Bharti Deepak, Kumar Ashish, Mahla Ranjeet Singh, Kumar Sushil, Ingle Harshad, Yadav Tushar, Mishra Anamika, Raut Ashwin Ashok, Kumar Himanshu
Laboratory of Immunology, Department of Biological Sciences, Indian Institute of Science Education and Research (IISER), Indore-Bypass Road, Bhauri, Bhopal, 460066 India.
Chemical Engineering Department, Sardar Vallabhbhai National Institute of Technology, Surat, 395007 India.
Springerplus. 2015 Aug 25;4:451. doi: 10.1186/s40064-015-1238-6. eCollection 2015.
Human immunodeficiency virus-1 (HIV-1) which causes acquired immune deficiency syndrome (AIDS), by infecting CD4(+) immune cells and hence weakening the host defense mechanism till death, is one of the major factor responsible for human demises worldwide. Both innate (monocytes and macrophages) and adaptive (T cells) immune cells expresses chemokines receptors (2 and 5) and stromal cell derived factor-1 (SDF-1) which play crucial role in HIV-1 virus entry and progression. Allele variants of genes CCR5 (CCR5-Δ32), CCR2 (CCR2-64I) and SDF1 (SDFA-3'A; the ligand of CXCR4) are known to slow down the HIV-1 progression in infected individual. In the present study, the frequency of CCR5-Δ32, CCR2-64I and SDF1-3'A alleles in primitive tribe (Baiga) and a non-primitive tribe (Gond) of central India were investigated. A total 200 seronegative samples for HIV from healthy individuals of tribes were analyzed and observed allele frequencies of CCR5-Δ32, CCR2-64I and SDF1-3'A were (0, 0.035, 0.080) and (0, 0.110, 0.100) in Baiga and Gond respectively. Minor allele frequency of these alleles of Gond and Baiga tribes were compared with different populations of the world for relative hazard (RH), which indicate the risk of progression after infection of HIV1. The RH values were calculated based on genotypic frequency, showed the high RH value (RH1-AIDS1993-0.98, RH2-AIDS1987-0.98 and death/RH3-0.97) in Baiga tribe, indicates the low level of resistance against HIV-1 progression after infection.
导致获得性免疫缺陷综合征(艾滋病)的人类免疫缺陷病毒1型(HIV-1),通过感染CD4(+)免疫细胞,从而削弱宿主防御机制直至死亡,是全球人类死亡的主要因素之一。先天免疫细胞(单核细胞和巨噬细胞)和适应性免疫细胞(T细胞)均表达趋化因子受体(2型和5型)以及基质细胞衍生因子-1(SDF-1),它们在HIV-1病毒进入和病程发展中发挥关键作用。已知基因CCR5(CCR5-Δ32)、CCR2(CCR2-64I)和SDF1(SDFA-3'A;CXCR4的配体)的等位基因变体可减缓HIV-1在受感染个体中的病程发展。在本研究中,调查了印度中部原始部落(拜加人)和非原始部落(贡德人)中CCR5-Δ32、CCR2-64I和SDF1-3'A等位基因的频率。对来自部落健康个体的总共200份HIV血清阴性样本进行了分析,结果显示,拜加人和贡德人中CCR5-Δ32、CCR2-64I和SDF1-3'A的观察等位基因频率分别为(0,0.035,0.080)和(0,0.110,0.100)。将贡德部落和拜加部落这些等位基因的次要等位基因频率与世界不同人群进行比较,以确定相对风险(RH),这表明感染HIV1后疾病进展的风险。基于基因型频率计算得出的RH值显示,拜加部落的RH值较高(RH1-AIDS1993-0.98,RH2-AIDS1987-0.98和死亡/RH3-0.97),表明其感染HIV-1后疾病进展的抵抗水平较低。