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REVIEW article

Front. Immunol., 29 January 2013
Sec. NK and Innate Lymphoid Cell Biology
This article is part of the Research Topic Ligand specificity of Killer cell Immunoglobulin Receptors View all 7 articles

Killer Cell Immunoglobulin-Like Receptor Gene Associations with Autoimmune and Allergic Diseases, Recurrent Spontaneous Abortion, and Neoplasms

  • Laboratory of Immunogenetics and Tissue Immunology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland

Killer cell immunoglobulin-like receptors (KIRs) are a family of cell surface inhibitory or activating receptors expressed on natural killer cells and some subpopulations of T lymphocytes. KIR genes are clustered in the 19q13.4 region and are characterized by both allelic (high numbers of variants) and haplotypic (different numbers of genes for inhibitory and activating receptors on individual chromosomes) polymorphism. This contributes to diverse susceptibility to diseases and other clinical situations. Associations of KIR genes, as well as of genes for their ligands, with selected diseases such as psoriasis vulgaris and atopic dermatitis, rheumatoid arthritis, recurrent spontaneous abortion, and non-small cell lung cancer are discussed in the context of NK and T cell functions.

Introduction

Killer cell immunoglobulin-like receptors (KIRs) are a family of cell surface receptors. KIR proteins possess two (KIR2D) or three (KIR3D) immunoglobulin-like domains in their extracellular region. KIRs are expressed on natural killer (NK) cells and some subpopulations of T lymphocytes, and therefore may influence the activation of both cell types. They do it either by inhibition of cell activation [inhibitory KIRs, with long (L) cytoplasmic tail – KIR2DL and KIR3DL – which contains immunoreceptor tyrosine-based inhibitory motifs, ITIMs], or by activation of a cell [activating KIRs, KIR2DS, and KIR3DS, with short (S) cytoplasmic tail having no signaling motifs but associated with adapter molecule, DAP12 homodimer, which possesses immunoreceptor tyrosine-based activating motifs, ITAMs]. Upon ligand binding by inhibitory KIR, tyrosine residues in its ITIMs become phosphorylated, which is recognized by a phosphatase, which then dephosphorylates proteins of the signaling pathway, phosphorylated previously due to cell activation. On the other hand, ligand binding by activating KIR results in tyrosine phosphorylation in ITAMs of DAP12 molecule, and this leads to activation of kinases of signaling pathway and cell activation. KIR ligands, where known, are HLA class I molecules (Table 1). All allomorphs of HLA-C are recognized by some inhibitory KIRs, whereas less than 50% of HLA-A and HLA-B allomorphs present in human populations are recognized by KIRs (Parham et al., 2012a). Differing in the amino acid residue in position 80, HLA-C allomorphs fall into two groups, C1 (Asn80) and C2 (Lys80), recognized by KIR2DL2/KIR2DL3 and KIR2DL1/KIR2DS1, respectively (Table 1). As a rule, when inhibitory and activating KIRs have the same or similar HLA specificity (such as KIR2DL1 and KIR2DS1), then binding of inhibitory KIR to its ligand is characterized by higher affinity than binding of activating KIR to the same ligand (Vales-Gomez et al., 1998). This protects normal cells of the body, displaying normal quantity of HLA class I molecules, against the NK cell attack (efficient inhibition), but ensures killing of virus-infected or malignant cells with low or none expression of one or all HLA class I alleles (non-efficient inhibition; “missing-self” theory, Ljunggren and Kärre, 1990).

TABLE 1
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Table 1. Ligands of KIR molecules (based on Kusnierczyk, 2006; Graef et al., 2009; Campbell and Purdy, 2011; Parham et al., 2012b; and references therein, modified).

KIR genes are clustered in the leukocyte receptor complex (LRC) of genes located in the 19q13.4 region and are characterized by both allelic (high numbers of variants) and haplotypic (different numbers of genes for inhibitory and activating receptors on individual chromosomes) polymorphism (Parham et al., 2012a). Some KIR genes (KIR3DL2, KIR3DL3, and KIR2DL4) are called “framework genes,” because they are present in all haplotypes. Other genes are present only in some of them, in multiple different combinations. Haplotypes consisting mostly of inhibitory genes (so called “A” haplotypes) tend to be associated with lower risk of autoimmune diseases, but higher risk of viral infections than haplotypes (“B” haplotypes) containing several activating KIR genes (see Parham, 2005; Khakoo and Carrington, 2006; Kusnierczyk, 2006; Boyton and Altmann, 2007; Campbell and Purdy, 2011)1.

Associations of KIR and their HLA ligand genes have been studied in multiple human diseases, and reviewing all of these here would not be possible. Therefore, selected clinical conditions, most familiar to my laboratory, are summarized and discussed below.

Skin Diseases: Psoriasis and Atopic Dermatitis

Psoriasis

Psoriasis is a multifactorial skin disease with autoimmune features, which are manifested by T lymphocyte infiltration to both dermis and epidermis (Lew et al., 2004) and by antipsoriatic activity of immunosuppressants such as recombinant soluble CTLA-4 (Sivamani et al., 2012). Although etiology of this disorder is still not definitely elucidated, it is known that both environmental and genetic factors are involved. Genome-wide association studies revealed at least 13 psoriasis susceptibility loci (PSORS1-13)2. Among these, the strongest linkage and association was reproducibly described for HLA-Cw*06 allele located on PSORS1 locus and encoding a ligand for KIR2DL1 and KIR2DS1 receptors (see text footnote 2). Several lines of evidence show contribution of NK or T lymphocytes expressing NK cell receptors, among them KIRs (Gilhar et al., 2002; Liao et al., 2006). Therefore, we examined whether inhibitory or activating KIR genes might be associated with susceptibility to psoriasis vulgaris, most common clinical form of this disease. We typed 114 and 116 patients for HLA-C alleles and KIR genes, respectively, and compared their frequencies with those in 123 unrelated healthy control individuals. We found, first, a strong association of psoriasis with HLA-Cw*06, which was strongest in individuals whose age at disease onset was up to 20 years, and decreased in patient groups with later age at onset (Luszczek et al., 2002). Not surprisingly, we found an association of KIR2DS1 gene, coding for an activating receptor recognizing HLA-Cw*06 (HLA-Cw*06 belongs to C2 group of HLA-C epitopes), with psoriasis vulgaris. However, in contrast to HLA-Cw*06, association of KIR2DS1 with psoriasis seemed stronger in higher age at onset values, although the age effect was not significant because of small numbers of patients with late disease onset (Luszczek et al., 2004). Very similar association of KIR2DS1 (and KIR2DL5 in addition, which was not analyzed in our study) was simultaneously published for Japanese population, genetically distant from Poles (Suzuki et al., 2004), and confirmed later in Swedish and Brazilian Caucasians with psoriasis vulgaris (Holm et al., 2005; Jobim et al., 2008), but not in Swedes with guttate psoriasis (Holm et al., 2005) or in Taiwanese Chinese with plaque psoriasis (Chang et al., 2006; see Table 2). Interestingly, KIR2DS1 gene appeared associated also with psoriatic arthritis (Martin et al., 2002b; Holm et al., 2005; Williams et al., 2005; Table 2). In this latter disease, both KIR2DS1 in the absence of C2, and KIR2DS2 in the absence of C1 group HLA-C alleles were observed associated with psoriatic arthritis (Martin et al., 2002b; Nelson et al., 2004) in addition to other genes (HLA-B*27 and HLA-Cw*0602), although in American population the effect of KIR2DS1 was independent from C2 presence (Williams et al., 2005).

TABLE 2
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Table 2. KIR2DS1 gene associations with clinical forms of psoriasis in different ethnic groups.

We observed also some effects of other KIR genes in psoriatic patients positive for KIR2DS1: namely, increased frequency of a deletion variant of KIR2DS4 and decreased frequency of KIR2DS3 and KIR2DS5 gene in comparison to KIR2DS1-positive controls (Ploski et al., 2006). A seemingly protective effect of KIR2DS5 gene presence was seen also in other diseases (Nowak et al., 2010). The deletion variant of KIR2DS4 gene (Hsu et al., 2002a,b; Maxwell et al., 2002, 2004) potentially encodes a soluble protein, although this has not been proven, and its transcription level is very low (McErlean et al., 2010).

In summary, KIR2DS1 gene seems to be a major factor in the LRC region contributing to the susceptibility to psoriasis vulgaris and related diseases which are also associated with a gene for its ligand, HLA-Cw*06.

Atopic Dermatitis

Atopic dermatitis (AD) is a chronic or relapsing inflammatory skin disorder of complex etiology, affecting up to 20% of children and often followed later by development of asthma and other allergic diseases. Multiple immunological disturbances were described. Disruption of epidermal barrier increases a susceptibility of AD patients to microbial infections, both bacterial (Staphylococcus aureus in most cases) and viral (localized or disseminated infections, most often by Herpes simplex virus; De Benedetto et al., 2009; Boguniewicz and Leung, 2011). As NK cells are among many cell types whose activity might be biased in AD, we were interested whether KIR and KIR ligand genotype of AD patients would differ from that of healthy persons. We compared KIR gene frequencies in a group of 240 patients diagnosed with AD with those in 690 healthy individuals representative for several regions of Poland. Distribution of KIR genes in both groups was very similar, with one exception: KIR2DS1 gene was present less frequently in patients than in controls. This latter observation was confirmed on the second cohort of 201 patients from a different region of Poland (Niepieklo-Miniewska et al., submitted).

The reason why KIR2DS1 gene has been found associated with psoriasis and psoriatic arthritis (see Psoriasis) but seemingly protective against another inflammatory skin disease, AD, is not clear. Psoriasis is believed to be a Th1-regulated disease, whereas Th2 response dominates in AD (Rabin and Levinson, 2008; von Bubnoff et al., 2010). This division is not so sharp in nature, however (Guttman-Yasky et al., 2011), although microarray analysis confirms it to a great extent (Nomura et al., 2003; Choy et al., 2012). Keratinocytes hyperproliferate in psoriasis but undergo apoptosis in AD (Albanesi et al., 2007; Kastelan et al., 2009; Rebane et al., 2012). Therefore, different KIR2DS1-positive cell subpopulations may contribute to both types of the disease, resulting in opposite associations of KIR2DS1 gene.

Rheumatoid Arthritis

Another disease, where KIR gene associations were examined, was rheumatoid arthritis (RA). This disorder is a chronic systemic inflammatory polyarthritis affecting about 1% of individuals in Caucasian populations, and T cells contribute to its pathomechanism (Jacob and Jacob, 2012). The involvement of NK cells in RA was also described (Dalbeth et al., 2004; Falgarone et al., 2005). RA is a multifactorial disease, and strongest genetic association was reproducibly shown for so called shared epitope of HLA-DR; however, it explains only one-third to a half of the genetically determined susceptibility to the disease (Bowes and Barton, 2008). The expression of KIR2DS2 molecule on T cells with unusual phenotype, CD4+CD28-KIR+, and an association of KIR2DS2 but not KIR2DS1 gene with vascular inflammatory complication of RA were described by Joerg Goronzy’s group (Yen et al., 2001). Other KIR genes were not tested by these authors. Therefore, we compared KIR gene frequencies in 177 RA patients and 243 control individuals. Although no differences between the whole group of patients and controls were found (Majorczyk et al., 2007) – similarly to simultaneously published study of Northern Irish RA patients (Middleton et al., 2007), nevertheless KIR2DS2 gene was associated with vasculitis also in our population of patients. In addition, frequency of KIR2DL2 gene, not tested by Yen et al. (2001), was also increased in vasculitis (Majorczyk et al., 2007). Both these genes are in very strong linkage disequilibrium in Caucasians, which makes differentiation between their effects impossible. However, increased frequency of CD4+CD28 T cell clones positive for KIR2DS2 but negative for KIR2DL2 gene expression, observed in RA vasculitis by Yen et al. (2001), speaks for the role of the former gene in this complication of RA. Interestingly, CD4+CD28 T cells described in RA vasculitis were found only in human cytomegalovirus-seropositive, but not in HCMV-negative RA patients, and their specificity was predominantly directed toward HCMV antigens. If they cross-react weakly with some autoantigens, then KIR2DS2 binding to yet unknown ligands might boost these T cells to autoaggression (van Bergen and Koning, 2010).

Furthermore, the frequencies of KIR2DS1 and KIR3DS1 were lower in our patients without bone erosions than in those with erosions and controls. Another interesting finding we made was that RA patients positive for KIR2DL3 and negative for KIR2DS3 had earlier disease diagnosis. On the other hand, we observed no associations of KIR genes with autoantibodies: rheumatoid factor or anti-cyclic citrullinated peptide (Majorczyk et al., 2007).

Thus, although a susceptibility to RA does not seem to be influenced by particular KIR genes, some clinical manifestations of this disease such as vasculitis, bone erosions, and age at onset, are associated with distinct KIR genes, which might reflect participation of different subpopulations of T and/or NK cells.

Immunogenetics of Reproduction

Recurrent Spontaneous Abortion

Spontaneous abortion is the most frequent disorder of human pregnancy. Approximately 10–15% of pregnancies end in miscarriage during the first trimester, and even many more spontaneous abortions go undetected. Although most are sporadic and non-recurrent, there is a subset comprising about 1% of all pregnancies which end with recurrent spontaneous abortion (RSA). This is defined as at least three consecutive miscarriages before 20 weeks of gestation (Matthiesen et al., 2012). RSA may have a number of causes (Harris, 2010; Beaman et al., 2012; Matthiesen et al., 2012), as molecular regulation of placentation is very complex, involving both promoting and inhibitory factors secreted by several cell types: decidual stromal cells, decidual macrophages, and decidual NK (dNK) cells (Knoefler and Pollheimer, 2012). Therefore, some of the cases may result from insufficient activity of dNK cells (Harris, 2010; Parham and Guethlein, 2010). NK cells constitute a large leukocyte population in the endometrium and they come in close contact with allogeneic extravillous trophoblast (EVT) cells in early pregnancy decidua, which is necessary for the placentation. EVT cells, in contrast to villous trophoblast cells, do express both maternal and paternal HLA-C molecules (Hiby et al., 2010). Moreover, HLA-C molecules on trophoblast cells form stable heterotrimeric heavy chain/β2-microglobulin/peptide complexes in contrast to decidual and other cells which express not only these heterotrimers, but also free HLA-C heavy chains (Apps et al., 2008). In addition, dNK cells are biased toward expression of HLA-C-binding KIRs (Male et al., 2011). Therefore, their polymorphic KIRs recognizing polymorphic HLA-C molecules inherited from the father by semiallogeneic fetus may play an important role in the outcome of pregnancy. Indeed, recent studies suggest that, in addition to their role in the innate immune response to infection and cancer, KIR-HLA (and particularly KIR-C1/C2) interactions control a proper formation of placenta (Chazara et al., 2011; Colucci et al., 2011; Parham et al., 2012b). Several investigators reported some associations of KIR genes with RSA.

First, Varla-Leftherioti et al. (2003) reported a comparison of 26 Greek couples with RSA and 26 fertile couples. They observed twice lower percentage of genotypes containing genes for all three HLA-C binding KIR2DL receptors in RSA couples as compared to control ones, and six times higher fraction of women not possessing KIR2DL genes present in their husbands (Varla-Leftherioti et al., 2003). These findings were confirmed on further 15 spontaneously aborting women compared with 15 women undergoing elective abortion from the Greek population; in addition, in 33.3% of spontaneously aborting women, fetal tissue did not possess a ligand for the inhibitory KIR(s) of the mother (Varla-Leftherioti et al., 2005). However, both these studies were performed on low numbers of patients and controls, and their results were not confirmed by the same authors on larger cohorts involving different ethnic groups (Varla-Leftherioti et al., 2007, 2010). Simultaneously, another group of investigators published a series of thorough studies on the English population, showing that: (a) KIR AA genotype frequency was significantly increased, and frequencies of B haplotype-associated KIR genes were decreased in 95 RSA cases compared to 269 controls (Hiby et al., 2008); (b) frequency of C2 group HLA-C alleles was significantly increased in male partners of RSA women, whereas these women exhibited an increased frequency of KIR AA genotype (which contains C2-specific KIR2DL1 gene; Hiby et al., 2008); and (c) KIR AA frequency was increased in affected mothers (i.e., combined mothers with preeclampsia, RSA, and restricted fetal growth) only when the fetus possessed more C2 genes than the mother, i.e., C2/C2 fetus in C1/C2 mother and C1/C2 fetus in C1/C1 mother (Hiby et al., 2010). This study showed also that the protective effect of haplotype B genes is located in telomeric part of the KIR region (TelB, containing KIR2DS1 gene), whereas no single gene from the haplotype A was found associated with RSA (Hiby et al., 2010). This latter result is not contradicting the association of AA genotype with RSA in England mentioned above, because all of A haplotype genes may appear also in some B haplotypes (Parham, 2005): both a centromeric (CenA) or telomeric (TelA) haplotype A segment may be linked to telomeric (TelB) or centromeric (CenB) segment from a B haplotype, respectively (Cooley et al., 2010; Parham and Guethlein, 2010; Pyo et al., 2010; Chazara et al., 2011), and only CenA/CenA-TelA/TelA genotypes were named “AA” in the past, all other ones being “BB” or “Bx.”

There were also reports on KIRs and HLA-C in RSA in other populations. Hong et al. (2008) described an association of KIR2DL2 (a B haplotype gene), but not any other KIR gene with RSA in Chinese (Hong et al., 2008). However, this study was made on extremely low number of patients (N = 16) and low number of controls (N = 41), and the result was not corrected for the number of comparisons. Indeed, another Chinese study on higher numbers of individuals (73 RSA couples and 68 control couples) did not confirm KIR2DL2 increase, but has rather shown an increase of activating KIR genes, 2DS1 and 2DS5 and association of RSA with higher numbers of activating KIRs (Wang et al., 2007). Similarly, in 68 Brazilian Caucasian RSA patients, genotypes with five or six activating KIR genes were significantly more frequent than in 68 controls (Vargas et al., 2009), although no single KIR gene reached significance in frequency distribution in this (Vargas et al., 2009) and other (Witt et al., 2004) study on Brazilian women. In northern India, two KIR A haplotype genes, 2DL1 and 2DS4, were found less frequently in 177 RSA patients than in 200 ethnically matched controls; a combination of KIR2DL1 in the mother with C2/C2 genotype in both parents was also less frequent in patients, whereas KIR2DL1 in the mother with C1/C1 genotype in both parents was more frequent in RSA couples than in controls. There were also some combinations of B haplotype-associated genes KIR2DS1 and KIR2DS2 with C1 and C2 genotypes which were differently distributed among RSA couples and controls (Faridi and Agrawal, 2011).

We typed 85 Polish Caucasian women with RSA and 117 healthy control women with at least two healthy born children for KIR genes and HLA-C C1 and C2 markers. We also tested their partners for HLA-C alleles and for C1 and C2. Similarly to some other investigators, we did not observe any differences in frequencies of individual KIR genes between RSA and control women (Nowak et al., 2011b). However, we found that genotypes with low activating to inhibitory KIR ratios were overrepresented in our RSA sample, whereas equilibrium between these two gene kinds seemed to favor a success of pregnancy (Nowak et al., 2009). Nevertheless, AA (most inhibitory) genotype was non-significantly less frequent in RSA than in control (Nowak et al., 2011b), and this result was confirmed by a significant decrease of this genotype in Turkish RSA patients (Ozturk et al., 2012). This result does not, again, seem to contradict the association of low activating to inhibitory KIR ratios with RSA mentioned above, because some inhibitory KIR genes (KIR2DL5A, KIR2DL5B) appear only in B haplotypes and therefore contribute to lower activating to inhibitory gene ratio, and some inhibitory KIR genes associated with A haplotype appear also in some B haplotypes, decreasing activating to inhibitory KIR ratio.

Furthermore, in our study women with AA KIR and C1C2 HLA-C genotype pregnant with C2C2 males were present in control but completely absent from the RSA group, whereas C1C1 and C2C2 AA women with C2C2 partners were absent from control but present in RSA (Nowak et al., 2011b). Our results are somewhat different from these of Hiby et al. (2010), where C1C2 AA women bearing C2C2 fetus were more frequent in affected pregnancies (RSA included) than in control, whereas we observed C1C2 AA women pregnant with C2C2 males only in control but not in RSA (Nowak et al., 2011b). Also, C1C1 AA women with C1C2 fetus were more frequent in affected group of Hiby et al. (2010), but C1C1 AA mothers with C1C2 father were more frequent in control than in RSA in our sample (Nowak et al., 2011b). These results can not be directly compared, however, as we had no possibility to HLA-C-type fetal tissue, particularly in our control, because elective termination of normal pregnancy is legally forbidden in Poland except for some criminal cases and endangered mother’s life. Therefore, in our case, we could predict fetal HLA-C genotype and its parental origin only for some couples (e.g., C1C1 mother and C2C2 father and vice versa).

In summary, results of studies published so far frequently bring conflicting results. The reasons for these discrepancies may be multiple. Some studied populations were genetically very distant, with different KIR and HLA-C genotype frequencies. This is exemplified by opposite results with KIR2DS1 association with RSA, negative in England (Hiby et al., 2008, 2010) but positive in China (Wang et al., 2007). In most studies the numbers of patients and controls were low, and extremely low in some reports, as shown in Table 3. Some associations detected in small population samples were not confirmed in larger cohorts. Also, criteria for inclusion of patients and controls were not the same, as we discussed elsewhere (Nowak et al., 2011b). Therefore, there seems to be a need for standardization of studies on genetics of RSA and other pregnancy disorders in different ethnic groups.

TABLE 3
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Table 3. KIR gene associations with recurrent spontaneous abortion.

An Intact KIR2DL4 Gene Does Not Seem Necessary for Female Fertility

KIR2DL4 differs from other KIR genes: (i) it has long cytoplasmic tail which, however, contains only one ITIM sequence; (ii) it has a positively charged arginine residue in the transmembrane region which gives it a possibility to make a complex with the FcεRIγ chain containing an ITAM sequence; (iii) it is not clonally distributed like other KIRs but expressed in all NK cells; (iv) on resting NK cells, it is expressed mostly not at the cell surface but in early endosomes where it can bind a soluble HLA-G molecule (its only known ligand), which is present (in physiological conditions) only on trophoblast cells invading decidua during early pregnancy; and it transmits an activating rather than inhibitory signal inducing cytokine secretion but not cytotoxicity (see a recent review by Rajagopalan and Long, 2012, and references therein).

KIR2DL4 is one of so called framework genes, present in all KIR haplotypes, similarly to KIR3DL2, KIR3DL3, and KIR3DP1 (Parham et al., 2012a). Therefore, interaction of KIR2DL4 expressed in dNK cells with HLA-G expressed by trophoblast was suspected to be very important for normal pregnancy (Carosella et al., 2001; Ober et al., 2003; Yan et al., 2007). However, healthy born individuals with defects of HLA-G gene were detected (Ober et al., 2003). Nevertheless, they were able to produce truncated form of HLA-G molecules which could substitute for the normal HLA-G (Hunt and Langat, 2009). Although KIR2DL4 gene was believed to be present in all people worldwide, several individuals lacking this gene were found in different populations in recent years. First one was an African immigrant from Bubi tribe (Bioko island, Equatorial Guinea), a woman who delivered five healthy children and experienced only one spontaneous abortion (Gomez-Lozano et al., 2003). Then, several single cases from Pakistan, Trinidad (also Pakistani by origin), South Turkey, and Solomon Islands were reported to the allele frequency database (Gonzalez-Galarza et al., 2011)3. We have also found, in the Polish population of 690 healthy individuals, one woman lacking KIR2DL4 gene (Nowak et al., 2011a). As her DNA was taken from paternity testing, she must have delivered at least one baby, and therefore was fertile. Interestingly, she had a KIR genotype identical to that of the Bubi woman mentioned above: 3DL3-2DS2-2DL2-2DL5B-(del)-2DS5-2DS1-3DL2. Unfortunately, her personal and family data must have remained anonymous, as required by the Bioethical Committee for samples from paternity testing, therefore neither studies on her family were possible nor data on her further reproductive success were available (Nowak et al., 2011a). However, her case, and particularly that of Bubi individual, indicate that the presence of KIR2DL4 gene is not absolutely necessary for successful human reproduction, similarly to the presence of intact HLA-G gene.

Neoplastic Diseases

Both NK cell cytotoxic activity (Herberman et al., 1975a,b; Kiessling et al., 1975a,b) and “missing-self” phenomenon (Ljunggren and Kärre, 1990) were discovered in experimental mouse models using tumor cells as targets for NK activity. Transformed neoplastic cells are believed to escape from elimination by cytotoxic T cells due to a reduction or loss of some or all HLA class I (HLA-I) molecules, which in turn exposes them to the attack from NK cells (Ljunggren and Kärre, 1990; Bubenik, 2004; Parham, 2005; Khakoo and Carrington, 2006; Purdy and Campbell, 2009). It has been shown that NK cells may lyze not only cells of established human tumor cell lines but also freshly isolated human tumor cells (Carlsten et al., 2009). Since KIR phenotype affects activity of NK cells (and subpopulations of T lymphocytes), one can expect that a prevalence of neoplasms may be influenced by it. Therefore, many investigators examined distribution of KIR genes and their ligands as well as their expression in several tumor systems, experimental and clinical (Parham, 2005; Khakoo and Carrington, 2006; van der Meer et al., 2008). We looked whether prevalence of non-small cell lung cancer (NSCLC) might be associated with genes for KIRs and their ligands in the Polish population.

Non-Small Cell Lung Cancer

Non-small cell lung cancer constitutes 85% of lung cancer cases which are a major cause of cancer mortality worldwide. It is a multifactorial disease with a strong environmental (mostly cigarette smoking) influence, but genetic factors also play a role4. In NSCLC, NK cells infiltrate rather peritumoral than tumor tissue, in contrast to T lymphocytes (Esendagli et al., 2008; Schneider et al., 2011), and these NK cells which do infiltrate the tumor are predominantly CD56bright, negative for NK cell receptors (including KIRs), and exhibit low cytotoxic activity ex vivo (Carrega et al., 2008; Esendagli et al., 2008). On the other hand, a tumor-specific cytotoxic T cell clone isolated from tumor infiltrating lymphocytes in an NSCLC patient expressed KIR3DL2 but not other KIRs, and KIR3DL2 had neither stimulating or inhibiting effect on its cytotoxic or interferon-gamma secreting activity (Dorothée et al., 2003). It was also shown that a majority of T cells infiltrating a tumor display T regulatory rather than effector cell phenotype (Esendagli et al., 2008; Schneider et al., 2011). Thus, cells infiltrating malignant areas in NSCLC seem to be poor in KIR expression and cytotoxic activity. Nevertheless, it is conceivable that cytotoxic effector cells, including NK, might eliminate or reduce numbers of potentially metastatic circulating cancer cells, as it has been described for uveal melanoma (Maat et al., 2009).

We typed 269 NSCLC patients for KIR and KIR ligand genes and compared the results with those of 690 unrelated healthy control individuals, all of them Polish Caucasians. No differences in the distribution of individual KIR genes or AA and Bx genotypes were observed (Wiśniewski et al., 2012). This finding confirms earlier report of Al Omar et al. (2010) in 186 NSCLC cases and 255 controls from England and Northern Ireland. However, we found less frequent prevalence of HLA-C C1/C2 genotype in patients than in controls, whereas both homozygotes were more frequent in patient group (Wiśniewski et al., 2012). This result was discordant with that of Al Omar et al. (2010), who did not observe any association of HLA-C C1 and C2 groups (encoding ligands for KIR2DL2/3 and KIR2DL1, respectively) with NSCLC, but found weak association of HLA-B Bw4Thr80 (coding for a ligand for KIR3DL1) which lost significance after correction. This was not, however, visible in our study (Wiśniewski et al., 2012). Interestingly, Al Omar et al. (2010) observed a protective effect of C1/C2 genotype on the prevalence of NSCLC, but only in the presence of KIR2DL3 gene, which we have not seen.

The reason for seemingly protective effect of C1/C2 genotype on NSCLC prevalence needs explanation. HLA-C molecules play two distinct roles in cellular immunity: first, they may present antigenic peptides to CD8+ T lymphocytes, although this their function seems less important than that of HLA-A and HLA-B; second, they protect normal cells of the body from the attack of NK cells equipped with HLA-C-binding inhibitory receptors such as KIR2DL1, KIR2DL2, and KIR2DL3. HLA-C molecules participate also in a process called “NK cell education”: these NK cells which possess inhibitory receptors binding self HLA class I molecules, including HLA-C, are “allowed” to mature, whereas NK cell clones devoid of such receptors remain immature and inactive (Björkström et al., 2010; Elliott and Yokoyama, 2011; Schönberg et al., 2011). Therefore, we can imagine that in NSCLC patients, individuals with C1/C2 genotype may have wider repertoire of antigenic peptides, including tumor antigens, presented to their HLA-C-restricted CD8+ cytotoxic T cells which can eradicate tumor cells. These individuals may also possess wider repertoire of HLA-C-educated NK cell clones which would eliminate these tumor cells which lost HLA-C expression. Transformed cells relatively frequently loose one HLA-C allele (Carretero et al., 2008; Mendez et al., 2009), including loss of heterozygosity in lung cancer (So et al., 2005). In C1/C1 and C2/C2 homozygotes, this does not change a sensitivity of cancer cells to NK-mediated lysis because they retain the same HLA-C allomorph encoded by the second chromosome and recognized by their mature NK cells. In this respect, C1/C2 individuals are in a privileged position, because even when a tumor cell retains one HLA-C allele, it is still vulnerable to lysis by these NK cells which express KIR recognizing a product of the second allele which had been lost (Maat et al., 2009).

Multivariate analysis revealed an effect of KIR and HLA-C genotype on the response of our patients to treatment (surgery and/or chemotherapy): KIR2DL2+, KIR2DS2+, C1/C1 individuals responded better to therapy and survived longer than patients with other genotypes (median survival time 23 months versus 10 months for patients with other genotypes; Wiśniewski et al., 2012).

Why the effect of KIR2DL2 and KIR2DS2 on treatment response and survival was seen only in the absence of C2 which is not their ligand (or a major ligand in the case of KIR2DL2, see Table 1)? Great majority (about 96%) of our patients (and controls as well) possessed KIR2DL1 gene whose product strongly interacts with C2+ HLA-C molecules (Parham, 2005; see Table 1). Therefore, in C2+ patients, NK cells expressing KIR2DL1 would be strongly inhibited and ineffective in C2+ tumor eradication. In individuals of KIR2DL2+, KIR2DS2+, C1/C1 genotype this interaction is not possible, therefore NK cells may be activated and kill tumor cells. KIR2DL2 interaction with C1 is much weaker than that of KIR2DL1 with C2 (Parham, 2005), so NK cell activation would not be so strongly inhibited. On the other hand, why C1/C1 genotype was not protective in the absence of KIR2DL2 and KIR2DS2 in our patients, is less clear. Perhaps activating KIR2DS2 receptor, whose ligand is not known (Table 1), is necessary for NK cell-mediated tumor cell lysis in this setting, but NK cells are not sufficiently inhibited by a weak KIR2DL2-C1 interaction. It is also possible that in some circumstances, e.g., when HLA-C C1 molecules are filled with a proper peptide, KIR2DS2 molecule may bind them strongly enough to activate the cell.

Our results suggest that NSCLC patients possessing KIR2DL2 and KIR2DS2 genes but not having C2 ligand for KIR2DL1 may respond better to treatment and survive longer than individuals bearing other genotypes. We also indicate that C1/C2 genotype may give some protection from the initiation of this tumor.

Viral Infections

Viruses infect cells and replicate inside them, forcing cell metabolism to produce abundant amounts of viral proteins. These are degraded to oligopeptides, bound by HLA class I molecules and presented to cytotoxic T cells (CD8+) like all other proteins produced within the cell (Neefjes et al., 2011). Therefore, many viruses evolved molecular mechanisms which interfere, in different ways, with cell surface expression of HLA class I molecules (Horst et al., 2011). This makes a virus-producing cell resistant to cytotoxic activity of T cells. On the other hand, the lack of one or all HLA class I molecules makes it susceptible to lysis by NK cells. This, however, depends on the repertoire of KIRs expressed on NK cell clones, which, in turn, depends on KIR genotype of the given individual (Parham, 2005; van Bergen and Koning, 2010). Associations of several types of viral infections and resulting human diseases with KIR genes have already been studied. Detailed review of the results of these studies would go beyond the acceptable volume of this article, therefore I will only mention here most important findings.

1. HIV-1 infection results in slower progression to AIDS in individuals possessing KIR3DS1 gene and HLA-Bw4 variant encoding isoleucine residue in position 80 (Martin et al., 2002a). This discovery stimulated multiple studies which are a topic of recent review (Koerner and Altfeld, 2012).

2. HIV-2 was much less extensively studied, because its prevalence is limited to West Africa, and its infection is more benign than that of HIV-1. No strong correlation with any KIR gene (including KIR3DS1) was observed, except for a trend for protective effect of KIR2DL2/KIR2DS2/C1 genotype (Yindom et al., 2010).

3. Both protective and detrimental effects of KIR2DL2 on human T-lymphotropic myelopathy/tropical spastic paraparesis in Japan, depending on HLA allele (Seich al Basatena et al., 2011).

4. Several KIR genes were found to be associated with H1N1 influenza 2009 pandemics (La et al., 2011; Aranda-Romo et al., 2012).

5. Mean number of activating KIRs per genotype was lowest in survivors of Ebola virus infection and highest in those with fatal outcome (Wauquier et al., 2010).

6. In human papillomavirus (HPV)-induced cervical intraepithelial neoplasia, protective effect of KIR3DL1 and KIR2DL1 in the presence of their ligands, and increased risk associated with KIR3DS1 was observed in Puerto Ricans and North Americans (Carrington et al., 2005), whereas only protection by KIR2DL5B was found in Swedish sample (Arnheim et al., 2005). In another HPV-induced disease, recurrent respiratory papillomatosis, KIR3DS1 together with KIR2DS1 appeared protective (Bonagura et al., 2010).

7. In HCMV infection of chronic hepatitis (Hepatitis B virus- or hepatitis C virus-induced) an expansion of NKG2C+ NK cells selectively expressing KIR2DL2 or KIR2DL3 was described (Beziat et al., 2012). In vasculitis complication of RA, CD4+CD28 T cells were observed only in patients infected with HCMV, suggesting a role for HCMV in boosting T cell autoreactivity (van Bergen and Koning, 2010).

8. Hepatitis B virus infection is common worldwide, particularly in China where it is a cause of the highest frequency of hepatocellular carcinoma (HCC) in the world (Zidan et al., 2012). A synergistic effect of a combined genotype C1C1+/Bw4-80I+/KIR2DS4fl+/KIR2DS4del+ on HCC risk was observed (Pan et al., 2011).

9. The role of KIR genes and molecules in HCV infection and HCV-induced HCC was so extensively studied that covering this topic would require a separate article. The protection from low-dose (injection or needle stick) but not from high-dose HCV infection was first described by Khakoo et al. (2004) in British Caucasoids and Afroamericans. The regulation of HCV infection by NK cells was briefly reviewed recently by Brenndörfer and Sällberg (2012).

General Remarks

The role of polymorphic NK cell receptors, KIRs, recognizing even more polymorphic HLA class I molecules, in human health and disease is gaining a constantly growing interest, and the number of publications is growing exponentially. This review could have touched only a fragment of this field.

Conflict of Interest Statement

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

Our work, mentioned here, was supported by the Ministry of Scientific Research and Information Technology grant 3 P05B 141 25, the Ministry of Science and Higher Education grants N402 078 31/2416, N401 077 31/1819, 2P05A 069 28, 2 PO5B 155 28, 2 P05B 048 27, N402 078 31/2416 and N N402 254936, the National Center of Science grant N402 685040, the Warsaw Medical University grant No. 1MB/W1/05, and the Ludwik Hirszfeld Institute of Immunology and Experimental Therapy grant No. 14 for years 2004–2012. I am indebted to all coauthors of my publications cited here for their contribution to them. I would express my special gratitude to Doctors Edyta Majorczyk, Izabela Nowak, and Andrzej Wiśniewski for critical reading of this manuscript. Generous agreement of all patients and control volunteers to donate blood and participate in these studies is gratefully acknowledged.

Footnotes

References

Al Omar, S., Middleton, D., Marshall, E., Porter, D., Xinarianos, G., Raji, O., et al. (2010). Associations between genes for killer immunoglobulin-like receptors and their ligands in patients with solid tumors. Hum. Immunol. 71, 976–981.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Albanesi, C., De Pità, O., and Girolomoni, G. (2007). Resident skin cells in psoriasis: a special look at the pathogenetic functions of keratinocytes. Clin. Dermatol. 25, 581–588.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Apps, R., Gardner, L., Hiby, S. E., Sharkey, A. M., and Moffett, A. (2008). Conformation of human leukocyte antigen-C molecules at the surface of human trophoblast cells. Immunology 124, 322–328.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Aranda-Romo, S., Garcia-Sepulveda, C. A., Comas-Garcia, A., Lovato-Salas, F., Salgado-Bustamante, M., Gómez-Gómez, A., et al. (2012). Killer-cell immunoglobulin-like receptors (KIR) in severe A (H1N1) 2009 influenza infection. Immunogenetics 64, 653–662.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Arnheim, L., Dillner, J., and Sanjeevi, C. B. (2005). A population-based cogort study of KIR genes and genotypes in relation to cervical intraepithelial neoplasia. Tissue Antigens 65, 252–259.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Beaman, K. D., Ntrivalas, E., Mallers, T. M., Jaiswal, M. K., Kwask-Kim, J., and Gilman-Sachs, A. (2012). Immune etiology of recurrent pregnancy loss and its diagnosis. Am. J. Reprod. Immunol. 67, 319–325.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Beziat, V., Dalgard, O., Asselah, T., Halfon, P., Bedossa, P., Boudifa, A., et al. (2012). CMV drives clonal expansion of NKG2C+ NK cells expressing self-specific KIRs in chronic hepatitis patients. Eur. J. Immunol. 42, 447–457.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Björkström, N. K., Riese, P., Heuts, F., Andersson, S., Fauriat, C., Ivarsson, M. A., et al. (2010). Expression patterns of NKG2A, KIR, and CD57 define a process of CD56dim NK-cell differentiation uncoupled from NK-cell education. Blood 116, 3853–3864.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Boguniewicz, M., and Leung, D. Y. M. (2011). Atopic dermatitis: a disease of altered skin barrier and immune dysregulation. Immunol. Rev. 242, 233–246.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bonagura, V. R., Du, Z., Ashouri, E., Luo, L., Hatam, L. J., DeVoti, J. A., et al. (2010). Activating killer cell immunoglobulin-like receptors 3DS1 and 2DS1 protect against developing the severe form of recurrent respiratory papillomatosis. Hum. Immunol. 71, 212–219.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bowes, J., and Barton, A. (2008). Recent advances in the genetics of RA susceptibility. Rheumatology 47, 399–402.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Boyton, R. J., and Altmann, D. M. (2007). Natural killer cells, killer immunoglobulin-like receptors and human leukocyte antigen class I in disease. Clin. Exp. Immunol. 149, 1–8.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Brenndörfer, E. D., and Sällberg, M. (2012). Hepatitis C virus-mediated modulation of cellular immunity. Arch. Immunol. Ther. Exp. (Warsz.) 60, 315–329.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bubenik, J. (2004). MHC class I down-regulation: tumor escape from immune surveillance? Int. J. Oncol. 25, 487–491.

Pubmed Abstract | Pubmed Full Text

Campbell, K. S., and Purdy, A. K. (2011). Structure/function of human killer cell immunoglobulin-like receptors: lessons from polymorphisms, evolution, crystal structures and mutations. Immunology 132, 315–325.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Carlsten, M., Malmberg, K.-J., and Ljunggren, H.-G. (2009). Natural killer cell-mediated lysis of freshly isolated human tumor cells. Int. J. Cancer 124, 757–762.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Carosella, E. D., Moreau, P., Aractingi, S., and Rouas-Freiss, N. (2001). HLA-G; a shield against inflammatory aggression. Trends Immunol. 22, 553–555.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Carrega, P., Morandi, B., Costa, R., Frumento, G., Forte, G., Altavilla, G., et al. (2008). Natural Killer cells infiltrating human non-small cell lung cancer are enriched in CD56 Bright CD16-cells and display an impaired capability to kill tumor cells. Cancer 112, 863–875.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Carretero, R., Romero, J. M., Ruiz-Cabello, F., Maleno, I., Rodriguez, F., Camacho, F. M., et al. (2008). Analysis of HLA class I expression in progressing and regressing metastatic melanoma lesions after immunotherapy. Immunogenetics 60, 439–447.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Carrington, M., Wang, S., Martin, M. P., Gao, X., Schiffman, M., Cheng, J., et al. (2005). Hierarchy of resistance to cervical neoplasia, mediated by combinations of killer immunoglobulin-like receptor and human leukocyte antigen loci. J. Exp. Med. 201, 1069–1075.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Chang, Y.-T., Chou, C.-T., Shiao, Y.-M., Lin, M.-W., Yu, C.-W., Chen, C.-C., et al. (2006). The killer cell immunoglobulin-like receptor genes do not confer susceptibility to psoriasis vulgaris independently in Chinese. J. Invest. Dermatol. 126, 2335–2338.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Chazara, O., Xiong, S., and Moffett, A. (2011). Maternal KIR and fetal HLA-C: a fine balance. J. Leukoc. Biol. 90, 703–716.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Choy, D. F., Hsu, D. K., Seshasayee, D., Fung, M. A., Modrusan, Z., Martin, F., et al. (2012). Comparative transcriptomic analyses of atopic dermatitis and psoriasis reveal shared neutrophilic inflammation. J. Allergy Clin. Immunol. 130, 1335–1343.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Colucci, F., Boulenouar, S., Kieckbusch, J., and Moffett, A. (2011). How does variability of immune system genes affect placentation? Placenta 32, 539–545.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Cooley, S., Weisdorf, D. J., Guethlein, L. A., Klein, J. P., Wang, T., Le, C. T., et al. (2010). Donor selection for natural killer cell receptor genes leads to superior survival after unrelated transplantation for acute myelogenous leukemia. Blood 116, 2411–2419.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Dalbeth, N., Gundle, R., Davies, R. J. O., Lee, Y. C. G., McMichael, A. J., and Callan, M. F. C. (2004). CD56bright NK cells are enriched at inflammatory sites and can engage with monocytes in a reciprocal program of activation. J. Immunol. 173, 6418–6426.

Pubmed Abstract | Pubmed Full Text

De Benedetto, A., Agnihothri, R., McGirt, L. Y., Bankova, L. G., and Beck, L. A. (2009). Atopic dermatitis: a disease caused by innate immune defects? J. Invest. Dermatol. 129, 14–30.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Dorothée, G., Echchakir, H., Le Maux Chansac, B., Vergnon, I., El Hage, F., Moretta, A., et al. (2003). Functional and molecular characterization of a KIR3DL2/p140 expressing tumor-specific T lymphocyte clone infiltrating a human lung carcinoma. Oncogene 22, 7192–7198.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Elliott, J. M., and Yokoyama, W. M. (2011). Unifying concepts of MHC-dependent natural killer cell education. Trends Immunol. 32, 364–372.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Esendagli, G., Bruderek, K., Goldmann, T., Busche, A., Branscheid, D., Vollmer, E., et al. (2008). Malignant and non-malignant lung tissue areas are differentially populated by natural killer cells and regulatory T cells in non-small cell lung cancer. Lung Cancer 59, 32–40.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Falgarone, G., Jaen, O., and Boissier, M. C. (2005). Role for innate immunity in rheumatoid arthritis. Joint Bone Spine 72, 17–25.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Faridi, R. M., and Agrawal, S. (2011). Killer immunoglobulin-like receptors (KIRs) and HLA-C allorecognition patterns implicative of dominant activation of natural killer cells contribute to recurrent miscarriages. Hum. Reprod. 26, 491–497.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Flores, A. C., Marcos, C. Y., Paladino, N., Arruvito, L., Williams, F., Middleton, D., et al. (2007). KIR receptors and HLA-C in the maintenance of pregnancy. Tissue Antigens 69(Suppl. 1), 112–113.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gilhar, A., Ullmann, Y., Kerner, H., Assy, B., Shalaginov, R., Serafimovich, S., et al. (2002). Psoriasis is mediated by a cutaneous defect triggered by activated immunocytes: induction of psoriasis by cells with natural killer receptors. J. Invest. Dermatol. 119, 384–391.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gomez-Lozano, N., de Pablo, R., Puente, S., and Vilches, C. (2003). Recognition of HLA-G by the NK cell receptor KIR2DL4 is not essential for human reproduction. Eur. J. Immunol. 33, 639–644.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Gonzalez-Galarza, F. F., Christmas, S., Middleton, D., and Jones, A. R. (2011). Allele frequency net: a database and online repository for immune gene frequencies in worldwide populations. Nucleic Acids Res. 39, D913–D919.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Graef, T., Moesta, A. K., Norman, P. J., Abi-Rached, L., Vago, L., Older-Aguilar, A. M., et al. (2009). KIR2DS4 is a product of gene conversion with KIR3DL2 that introduced specificity for HLA-A*11 while diminishing avidity for HLA-C. J. Exp. Med. 206, 2557–2572.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Guttman-Yasky, E., Nograles, K. E., and Krueger, J. G. (2011). Contrasting pathogenesis of atopic dermatitis and psoriasis – part II: immune cell subsets and therapeutic concepts. J. Allergy Clin. Immunol. 127, 1420–1432.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Harris, L. K. (2010). Review: trophoblast-vascular cell interactions in early pregnancy: how to remodel a vessel. Placenta 24, S93–S98.

CrossRef Full Text

Herberman, R. B., Nunn, M. E., Holden, H. T., and Lavrin, D. H. (1975a). Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic and allogeneic tumors. II. Characterization of effector cells. Int. J. Cancer 16, 230–239.

CrossRef Full Text

Herberman, R. B., Nunn, M. E., and Lavrin, D. H. (1975b). Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic and allogeneic tumors. I. Distribution of reactivity and specificity. Int. J. Cancer 16, 216–229.

CrossRef Full Text

Hiby, S. E., Apps, R., Sharkey, A. M., Farrell, L. E., Gardner, L., Mulder, A., et al. (2010). Maternal activating KIRs protect against human reproductive failure mediated by fetal HLA-C2. J. Clin. Invest. 120, 4102–4110.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hiby, S. E., Regan, L., Lo, W., Farrell, L., Carrington, M., and Moffett, A. (2008). Association of maternal killer-cell immunoglobulin-like receptors and parental HLA-C genotypes with recurrent miscarriage. Hum. Reprod. 23, 972–976.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Holm, S. J., Sakuraba, K., Mallbris, L., Wolk, K., Ståhle, M., and Sánchez, F. O. (2005). Distinct HLA-C/KIR genotype profile associates with guttate psoriasis. J. Invest. Dermatol. 125, 721–730.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hong, Y., Wang, X., Lu, P., Song, Y., and Lin, Q. (2008). Killer immunoglobulinlike receptor repertoire on uterine natural killer cell subsets in women with recurrent spontaneous abortions. Eur. J. Obstet. Gynecol. Reprod. Biol. 140, 218–223.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Horst, D., Verweij, M. C., Davison, A. J., Ressing, M. E., and Wiertz, E. J. (2011). Viral evasion of T cell immunity: ancient mechanisms offering new applications. Curr. Opin. Immunol. 23, 96–103.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hsu, K. C., Chida, S., Geraghty, D. E., and Dupont, B. (2002a). The killer cell immunoglobulin-like receptor (KIR) genomic region: gene order, haplotypes and allelic polymorphism. Immunol. Rev. 190, 40–52.

CrossRef Full Text

Hsu, K. C., Liu, X.-R., Selvakumar, A., Mickelson, E., O’Reilly, R. J., and Dupont, B. (2002b). Killer Ig-like receptor haplotype analysis by gene content. Evidence for genomic diversity with a minimum of six basic framework haplotypes, each with multiple subsets. J. Immunol. 169, 5123–5134.

Hunt, J. S., and Langat, D. L. (2009). HLA-G: a human pregnancy-related immunomodulator. Curr. Opin. Pharmacol. 9, 462–469.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Jacob, N., and Jacob, C. O. (2012). Genetics of rheumatoid arthritis: an impressionist perspective. Rheum. Dis. Clin. North Am. 38, 243–257.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Jobim, M., Jobim, L. F. J., Salim, P. H., Cestari, T. F., Toresan, R., Gil, B. C., et al. (2008). A study of the killer cell immunoglobulin-like receptor gene KIR2DS1 in a Caucasoid Brazilian population with psoriasis vulgaris. Tissue Antigens 72, 392–396.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kastelan, M., Prpic-Massari, L., and Brajac, I. (2009). Apoptosis in psoriasis. Acta Dermatovenerol. Croat. 17, 182–186.

Pubmed Abstract | Pubmed Full Text

Khakoo, S. I., and Carrington, M. (2006). KIR and disease: a model system or system of models? Immunol. Rev. 214, 186–201.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Khakoo, S., Thio, C. L., Martin, M. P., Brooks, C. R., Gao, X., Astemborski, J., et al. (2004). HLA and NK cell inhibitory receptor genes in resolving hepatitis C virus infection. Science 305, 872–874.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kiessling, R., Klein, E., and Wigzell, H. (1975a). “Natural” killer cells in the mouse. II. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Characteristics of the killer cell. Eur. J. Immunol. 5, 117–121.

CrossRef Full Text

Kiessling, R., Klein, E., and Wigzell, H. (1975b). “Natural” killer cells in the mouse. I. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Specificity and distribution according to genotype. Eur. J. Immunol. 5, 112–117.

CrossRef Full Text

Knoefler, M., and Pollheimer, J. (2012). IFPA award in placentology lecture: molecular regulation of human trophoblast invasion. Placenta 33, S55–S62.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Koerner, C., and Altfeld, M. (2012). Role of KIR3DS1 in human diseases. Front. Immunol. 3:326. doi:10.3389/fimmu.2012.00326

CrossRef Full Text

Kusnierczyk, P. (2006). “Sensing the self: structure, genetics, biological function and possible disease associations of KIR genes and molecules,” in Leading-Edge Immunology Research, ed. B. A. Veskler (New York: Nova Science Publishers, Inc.), 95–125.

La, D., Czarnecki, C., El-Gabalawy, H., Kumar, A., Meyers, A. F. A., Bastien, N., et al. (2011). Enrichment of variations in KIR3DL1/S1 and KIR2DL2/L3 among H1N1/09 ICU patients: an exploratory study. PLoS ONE 6:e29200. doi:10.1371/journal.pone.0029200

CrossRef Full Text

Lew, W., Bowcock, A. M., and Krueger, J. G. (2004). Psoriasis vulgaris: cutaneous lymphoid tissue supports T-cell activation and ‘Type 1’ inflammatory gene expression. Trends Immunol. 25, 295–305.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Liao, Y. H., Jee, S. H., Sheu, B. C., Huang, Y. L., Tseng, M. P., Hsu, S. M., et al. (2006). Increased expression of the natural killer cell inhibitory receptor CD94/NKG2A and CD158b on circulating and lesional T cells in patients with chronic plaque psoriasis. Br. J. Dermatol. 155, 318–324.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ljunggren, H.-G., and Kärre, K. (1990). In search of the ‘missing self’: MHC molecules and NK cell recognition. Immunol. Today 11, 237–244.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Luszczek, W., Kubicka, W., Cislo, M., Nockowski, P., Manczak, M., Woszczek, G., et al. (2002). Strong association of HLA-Cw6 allele with juvenile psoriasis in Polish patients. Immunol. Lett. 85, 59–64.

CrossRef Full Text

Luszczek, W., Manczak, M., Cislo, M., Nockowski, P., Wisniewski, A., Jasek, M., et al. (2004). Gene for the activating natural killer cell receptor, KIR2DS1, is associated with susceptibility to psoriasis vulgaris. Hum. Immunol. 65, 758–766.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Maat, W., van der Slik, A. R., Verhoeven, D. H. J., Alizadeh, B. Z., Ly, L. V., Verduijn, W., et al. (2009). Evidence for natural killer cell-mediated protection from metastasis formation in uveal melanoma patients. Invest. Ophthalmol. Vis. Sci. 50, 2888–2895.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Majorczyk, E., Pawlik, A., Luszczek, W., Nowak, I., Wisniewski, A., Jasek, M., et al. (2007). Associations of killer cell immunoglobulin-like receptor genes with complications of rheumatoid arthritis. Genes Immun. 8, 678–683.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Male, V., Sharkey, A., Masters, L., Kennedy, P. R., Farrell, L. E., and Moffett, A. (2011). The effect of pregnancy on the uterine NK cell KIR repertoire. Eur. J. Immunol. 41, 3017–3027.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Martin, M. P., Gao, X., Lee, J. H., Nelson, G. W., Detels, R., Goedert, J. J., et al. (2002a). Epistatic interaction between KIR3DS1 and HLA-B delays the progression to AIDS. Nat. Genet. 31, 429–434.

Martin, M., Nelson, G., Lee, J.-H., Pellett, F., Gao, X., Wade, J., et al. (2002b). Cutting edge: susceptibility to psoriatic arthritis: influence of activating killer Ig-like receptor genes in the absence of specific HLA-C alleles. J. Immunol. 169, 2818–2822.

Middleton, D., Meenagh, A., and Wright, G. D. (2007). No association in frequency of KIR receptors in patients with rheumatoid arthritis from Northern Ireland. Tissue Antigens 69, 577–582.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Matthiesen, L., Kalkunte, S., and Sharma, S. (2012). Multiple pregnancy failures: an immunological paradigm. Am. J. Reprod. Immunol. 67, 334–340.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Maxwell, L. D., Wallace, A., Middleton, D., and Curran, M. D. (2002). A common KIR2DS4 deletion variant in the human that predicts a soluble KIR molecule analogous to the KIR1D molecule observed in the rhesus monkey. Tissue Antigens 60, 254–258.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Maxwell, L. D., Williams, F., Gilmore, P., Meenagh, A., and Middleton, D. (2004). Investigation of killer cell immunoglobulin-like receptor gene diversity: II. KIR2DS4. Hum. Immunol. 65, 613–621.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

McErlean, C., Gonzalez, A. A., Cunningham, R., Meenagh, A., Shovlin, T., and Middleton, D. (2010). Differential RNA expression of KIR alleles. Immunogenetics 62, 431–440.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Mendez, R., Aptsiauri, N., Del Campo, A., Maleno, I., Cabrera, T., Ruiz-Cabello, F., et al. (2009). HLA and melanoma: multiple alterations in HLA class I and II expression in human melanoma cell lines from ESTDAB cell bank. Cancer Immunol. Immunother. 58, 1507–1515.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Neefjes, J., Jongsma, M. L., Paul, P., and Bakke, O. (2011). Towards a systems understanding of MHC class I and MHC class II antigen presentation. Nat. Rev. Immunol. 11, 823–836.

Pubmed Abstract | Pubmed Full Text

Nelson, G. W., Martin, M. P., Gladman, D., Wade, J., Trowsdale, J., and Carrington, M. (2004). Cutting edge: heterozygote advantage in autoimmune disease: hierarchy of protection/susceptibility conferred by HLA and killer Ig-like receptor combinations in psoriatic arthritis. J. Immunol. 173, 4273–4276.

Pubmed Abstract | Pubmed Full Text

Nomura, I., Gao, B., Boguniewicz, M., Darst, M. A., Travers, J. B., and Leung, D. Y. M. (2003). Distinct patterns of gene expression in the skin lesions of atopic dermatitis and psoriasis: a gene microarray analysis. J. Allergy Clin. Immunol. 112, 1195–1202.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Nowak, I., Majorczyk, E., Ploski, R., Senitzer, D., Sun, J. Y., and Kusnierczyk, P. (2011a). Lack of KIR2DL4 gene in a fertile Caucasian woman. Tissue Antigens 78, 115–119.

CrossRef Full Text

Nowak, I., Malinowski, A., Tchórzewski, H., Barcz, E., Wilczynski, J. R., Banasik, M., et al. (2011b). HLA-C C1C2 heterozygosity may protect women bearing the killer immunoglobulin-like receptor AA genotype from spontaneous abortion. J. Reprod. Immunol. 88, 32–37.

CrossRef Full Text

Nowak, I., Majorczyk, E., Wisniewski, A., Pawlik, A., Magott-Procelewska, M., Passowicz-Muszynska, E., et al. (2010). Does the KIR2DS5 gene protect from some human diseases? PLoS ONE 5:e12381. doi:10.1371/journal.pone.0012381

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Nowak, I., Malinowski, A., Tchórzewski, H., Barcz, E., Wilczynski, J. R., Grybos, M., et al. (2009). Frequencies of killer immunoglobulin-like receptor genotypes influence susceptibility to spontaneous abortion. J. Appl. Genet. 50, 391–398.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ober, C., Aldrich, C. L., Chervenova, I., Billstrand, C., Rahimov, F., Gray, H. L., et al. (2003). Variation in the HLA-G promoter region influences miscarriage rates. Am. J. Hum. Genet. 72, 1425–1435.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ozturk, O. G., Sahin, G., Ziyanoglu Karacor, E. D., and Kucukgoz, U. (2012). Evaluation of KIR genes in recurrent miscarriage. J. Assist. Reprod. Genet. 29, 933–938.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pan, N., Jiang, W., Sun, H., Miao, F., Qiu, J., Jin, H., et al. (2011). KIR and HLA loci are associated with hepatocellular carcinoma development in patients with hepatitis B virus infection: a case-control study. PLoS ONE 6:e25682. doi:10.1371/journal.pone.0025682

CrossRef Full Text

Parham, P. (2005). MHC class I molecules and KIRs in human history, health and survival. Nat. Rev. Immunol. 5, 201–214.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Parham, P., and Guethlein, L. A. (2010). Pregnancy immunogenetics: NK cell education in the womb? J. Clin. Invest. 120, 3801–3804.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Parham, P., Norman, P. J., Abi-Rached, L., and Guethlein, L. A. (2012a). Human-specific evolution of killer cell immunoglobulin-like receptor recognition of major histocompatibility complex class I molecules. Philos. Trans. R. Soc. Lond. B Biol. Sci. 367, 800–811.

CrossRef Full Text

Parham, P., Norman, P. J., Abi-Rached, L., Hilton, H. G., and Guethlein, L. A. (2012b). Review: immunogenetics of human placentation. Placenta 33, S71–S80.

CrossRef Full Text

Ploski, R., Luszczek, W., Kusnierczyk, P., Nockowski, P., Cislo, M., Krajewski, P., et al. (2006). A role for KIR gene variants other than KIR2DS1 in confering susceptibility to psoriasis. Hum. Immunol. 67, 521–526.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Purdy, A. K., and Campbell, K. S. (2009). Natural killer cells and cancer: regulation by the killer cell Ig-like receptors (KIR). Cancer Biol. Ther. 8, 13–22.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pyo, C.-W., Guethlein, L. A., Vu, Q., Wang, R., Abi-Rached, L., Norman, P. J., et al. (2010). Different patterns of evolution in the centromeric and telomeric regions of group A and group B haplotypes of the human killer cell Ig-like receptor locus. PLoS ONE 5:e15115. doi:10.1371/journal.pone.0015115

CrossRef Full Text

Rabin, R. L., and Levinson, A. I. (2008). The nexus between atopic disease and autoimmunity: a review of the epidemiological and mechanistic literature. Clin. Exp. Immunol. 153, 19–30.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Rajagopalan, S., and Long, E. O. (2012). KIR2DL4 (CD158d): an activation receptor for HLA-G. Front. Immun. 3:258. doi:10.3389/fimmu.2012.00258

CrossRef Full Text

Rebane, A., Zimmermann, M., Aab, A., Baurecht, H., Koreck, A., Karelson, M., et al. (2012). Mechanisms of IFN-γ-induced apoptosis of human skin keratinocytes in patients with atopic dermatitis. J. Allergy Clin. Immunol. 129, 1297–1306.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Schneider, T., Kimpfler, S., Warth, A., Schnabel, P. A., Dienemann, H., Schadendorf, D., et al. (2011). Foxp3+ regulatory T cells and natural killer cells distinctly infiltrate primary tumors and draining lymph nodes in pulmonary adenocarcinoma. J. Thorac. Oncol. 6, 432–438.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Schönberg, K., Sribar, M., Enczmann, J., Fischer, J. C., and Uhrberg, M. (2011). Analyses of HLA-C-specific KIR repertoires in donors with group A and B haplotypes suggest a ligand-instructed model of NK cell receptor acquisition. Blood 117, 98–107.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Seich al Basatena, N.-K., MacNamara, A., Vine, A. M., Thio, C. L., Astemborski, J., Usuku, K., et al. (2011). KIR2DL2 enhances protective and detrimental HLA class I-mediated immunity in chronic viral infection. PLoS Pathog. 7:e1002270. doi:10.1371/journal.ppat.1002270

CrossRef Full Text

Sivamani, R. K., Goodarzi, H., Shirakawa Garcia, M., Raychaudhuri, S. P., Wehrli, L. N., Ono, Y., et al. (2012). Biologic therapies in the treatment of psoriasis: a comprehensive evidence-based basic science and clinical review and a practical guide to tuberculosis monitoring. Clin. Rev. Allergy Immunol. doi:10.1007/s12016-012-8301-8307

CrossRef Full Text

So, T., Takenoyama, M., Mizukami, M., Ichiki, Y., Sugaya, M., Hanagiri, T., et al. (2005). Haplotype loss of HLA class I antigen as an escape mechanism from immune attack in lung cancer. Cancer Res. 65, 5945–5952.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Suzuki, Y., Hamamoto, Y., Ogasawara, Y., Ishikawa, K., Yoshikawa, Y., Sasazuki, T., et al. (2004). Genetic polymorphisms of killer cell immunoglobulin-like receptors are associated with susceptibility to psoriasis vulgaris. J. Invest. Dermatol. 122, 1133–1136.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Vales-Gomez, M., Reyburn, H. T., Erskine, R. A., and Strominger, J. (1998). Differential binding to HLA-C of p50-activating and p58-inhibitory natural killer cell receptors. Proc. Natl. Acad. Sci. U.S.A. 95, 14326–14331.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

van Bergen, J., and Koning, F. (2010). The tortoise and the hare: slowly evolving T-cell responses take hastily evolving KIR. Immunology 131, 301–309.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

van der Meer, A., Schaap, N. P. M., Schattenberg, A. V. M. B., van Cranenbroek, B., Tijssen, H. J., and Joosten, I. (2008). KIR2DS5 is associated with leukemia free survival after HLA identical stem cell transplantation in chronic myeloid leukemia patients. Mol. Immunol. 45, 3631–3638.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Vargas, R. G., Bompeixe, E. P., Pinhode Franca, P., Marques de Moraes, M., and da Graca Bicalho, M. (2009). Activating killer cell immunoglobulin-like receptor genes’ association with recurrent miscarriage. Am. J. Reprod. Immunol. 62, 34–43.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Varla-Leftherioti, M., Keramitsoglou, T., Spyropoulou-Vlachou, M., Papadimitropoulos, M., Kontopoulou-Antonopoulou, V., Tsekoura, C., et al. (2007). 14th International HLA and Immunogenetics Workshop: report from the reproductive immunology component. Tissue Antigens 69(Suppl. 1), 297–303.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Varla-Leftherioti, M., Keramitsoglu, T., Parapanissiou, E., Kurpisz, M., Kontopoulou-Antonopoulou, V., Tsekoura, C., et al. (2010). HLA-DQA1*0505 sharing and Killer immunoglobulin-like receptors in sub fertile couples: report of the 15th International Histocompatibility Workshop. Tissue Antigens 75, 668–672.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Varla-Leftherioti, M., Spyropoulou-Vlachou, M., Keramitsoglou, T., Papadimitropoulos, M., Tsekoura, C., Graphou, O., et al. (2005). Lack of the appropriate natural killer cell inhibitory receptors in women with spontaneous abortion. Hum. Immunol. 66, 65–71.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Varla-Leftherioti, M., Spyropoulou-Vlachou, M., Niokou, D., Keramitsoglou, T., Darlamitsou, A., Tsekoura, C., et al. (2003). Natural killer (NK) cell receptors’ repertoire in couples with recurrent spontaneous abortions. Am. J. Reprod. Immunol. 49, 183–191.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

von Bubnoff, D., Andrès, E., Hentges, F., Bieber, T., Michel, T., and Zimmer, J. (2010). Natural killer cells in atopic and autoimmune diseases of the skin. J. Allergy Clin. Immunol. 125, 60–68.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wang, S., Zhao, Y.-R., Jiao, Y.-L., Wang, L.-C., Li, J.-F., Cui, B., et al. (2007). Increased activating killer immunoglobulin-like receptor genes and decreased specific HLA-C alleles in couples with recurrent spontaneous abortion. Biochem. Biophys. Res. Commun. 360, 696–701.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wauquier, N., Padilla, C., Becquart, P., Leroy, E., and Wieillard, V. (2010). Association of KIR2DS1 and KIR2DS3 with fatal outcome in Ebola virus infection. Immunogenetics 62, 767–771.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Williams, F., Meenagh, A., Sleator, C., Cook, D., Fernandez-Vina, M., Bowcock, A. M., et al. (2005). Activating killer cell immunoglobulin-like receptor gene KIR2DS1 is associated with psoriatic arthritis. Hum. Immunol. 66, 836–841.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wiśniewski, A., Jankowska, R., Passowicz-Muszyńska, E., Wiśniewska, E., Majorczyk, E., Nowak, I., et al. (2012). KIR2DL2/S2 and HLA-C C1C1 genotype is associated with better response to treatment and prolonged survival of patients with non-small cel lung cancer in a Polish Caucasian population. Hum. Immunol. 73, 927–931.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Witt, C. S., Goodridge, J., Gerbase-Delima, M. G., Daher, S., and Christiansen, F. T. (2004). Maternal KIR repertoire is not associated with recurrent spontaneous abortion. Hum. Reprod. 19, 2653–2657.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Yan, W.-H., Lin, A., Chen, B.-G., Zhou, M.-Y., Dai, M.-Z., Chen, X.-J., et al. (2007). Possible roles of KIR2DL4 expression on uNK cells in human pregnancy. Am. J. Reprod. Immunol. 57, 233–242.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Yen, J. H., Moore, B. E., Nakajima, T., Scholl, D., Schaid, D. J., Weyand, C. M., et al. (2001). Major histocompatibility complex class I-recognizing receptors are disease risk genes in rheumatoid arthritis. J. Exp. Med. 193, 1159–1167.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Yindom, L.-M., Leligdowicz, A., Martin, M. P., Gao, X., Qi, Y., Zaman, S. M. A., et al. (2010). Influence of HLA class I and HLA-KIR compound genotypes on HIV-2 infection and markers of disease progression in a Manjako community in West Africa. J. Virol. 84, 8202–8208.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Zidan, A., Scheuerlein, H., Schuele, S., Settmacher, U., and Rauchfuss, F. (2012). Epidemiological pattern of hepatitis B and hepatitis C as etiological agents for hepatocellular carcinoma in Iran and worldwide. Hepat. Mon. 12, e6894.

Pubmed Abstract | Pubmed Full Text

Keywords: KIR genes, skin disease, rheumatoid arthritis, spontaneous abortion, cancer, viral diseases, viral infections

Citation: Kuśnierczyk P (2013) Killer cell immunoglobulin-like receptor gene associations with autoimmune and allergic diseases, recurrent spontaneous abortion, and neoplasms. Front. Immun. 4:8. doi: 10.3389/fimmu.2013.00008

Received: 28 September 2012; Accepted: 05 January 2013;
Published online: 29 January 2013.

Edited by:

Jeroen Van Bergen, Leiden University Medical Center, Netherlands

Reviewed by:

Stephan Gasser, National University of Singapore, Singapore
Jacques Zimmer, Centre de Recherche Public de la Santé, Luxembourg

Copyright: © 2013 Kuśnierczyk. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

*Correspondence: Piotr Kuśnierczyk, Laboratory of Immunogenetics and Tissue Immunology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, ul. Rudolfa Weigla 12, 53-114 Wrocław, Poland. e-mail: pkusnier@iitd.pan.wroc.pl

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