Mutuiri Shem P M, Kutima Helen L, Mwapagha Lamech M, Munyao James K, Nyamache Anthony Kebira, Wanjiru Irene, Khamadi Samoel A
Institute of Tropical Medicine and Infectious Diseases, Jomo Kenyatta University of Agriculture and Technology, Juja, Kenya.
Institute of Biotechnology, Jomo Kenyatta University of Agriculture and Technology, Juja, Kenya.
Dis Markers. 2016;2016:4703854. doi: 10.1155/2016/4703854. Epub 2016 Oct 16.
Previous studies have reported that two single nucleotide polymorphisms (SNPs) in the RANTES gene promoter region, -403G/A and -28C/G, are associated with a slower rate of decline in CD4+ T cell count. In addition, as a ligand of the major HIV coreceptor CCR5, it is known to block HIV-CCR5 interactions in the course of the HIV infection cycle. This study was carried out with the aim of determining the occurrence of single nucleotide polymorphisms (SNPs) -403G > A and -28C > G in the promoter region of RANTES, in a subset of the Kenyan population. Genomic DNA was extracted from peripheral blood monocular cells and used to amplify the RANTES gene region. Restriction fragment length polymorphism was used to determine the genotypes of the RANTES gene. Out of 100 HIV infected individuals, 19% had G1 genotypes (403G/G, 28C/G), 30% (403A/A, 28C/C), and 50% (403G/A, 28C/C), while in healthy blood donors 13% had G4 (403G/A, 28C/C) genotypes, 22% (403A/A, 28C/C), and 54% (403G/A, 28C/C). HIV negative blood donors (54%) had higher risk of alteration to risk of HIV transmission compared to those who were HIV infected (50%). However, the risk to transmission and distribution differences was not significant ( = 0.092). The study showed that RANTES polymorphisms -403 and -28 alleles do exist in the Kenyan population.
先前的研究报告称,RANTES基因启动子区域的两个单核苷酸多态性(SNP),即-403G/A和-28C/G,与CD4+T细胞计数下降速度较慢有关。此外,作为主要HIV共受体CCR5的配体,已知其在HIV感染周期过程中可阻断HIV与CCR5的相互作用。本研究旨在确定肯尼亚部分人群RANTES启动子区域单核苷酸多态性(SNP)-403G>A和-28C>G的发生情况。从外周血单核细胞中提取基因组DNA,并用于扩增RANTES基因区域。采用限制性片段长度多态性来确定RANTES基因的基因型。在100名HIV感染者中,19%具有G1基因型(403G/G,28C/G),30%(403A/A,28C/C),50%(403G/A,28C/C);而在健康献血者中,13%具有G4(403G/A,28C/C)基因型,22%(403A/A,28C/C),54%(403G/A,28C/C)。HIV阴性献血者(54%)相比HIV感染者(50%)有更高的改变为HIV传播风险的可能性。然而,传播风险和分布差异不显著(P=0.092)。该研究表明,RANTES基因多态性-403和-28等位基因在肯尼亚人群中确实存在。