Association study between KIR polymorphisms and rheumatoid arthritis disease: an updated meta-analysis

Rheumatoid arthritis (RA) is a common chronic autoinflammatory disorder, which is characterized by erosive articular lesions and progressive joint destruction, resulting in irreversible bone deformity and movement disabilities [1, 2]. The overall prevalence of RA ranges from 0.5 to 1% in global populations [3]. It predominantly affects women with a female to male ratio of 2:1. It is believed that the combination of genetic and environmental factors as well as epigenomic contributing factors can break the self-tolerance and provoke immune system against itself during autoimmunity [4‐8]. Current studies have reported approximately 60% genetic contribution in susceptibility to RA in various ethnic populations [9‐11]. Human leukocyte antigen (HLA)-DR, one of the histocompatibility genes in HLA class II region, is responsible for about 30% of genetic susceptibility to RA [12]. Thus, several genes outside the HLA region are also pivotal for initiation and development of RA. As shown in previous studies, a number of genes, including PTPN22, PADI4, STAT4, TRAF1, TNFAIP3, CD40, and KIR have been associated with RA and drawn much attention to investigate more genetic elements contributing to RA risk [9, 13‐17].

The essential role of natural killer (NK) cells in RA pathogenesis have been widely investigated in many studies. These cells are present in synovial fluid as well as the blood of RA patients and participate in inflammation and, therefore, damage of joints [18, 19]. In normal physiological conditions, NK cells are able to eliminate target cells with little or no expression of HLA class I molecules on them. Beside cytotoxic function, their ability to secrete cytokines underlines the role of NK cells in development of autoimmune settings [20]. The efficient functional activity of NK cells is governed by three distinct receptor families including, C-type lectin-like group, immunoglobulin (Ig)-like superfamily, and natural cytotoxicity receptors (NCR) [21]. The KIRs (CD 158 family) are expressed mainly on NK cells and a few proportions of T lymphocytes. HLA class I molecules are considered to be the major ligands for KIRs [22]. The cluster of KIR genes is mapped on the leukocyte receptor complex (LRC) locus on chromosome 19q13.4 which is extremely polymorphic among individuals and codes for glycoprotein receptors acting in inhibitory and activating manner [23]. In humans, 17 highly homologous genes have been recognized for KIR genes encoding receptors containing 9 inhibitory, 6 activating, and 2 pseudogenes [24, 25]. KIR receptors are categorized based on the number of their extracellular Ig-like domains (2D or 3D) and whether they have short (S) or long (L) cytoplasmic tail. Two pseudogenes (2DP1 and 3DP1) do not encode functional receptors [26]. Inhibitory KIRs contain long intracellular tails and transduce signals through immunoreceptor tyrosine-based inhibitory motifs (ITIM). On the other hand, activating signals are generated through stimulation of a transmembrane adaptor molecule, namely DNAX activation protein of 12 kDa (DAP12), which possess domains for immunoreceptor tyrosine-based activating motifs (ITAM) [27, 28].

The association of KIR gene polymorphisms has already been demonstrated in several autoimmune disorders [29, 30]. Previously, 11 genetic studies have tried to clarify the role of KIR polymorphisms in susceptibility to RA. Nonetheless, findings from these studies seem to be contradictory in some cases. This discrepancy may be due to small sample sizes, insufficient statistical power and ethnic variations among different populations. Meta-analysis is a statistical method that combines data from multiple researches to establish a reliable estimation. Therefore, in this meta-analysis, we intend to provide a comprehensive evaluation of previously published studies about KIR association with RA susceptibility to have a conclusive and consistent understanding of the role of these molecules in RA pathogenesis.

We intend to perform this meta-analysis to achieve a comprehensive analysis of the previously published studies about KIR association with RA susceptibility to figure out a conclusive and consistent understanding of the RA pathogenesis underlying KIR gene polymorphisms. The analysis revealed significant association of 2DL3, 2DL5, 2DS5, and 3DL3 genes, which decreased RA risk.

RA is a common autoimmune disorder, which mainly affects the joints and brings about bone erosions. One subject of debate at present is the role of genetic elements, which are involved in the initiation and development of RA. Integration analysis of genome wide association study (GWAS) successfully reported newly natural killer cell mediated cytotoxicity pathway as a contributing genes which are associated with RA [42].

Human NK cells are CD3⁻CD56⁺ lymphocytes of innate immune system and are subdivided into CD56^bright and CD56^dim phenotypes based on CD56 expression level. While CD56^dim NK cells participate in cytotoxic responses, CD56^bright subsets are highly involved in cytokine secretion especially interferon (IFN)-γ. According to previous researches, following diminished frequency of NK cells in peripheral blood, CD56^bright subsets could migrate through blood vessels to inflamed joints and propagated in the synovial fluid of RA patients [43, 44]. Enhancement of NK cells in synovial fluids resulted in high amount of IFN-γ production which, in turn, contributed to perpetuation of inflammatory milieu in this autoimmune disorder [45]. Of note, IFN-γ per se has ability to activate surrounding macrophages through cell-cell contact to release more inflammatory mediators, mostly tumor necrosis factor (TNF)-α which reinforce inflammatory environment in arthritic joints [46].

NK cells are also responsible for killing target cells that are not able to express self-MHC molecules [47]. Their function is highly modulated by several activating and inhibitory membrane receptors, particularly KIRs [26]. In 2001, the first case-control research regarding association of KIRs and RA undertaken by Yen et al. that showed the KIR2DS2 involvement in the development of rheumatoid vasculitis [33]. From 2001 up to now, several studies were carried out to delineate the relationship of KIR genes repertoire with susceptibility to RA in diverse ethnic populations, though the findings appear inconsistent and conflicting. Thus, we decided to fulfill this comprehensive meta-analysis by incorporating data of 11 relevant studies in order to reevaluate the interest associations. The overall results divulged that KIR2DL3, KIR2DL5, KIR3DL3, and KIR2DS5 were negatively associated with susceptibility to RA, providing evidence that KIRs might potentially affect RA progression. On the other hand, other KIR genes, including 2DL1, 2DL2, 2DL4, 3DL1, 3DL2, 3DS1, 2DS1-2DS4, and two pseudo gens of 2DP1 and 3DP1 displayed no significant association with RA risk in our study.

KIR genes consist of two haplotypes; The “A” haplotype contains inhibitory genes and one activating gene (KIR2DS4) with protective effect against autoimmunities. “B” haplotype, on the other hand, exhibits more activating gens (KIR2DS1, -2DS2, -2DS3, -2DS4, -2DS5, and -3DS1) and inhibitory genes, KIR2DL2 and KIR2DL5 that increase the risk of autoimmune disorders [24, 26, 48]. It is widely accepted that the proper activation of NK cells depends on the equilibrium of activating and inhibitory KIR receptors. Considering their high degree of polymorphisms in two levels of gene content and allelic variations, they are mostly related to many autoimmune diseases, such as RA, ankylosing spondylitis, psoriasis vulgaris, scleroderma, SLE, diabetes mellitus, Crohn’s disease, Behçet’s disease, and etc. [21, 39, 49‐54].

In this study, KIR2DL3 showed negative association with the RA risk and in agreement with the results of Parkash et al. and Ramirez-De los Santos et al. studies, it provided protection against RA [12, 38]. In this context, it has been clarified earlier that KIR2DL3 inhibits the production of cytokines like IFN-γ. Of note, NK cells-derived IFN-γ is a fundamental source for Th1 priming in RA [55]. Therefore, lack of IFN-γ secretion by NK cells could reduce T cells autoreactivity [56].

In addition, our results also suggest that KIR2DL5 and KIR2DS5 were protective against RA. KIR2DL5 and KIR2DS5 both are present at haplotype B, but they function differently in the inhibitory and activating manner, respectively. Meanwhile, their respective ligands have not been discovered successfully [57].

Interestingly, KIR2DS5 display protective effect in some diseases, despite an activating function. A study by Nowak et al. showed that KIR2DS5 plays a protective role in ankylosing spondylitis, endometriosis, and acute kidney graft rejection with no significant effect in RA. According to their literature, this paradoxical protective effect is likely related to the pronounced role of KIR2DS5 in tolerance induction and, therefore, prevention of autoimmune conditions [37]. It should be noted that this phenomenon might be due to linkage disequilibrium (LD) with some neighboring inhibitory loci in KIR haplotype. Thus, LD can contribute to modulate gene expression and give explanation as a putative cause of protective effect of KIR2DS5.

It has been reported previously that KIR2DL5 significantly had protective effect in SLE patients. Due to inhibitory signals from KIR2DL5, NK cells functions can be suppressed in the onset of SLE. Moreover, the less prevalence of KIR2DL5 associated with the increased predisposition to overall infections in SLE patients [58]. Although their findings could not support the relation of KIR2DL5 in RA individuals, we observed a highly significant association of KIR2DL5 with risk of RA in our population study, which may impress the disease susceptibility in the same manner as does in SLE.

KIR3DL3 is one of the so-called “framework” genes, which is present in all KIR haplotypes. It is located in the centromeric half of haplotype at 5’-end and its ligand is uncertain yet [59]. This inhibitory receptor can prohibit NK cell cytotoxicity via single ITIM motif in its cytoplasmic tail. Unlike previous reports, we revealed that a negative association exist between KIR3DL3 and RA risk.

A meta-analysis undertaken by Li et al. in 2015 to evaluate association between KIR variations and RA risk in East Asians and Caucasians subpopulations. The findings of their survey represented two positive associations, including 2DL1, 2DS1, and 2DL3 as a protective factor for RA risk only in East Asians, but not in Caucasians [60]. In the current study, we incorporated more studies with further ethnic populations to achieve better results. The only consistence results obtained from current meta-analysis and that of Li et al. study, was 2DL3 as protective factor in RA patients [60]. While the previous meta-analysis found two positive associations of KIR genes with RA susceptibility, we found that all significantly associated KIR genes had negative association with RA risk. KIR2DL5, KIR2DS5, and KIR3DL3 conferred a protective role in RA development [60].

This meta-analysis provides comprehensive information from 11 case-control studies to better understanding of KIR and RA association, but some shortcomings should be considered. First, between-study heterogeneity was observed which might distort analysis. Second, the number of published studies entered in this research was relatively small which restrict the estimation power of the present study. However, considering the increased number of subjects included in this meta-analysis, the obtained results are more reliable than the previous analysis [60]. Additionally, various populations of Europe, Asia, and American nations were included in the current meta-analysis, increasing the general conclusion of the results to populations worldwide.

In consideration of all, present meta-analysis identified that‌ KIR2DL3, KIR2DL5, KIR2DS5, and KIR3DL3 seem to have a potential protective role in RA risk. However, premised on forenamed limitations, further research studies are still required to explore the association between the KIR polymorphisms and RA risk with a larger sample sizes and controls in order to validate these findings.