Department of Immunology, School of Biological Sciences, Madurai Kamaraj University, Madurai.
Immunogenetics and Transplantation Laboratory, Department of Surgery, University of California, San Francisco, California, USA.
AIDS. 2018 Nov 28;32(18):2679-2688. doi: 10.1097/QAD.0000000000002028.
To investigate the role of genotypic and phenotypic characteristics of killer cell immunoglobulin-like receptors (KIRs) and their human leukocyte antigen (HLA) class-1 ligands in HIV-1 disease progression.
This is a nested case-control study including 347 HIV seropositive (HIV-1+) individuals from South India constituting 45 long-term nonprogressors (LTNPs) and 302 disease progressors. KIR genotyping was performed by multiplex sequence-specific primer-directed PCR (SSP-PCR). Phenotypic expressions of KIR3DL1/S1 was studied using multiparametric flow cytometry assay. HLA-Bw4 and Bw6 epitopes were determined by ARMS-PCR. HLA-Bw4I80, HLA-Bw4T80, HLA-C1, HLA-C2, and HLA-Aw4 were genotyped using SSP-PCR. Serum levels of IFN-γ was quantified using ELISA method.
Overall, 37 different KIR genotypes were observed and the distribution of genotypes with AB-AB (OR = 2.2, P = 0.033) constellations showed significant increase among LTNPs. The frequencies of 3DL1-2DL3-2DL5 (OR = 2.2, Pc = 0.031), 3DL1-Bw4/Aw4 (OR = 2.49, Pc = 0.019), homozygous Bw4 (OR = 2.422, Pc = 0.011) were observed higher in LTNPs and 2DS1-2DS2-2DS3 (OR = 0.475, Pc = 0.03), homozygous Bw6 (OR = 0.413, Pc = 0.011) were higher in the disease progressors. Flow cytometry assay showed the increased expression and maintenance of 3DL1/S1+NK cells in LTNPs (P = 0.0001). Further the expansion of 3DS1+NK cells was higher than 3DL1+NK cells in the heterozygous 3DL1/S1 LTNPs (P = 0.001).
The inhibitory receptor 3DL1 with Bw4 and its A-haplotype defining KIR genes (2DL3/L5) confers protection against HIV-1 disease progression. An increased expression and maintenance of 3DL1/S1+ natural killer cells may contribute to the efficient activation of the natural killer cells and subsequent long-term nonprogression (LTNPn) to the disease.
研究杀伤细胞免疫球蛋白样受体(KIR)的基因型和表型特征及其与人类白细胞抗原(HLA)I 类配体在 HIV-1 疾病进展中的作用。
这是一项嵌套病例对照研究,包括来自印度南部的 347 名 HIV 血清阳性(HIV-1+)个体,其中包括 45 名长期非进展者(LTNP)和 302 名疾病进展者。通过多重序列特异性引物导向 PCR(SSP-PCR)进行 KIR 基因分型。使用多参数流式细胞术测定 KIR3DL1/S1 的表型表达。通过 ARMS-PCR 确定 HLA-Bw4 和 Bw6 表位。使用 SSP-PCR 对 HLA-Bw4I80、HLA-Bw4T80、HLA-C1、HLA-C2 和 HLA-Aw4 进行基因分型。使用 ELISA 法定量血清 IFN-γ 水平。
总体上观察到 37 种不同的 KIR 基因型,AB-AB(OR=2.2,P=0.033)组合的基因型分布在 LTNPs 中显著增加。3DL1-2DL3-2DL5(OR=2.2,Pc=0.031)、3DL1-Bw4/Aw4(OR=2.49,Pc=0.019)、纯合 Bw4(OR=2.422,Pc=0.011)的频率在 LTNPs 中更高,2DS1-2DS2-2DS3(OR=0.475,Pc=0.03)、纯合 Bw6(OR=0.413,Pc=0.011)的频率在疾病进展者中更高。流式细胞术检测显示,LTNPs 中 3DL1/S1+NK 细胞的表达和维持增加(P=0.0001)。进一步的是,杂合 3DL1/S1 LTNPs 中 3DS1+NK 细胞的扩增高于 3DL1+NK 细胞(P=0.001)。
具有 Bw4 的抑制性受体 3DL1 及其 A 单倍型定义的 KIR 基因(2DL3/L5)可防止 HIV-1 疾病进展。3DL1/S1+自然杀伤细胞的表达和维持增加可能有助于自然杀伤细胞的有效激活,并随后导致长期非进展(LTNPn)至疾病。