these differences were not statistically considerable and rs1050501 was not associated with SLE susceptibility. In contrast with these observations, Zhu et al. in a meta-analysis study concluded that C allele of rs1050501 could be effective in SLE susceptibility and disease progression [28]. Furthermore, another study conducted by Pan et al. on 119 SLE patients from 95 nuclear families has indicated that C and T alleles of FcγRIIB were significantly associated with SLE and CT genotype was the most frequent genotype of FcγRIIB in SLE patients [29]. Although rs1050501 failed to show impact on SLE susceptibility in our study population, other statistical analyses indicated that genotype and allele frequencies of FcγRIIB could be considered as genetic factors to clarify SLEDAI in Iranian SLE patients. We observed that the frequencies of FcγRIIB genotypes and alleles were significantly correlated to some clinical parameters used to determine SLEDAI. Similar to this finding, a published short report manifested that the polymorphism of homozygous FcγRIIB-I232 was dramatically related to the elevated SLEDAI score [30]. Another study on other genotypes and alleles of FcγRIIB in an Indian population has revealed that the T allele was correlated to severity and clinical parameters of SLE [18].

FcγRIIIA gene is located on chromosome 1q23.3 and encodes for FcγRIIIA, a glycosylated heterogeneous form of FcγR [31, 32]. This receptor binds to immune complexes with low tendency and interestingly interacts with IgG2 subclass [33, 34]. It is stated that differences in genotypes and alleles of FcγRIIIA may be associated with autoimmunity [35]. Other results of this study indicated that GG genotype of rs396991 polymorphism had higher frequency in patients than healthy subjects. However, this difference was not statistically significant. On the contrary, TT, GT genotype frequencies were lower in patients than control group. These findings were agreed with the increased frequency of T allele in healthy subjects compared with SLE patients. Our data demonstrated that the frequency of G allele was in contrast with GG genotype frequency of FcγRIIIA SNP. Similar to the data of FcγRIIB SNP, allele and genotype frequencies of FcγRIIIA SNP in patients were not significant different from those of control group. These observations are consistent with the results of a study conducted on SLE patients showing the differences in genotypes and alleles of FcγRIIIA SNP between SLE and healthy subjects were not statistically significant [36]. Alansari et al. conducted a study on five SNPs in FcγR gene in three ethnic groups of SLE patients. The authors reported that genotype and allele frequencies of five SNPs in patients with SLE did not statistically differ from those of healthy subjects and subsequently concluded FcγR SNPs could not contribute to SLE susceptibility [37]. However, there are some studies revealing FcγRIIB and FcγRIIIA SNPs may participate in SLE development [38]. It is shown that 232TT genotype had an increased frequency in SLE patients compared with healthy subjects [39]. Dhaouadi et al. stated significant differences in allele and genotype frequencies of FcγRIIIA SNP between SLE and normal subjects in a Tunisian population [40]. In addition, other studies have reported that the decreased expression of FcγRIIIA contributed to SLE severity, but no significant relationship was observed between FcγRIIIA expression level and SLEDAI (38). In contrast, we found that the frequencies of some genotypes and alleles of FcγRIIIA were significantly associated with SLEDAI. This discrepancy may attribute to ethnic and geographic differences, inter-study heterogeneity in the studied SNPs and alleles, and sample size used in different studies.

Overall, although the current study failed to show the impacts of FcγRIIB and FcγRIIIA SNPs on SLE susceptibility, our data for the first time indicate that FcγRIIB and FcγRIIIA SNPs are associated with SLEDAI in the Iranian population.

Limitation

It should be noted that sample size may be a limitation of the study which may correlate to no correlations of these SNPs with SLE susceptibility. Therefore, more robust studies in different populations with larger sample size are needed to support our data and determine the effects of other FcγR SNPs in SLE development.

Availability of data and materials

The datasets generated and/or analysed during the current study are available in the ClinVar repository, Accession Numbers VCV000005467.1–VCV000225994.2.

Change history

Abbreviations

SLE:

Systemic lupus erythematosus

SNPs:

Single nucleotide polymorphisms

SLEDAI:

Systemic lupus erythematous disease activity index

FcγR:

Fragment crystallizable (Fc) receptor

PDCD1:

Programmed cell death 1

ACR:

American College of Rheumatology

CVA:

Cerebrovascular accident

DC:

Dendritic cell

References

  1. Fathi F, Sadeghi E, Lotfi N, Hafezi H, Ahmadi M, Mozafarpoor S, et al. Effects of the programmed cell death 1 (PDCD1) polymorphisms in susceptibility to systemic lupus erythematosus. Int J Immunogenet. 2020;47(1):57–64.

    Article  CAS  PubMed  Google Scholar 

  2. Fathi F, Atapour A, Eskandari N, Keyhanmehr N, Hafezi H, Mohammadi S, et al. Regulatory T-cells and their impacts on cytokine profile of end-stage renal disease patients suffering from systemic lupus erythematosus. Int J Immunopathol Pharmacol. 2019;33:2058738419863238.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Zhang Q, Liang Y, Yuan H, Li S, Wang J-B, Li X-M, et al. Integrated analysis of lncRNA, miRNA and mRNA expression profiling in patients with systemic lupus erythematosus. Arch Med Sci. 2019;15(4):872.

    Article  CAS  PubMed  Google Scholar 

  4. Tao C-Y, Shang J, Chen T, Yu D, Jiang Y-M, Liu D, et al. Impact of antimalarial (AM) on serum lipids in systemic lupus erythematosus (SLE) patients: a systematic review and meta-analysis. Medicine. 2019;98:14.

    Google Scholar 

  5. Yang J, Zhu J-M, Wu S, Li J, Wang M-R, Wang T-T, et al. Association study between the TP53 Rs1042522G/C polymorphism and susceptibility to systemic lupus erythematosus in a Chinese Han population. Rheumatol Int. 2017;37(4):523–9.

    Article  CAS  PubMed  Google Scholar 

  6. Fathi F, Ebrahimi M, Eslami A, Hafezi H, Eskandari N, Motedayyen H. Association of programmed death-1 gene polymorphisms with the risk of basal cell carcinoma. Int J Immunogenet. 2019;46(6):444–50.

    Article  CAS  PubMed  Google Scholar 

  7. Fathi F, Zamani B, Piroozmand A, Mozafarpoor S, Seyedhashemi E, ArefNezhad R, et al. Programmed cell death 1 (PDCD1) gene haplotypes and susceptibility of patients to basal cell carcinoma. Mol Biol Rep. 2021;8:1–7.

    Google Scholar 

  8. Lichtman AH, Abbas AK, Pillai S. Immunologia cellulare e molecolare: Elsevier Italia; 2015.

  9. Jeon J-Y, Kim K-Y, Kim B-S, Jung J-Y, Kim H-A, Suh C-H. FcγRIIB gene polymorphisms are associated with disease risk and clinical manifestations of systemic lupus erythematosus in Koreans. Tohoku J Exp Med. 2015;236(3):185–91.

    Article  CAS  PubMed  Google Scholar 

  10. Werwitzke S, Trick D, Sondermann P, Kamino K, Schlegelberger B, Kniesch K, et al. Treatment of lupus-prone NZB/NZW F1 mice with recombinant soluble Fcγ receptor II (CD32). Ann Rheum Dis. 2008;67(2):154–61.

    Article  CAS  PubMed  Google Scholar 

  11. Tsang-A-Sjoe MW, Nagelkerke SQ, Bultink IE, Geissler J, Tanck MW, Tacke CE, et al. Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis. Rheumatology. 2016;55(5):939–48.

    Article  CAS  PubMed  Google Scholar 

  12. van Velde NC, Mottram PL, Hogarth PM. FcγRII and multi-system autoimmune disease. New York: Springer; 2006.

    Book  Google Scholar 

  13. Szücs G, Kavai M, Kiss E, Csipö I, Szegedi G. Correlation of IgG Fc receptors on granulocytes with serum immune complex level in systemic lupus erythematosus. Scand J Immunol. 1995;42(5):577–80.

    Article  PubMed  Google Scholar 

  14. Hepburn A, Mason J, Davies K. Expression of Fcγ and complement receptors on peripheral blood monocytes in systemic lupus erythematosus and rheumatoid arthritis. Rheumatology. 2004;43(5):547–54.

    Article  CAS  PubMed  Google Scholar 

  15. Yu X, Lazarus AH. Targeting FcγRs to treat antibody-dependent autoimmunity. Autoimmun Rev. 2016;15(6):510–2.

    Article  CAS  PubMed  Google Scholar 

  16. Zuñiga R, Ng S, Peterson MG, Reveille JD, Baethge BA, Alarcón GS, et al. Low-binding alleles of Fcγ receptor types IIA and IIIA are inherited independently and are associated with systemic lupus erythematosus in Hispanic patients. Arthrit Rheum. 2001;44(2):361–7.

    Article  Google Scholar 

  17. Tsao B. Genetic susceptibility to lupus nephritis. Lupus. 1998;7(9):585–90.

    Article  CAS  PubMed  Google Scholar 

  18. Pradhan V, Patwardhan M, Nadkarni A, Ghosh K. Fc γ R IIB gene polymorphisms in Indian systemic lupus erythematosus (SLE) patients. Indian J Med Res. 2011;134(2):181.

    CAS  PubMed  PubMed Central  Google Scholar 

  19. Nimmerjahn F, Ravetch JV. Fcγ receptors as regulators of immune responses. Nat Rev Immunol. 2008;8(1):34–47.

    Article  CAS  PubMed  Google Scholar 

  20. Bombardier C, Gladman DD, Urowitz MB, Caron D, Chang CH, Austin A, et al. Derivation of the SLEDAI. A disease activity index for lupus patients. Arthrit Rheumat. 1992;35(6):630–40.

    Article  CAS  Google Scholar 

  21. Manger K, Repp R, Jansen M, Geisselbrecht M, Wassmuth R, Westerdaal N, et al. Fcγ receptor IIa, IIIa, and IIIb polymorphisms in German patients with systemic lupus erythematosus: association with clinical symptoms. Ann Rheum Dis. 2002;61(9):786–92.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Takai T. Roles of Fc receptors in autoimmunity. Nat Rev Immunol. 2002;2(8):580–92.

    Article  CAS  PubMed  Google Scholar 

  23. Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthrit Rheum. 1997;40(9):1725.

    Article  CAS  Google Scholar 

  24. Taheri RA, Motedayyen H, Ghotloo S, Masjedi M, Mosaffa N, Mirshafiey A, et al. The effect of lipopolysaccharide on the expression level of immunomodulatory and immunostimulatory factors of human amniotic epithelial cells. BMC Res Notes. 2018;11(1):1–5.

    Article  Google Scholar 

  25. da Cruz HLA, Cavalcanti CAJ, de Azêvedo SJ, de Lima CAD, Fragoso TS, Barbosa AD, et al. Differential expression of the inflammasome complex genes in systemic lupus erythematosus. Immunogenetics. 2020;89:1–8.

    Google Scholar 

  26. Morris AB, Farley CR, Pinelli DF, Adams LE, Cragg MS, Boss JM, et al. Signaling through the inhibitory Fc receptor FcγRIIB induces CD8+ T cell apoptosis to limit T cell immunity. Immunity. 2020;52(1):136–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Espéli M, Bashford-Rogers R, Sowerby JM, Alouche N, Wong L, Denton AE, et al. FcγRIIb differentially regulates pre-immune and germinal center B cell tolerance in mouse and human. Nat Commun. 2019;10(1):1–14.

    Article  Google Scholar 

  28. Zhu X-W, Wang Y, Wei Y-H, Zhao P-P, Wang X-B, Rong J-J, et al. Comprehensive Assessment of the Association between FCGR s polymorphisms and the risk of systemic lupus erythematosus: Evidence from a Meta-Analysis. Sci Rep. 2016;6(1):1–13.

    Article  Google Scholar 

  29. Pan F, Zhang K, Li X, Xu J, Hao J, Ye D. Association of Fcγ receptor IIB gene polymorphism with genetic susceptibility to systemic lupus erythematosus in Chinese populations—A family-based association study. J Dermatol Sci. 2006;43(1):35–41.

    Article  CAS  PubMed  Google Scholar 

  30. Hu W, Zhang Y, Sun X, Zhang T, Xu L, Xie H, et al. FcγRIIB-I232T polymorphic change allosterically suppresses ligand binding. Elife. 2019;8:e46689.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Hollox EJ, Detering JC, Dehnugara T. An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus. Hum Mutat. 2009;30(3):477–84.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Liu B, Maier LA, Hamzeh N, MacPhail K, Mroz MM, Liu H, et al. Polymorphism of FCGR3A gene in chronic beryllium disease. Genes Immun. 2019;20(6):493–9.

    Article  CAS  PubMed  Google Scholar 

  33. Niwa R, Natsume A, Uehara A, Wakitani M, Iida S, Uchida K, et al. IgG subclass-independent improvement of antibody-dependent cellular cytotoxicity by fucose removal from Asn297-linked oligosaccharides. J Immunol Methods. 2005;306(1–2):151–60.

    Article  CAS  PubMed  Google Scholar 

  34. Grecco M, Santos VC, Pereira KMC, Andrade LEC, Silva NP. Fc gamma receptor IIIa polymorphism is not associated with susceptibility to systemic lupus erythematosus in Brazilian patients. Revista Brasi Reumatol. 2016;56(6):515–20.

    Article  Google Scholar 

  35. González-Escribano M, Aguilar F, Sánchez-Román J, Núñez-Roldán A. FcgRIIA, FcγRIIIA and FcγRIIIB polymorphisms in Spanish patients with systemic lupus erythematosus. Eur J Immunogenet. 2002;29(4):301–6.

    Article  PubMed  Google Scholar 

  36. Yap S, Phipps M, Manivasagar M, Tan S, Bosco J. Human Fc gamma receptor IIA (FcγRIIA) genotyping and association with systemic lupus erythematosus (SLE) in Chinese and Malays in Malaysia. Lupus. 1999;8(4):305–10.

    Article  CAS  PubMed  Google Scholar 

  37. Alansari A, Gul A, Inanc M, Ordi J, Teh L-S, Ollier WE, et al. Fc receptor gamma subunit polymorphisms and systemic lupus erythematosus. Saudi Med J. 2004;25(10):1445–8.

    PubMed  Google Scholar 

  38. Zhou M, Li L-H, Peng H, Li R, Feng C-C, Xu W-D, et al. Decreased ITGAM and FcγRIIIA mRNA expression levels in peripheral blood mononuclear cells from patients with systemic lupus erythematosus. Clin Exp Med. 2014;14(3):269–74.

    Article  CAS  PubMed  Google Scholar 

  39. Kyogoku C, Dijstelbloem HM, Tsuchiya N, Hatta Y, Kato H, Yamaguchi A, et al. Fcγ receptor gene polymorphisms in Japanese patients with systemic lupus erythematosus: contribution of FCGR2B to genetic susceptibility. Arthritis Rheum. 2002;46(5):1242–54.

    Article  CAS  PubMed  Google Scholar 

  40. Dhaouadi T, Sfar I, Hassine LB, Turki S, Khalfallah N, Ben T. PTPN22, CTLA4, FcγRIIa, FcγRIIIa and FcγRIIIb polymorphisms in Tunisian patients with systemic lupus erythematosus. Int J Clin Rheumatol. 2019;14(1):9.

    Article  Google Scholar 

Download references

Acknowledgements

The authors thank all subjects who participated in the study.

Funding

This study was supported by Isfahan University of Medical Sciences (Grant No: 396668).

Author information

Authors and Affiliations

  1. Department of Rheumatology, Alzahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran

    Mansoor Karimifar & Khosro Akbari

  2. Department of Anatomy, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

    Reza ArefNezhad

  3. Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

    Farshid Fathi

  4. Ariagene Medical Genetic Laboratory, Isfahan, Iran

    Mohammad Mousaei Ghasroldasht

  5. Department of Obstetrics and Gynecology, University of Chicago, 5841 S. Maryland Ave., Chicago, IL, 60637, USA

    Mohammad Mousaei Ghasroldasht

  6. Autoimmune Diseases Research Center, Shahid Beheshti Hospital, Kashan University of Medical Sciences, 5th Kilometer of Ravand Road, Kashan, Iran

    Hossein Motedayyen

Authors
  1. Mansoor Karimifar
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Khosro Akbari
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Reza ArefNezhad
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Farshid Fathi
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Mohammad Mousaei Ghasroldasht
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Hossein Motedayyen
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

MK and KHA participated in the disease diagnosis, sample collections, and obtained funding for the work. FF and RA participated in the design of some experiments and statistical analysis of the data. MMG carried out some of the experiments. HM participated in the study design and drafted the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Hossein Motedayyen.

Ethics declarations

Ethics approval and consent to participate

This work was confirmed by the Ethics Committee of Isfahan University of Medical Sciences (ethic code: Ir.mui.rct.1396.3.668). Written informed consent to participate in the study was obtained from all subjects before entering the study.

Consent for publication

Not applicable. Consent to publish the data was obtained from participants prior to entering the study.

Competing interests

The authors have no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

The original online version of this article was revised to replace an incorrect author name with that of the correct author.

Supplementary Information

Additional file 1.

Table. S1) Demographic characteristics of participants.

Additional file 2.

Table S2) Components and their volumes used to PCR-HRM.

Additional file 3.

Table. S3) Primer sequences used to PCR-HRM.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Karimifar, M., Akbari, K., ArefNezhad, R. et al. Impacts of FcγRIIB and FcγRIIIA gene polymorphisms on systemic lupus erythematous disease activity index. BMC Res Notes 14, 455 (2021). https://0-doi-org.brum.beds.ac.uk/10.1186/s13104-021-05868-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s13104-021-05868-2

Keywords

BMC Research Notes

ISSN: 1756-0500

Contact us