Lewandowska Monika, Franciszkiewicz Katarzyna, Prokop Janusz, Ofori Harold, Jagodzinski Paweł P
Department of Biochemistry and Molecular Biology, University of Medical Sciences, Poznań, Poland.
J Hum Genet. 2002;47(11):585-9. doi: 10.1007/s100380200089.
Chemokine receptors (CCR2 and CXCR4) are used as coreceptors for entry of human immunodeficiency virus (HIV) into the target cells. Mutations in CCR2 (CCR2-64I) and stromal-derived factor SDF1 (SDF1-3'A), the primary ligand for CXCR4, exhibited a protective effect against the onset of acquired immune deficiency syndrome (AIDS). The frequency of the SDF1-3'A and CCR2-64I alleles were determined in blood donors from 16 provinces, covering the entire territory of Poland. Of 1063 individuals, 274 (25.8%) were carriers of the SDF1-3'A allele; 36 of them (3.4%) were homozygotes (SDF-3'A/A) while 238 (22.4%) were heterozygotes (SDF-3'G/A), resulting in a 14.6% frequency of the SDF1-3'A allele. Moreover, in the same group of individuals, 234 (22.0%) carried the CCR2-64I allele; 6 of them (0.6%) were homozygotes (CCR2-64I/I), and 228 (21.4%) were heterozygotes (CCR2-64V/I), resulting in an 11.3% frequency of the CCR2-64I allele. The highest frequencies of the SDF1-3'A allele were found in the northeastern provinces and in one of the western provinces of Poland. In contrast, allelic frequencies of CCR2-64I varied slightly among different provinces. The different pattern of prevalence of the SDF1-3'A and CCR2-64I alleles in Poland might suggest that the CCR2-64I allele was spread much earlier than the SDF1-3'A allele in the population of Poland.
趋化因子受体(CCR2和CXCR4)被用作人类免疫缺陷病毒(HIV)进入靶细胞的共受体。CCR2(CCR2 - 64I)和基质衍生因子SDF1(SDF1 - 3'A)(CXCR4的主要配体)中的突变对获得性免疫缺陷综合征(AIDS)的发病表现出保护作用。在覆盖波兰全境的16个省份的献血者中测定了SDF1 - 3'A和CCR2 - 64I等位基因的频率。在1063名个体中,274名(25.8%)是SDF1 - 3'A等位基因的携带者;其中36名(3.4%)是纯合子(SDF - 3'A/A),238名(22.4%)是杂合子(SDF - 3'G/A),导致SDF1 - 3'A等位基因频率为14.6%。此外,在同一组个体中,234名(22.0%)携带CCR2 - 64I等位基因;其中6名(0.6%)是纯合子(CCR2 - 64I/I),228名(21.4%)是杂合子(CCR2 - 64V/I),导致CCR2 - 64I等位基因频率为11.3%。SDF1 - 3'A等位基因的最高频率出现在波兰的东北部省份和西部的一个省份。相比之下,CCR2 - 64I的等位基因频率在不同省份之间略有差异。波兰SDF1 - 3'A和CCR2 - 64I等位基因的不同流行模式可能表明CCR2 - 64I等位基因在波兰人群中的传播比SDF1 - 3'A等位基因早得多。