期刊文献+

辅助受体CCR5、CCR2及细胞趋化因子SDF1基因多态性与HIV-1异性传播的关系 被引量:2

Impact of the polymorphisms of CCR5,CCR2 and SDF1 on HIV-1 heterosexual transmission
原文传递
导出
摘要 目的 进一步阐述CCR5、CCR2和SDF1基因多态性与HIV 1异性传播的关系。方法 通过PCR RFLP技术分析CCR5、CCR2和SDF1基因的多态性 ,继而分析基因多态性与HIV 1异性传播的关系。结果 在收集到的 70对异性配对病例中 ,未能在汉族人群发现CCR5基因缺失突变 ,维吾尔族人CCR5Δ32基因频率为 6 .5 % (6 92 ) ,未发现纯合突变。有暴露史而未感染HIV 1者CCR2 6 4I基因频率明显高于受暴露后感染病毒者 ,说明CCR2 6 4I对异性传播可能具有一定保护作用。对SDF1基因的多态性研究发现 ,将病毒传播给配偶的指标病例 (先感染HIV 1一方 )SDF1 3′A的基因频率高于未发生传播者 (较接近于统计学检验水准 ) ,SDF1 3′A似乎是危险因素。结论 CCR5Δ32对汉族人群的HIV 1异性传播无明显意义 ,CCR2 6 4I对HIV 1异性传播可能具有一定的保护作用 ,而SDF1 3′A则有可能是危险因素 ,但有必要扩大样本量对后二者作进一步的深入研究。 Objective To investigate the impact of the polymorphisms of CCR5, CCR2 and SDF1 on HIV-1 heterosexual transmission. Methods The polymorphisms of CCR5, CCR2 and SDF1 were displayed by PCR/RFLP and carefully assessed as influential factors on HIV-1 heterosexual transmission. Results The deletion of CCR5 in the coding region (CCR5Δ32) wasn′t found in Han Chinese in this cohort, but the frequency of CCR5Δ32 was 6.5%(6/92) in Uygur people (no allele of CCR5Δ32/Δ32). The data didn′t sound the role of CCR5Δ32 in HIV-1 heterosexual transmission in China. On the other hand, a higher frequency of CCR2-64I allele was observed in HIV-1 uninfected partners who were heterosexually exposed to HIV-1 positive index partners than those infected with HIV-1 ( P =0.164). However, a higher frequency of SDF1-3′A allele was found in HIV-1 positive index individuals with HIV-1 positive partners than those with negative partners ( P =0.163). Conclusion Heterozygous allele of CCR5 (CCR5 +/Δ32) is not substantially supposed to influence HIV-1 heterosexual transmission in China. CCR2-64I may play a role in protecting from HIV-1 heterosexual transmission, but SDF1-3′A seems to be a risk factor.
出处 《中华微生物学和免疫学杂志》 CAS CSCD 北大核心 2003年第10期773-777,共5页 Chinese Journal of Microbiology and Immunology
关键词 辅助受体 CCR5 CCR2 细胞趋化因子 SDFl 基因多态性 HIV-1 异性传播 艾滋病 HIV-1 Co-receptor Polymorphism Heterosexual transmission
  • 相关文献

同被引文献30

  • 1邓小玲 ,洪坤学 ,陈健平 ,阮玉华 ,许铭炎 ,秦光明 ,李克 ,邢辉 ,邵一鸣 .四川彝族人群HIV-1辅助受体CCR5△32和CCR2-64I基因多态性分析[J].中华流行病学杂志,2004,25(12):1050-1053. 被引量:15
  • 2Michael NL, Louie LG, Rohrbaugh AL, et al. The role of CCR5 and CCR2 polymorphisms in HIV-1 transmission and disease progression[J]. Nat Med, 1997, 3(10): 1160-2.
  • 3Dean M, Carrington M, Winkler C, et al. Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Hemophilia Growth and Development Study, Multicenter AIDS Cohort Study, Multicenter Hemophilia Cohort Study, San Francisco City Cohort, ALIVE Study [J]. Science, 1996, 273(5283): 1856-62.
  • 4Hoffman TL, MacGregor RR, Burger H, et al. CCR5 genotypes in sexually active couples discordant for human immunodeficiency virus type 1 infection status[J]. J Infect Dis, 1997, 176(4): 1093-6.
  • 5Sullivan AD, Wigginton J, Kirschner D. The coreceptor mutation CCR5Delta32 influences the dynamics of HIV epidemics and is selected for by HIV[J]. Proc Natl Acad Sci U S A, 2001, 98(18): 10214-9.
  • 6冯铁建,陈琳,王福生,等.艾滋病病人及其密切接触者HIV-1抗性基因多态性及其病程发展间关系分析[c].第一届中国艾滋病性病防治大会论文集.2001.
  • 7Wang FS, Hong WG, Cao YZ, et al. Population survey of CCR5 A 32, CCR5 m303, CCR2b 64I, and SDF13'A allele frequencies in indigenous Chinese healthy individuals, and in HIV-1-infected and HIV-1-uninfected individuals in HIV-1 risk groups [J]. J Acquir Immune Defic Syndr, 2003, 32(2): 124-30.
  • 8Wang YY, Wang XH, Peng J, et al. SDF1-3'A gene mutation is correlated with increased susceptibility to HIV type 1 infection by sexual transmission in Han Chinese [J]. AIDS Res Hum Retroviruses, 2008, 24(11): 1341-5.
  • 9Xu LD, Qiao YD, Zhang XL, et al. CCR2-64I allele is associated with the progression of AIDS in a Han Chinese population[J]. Mol Biol Rep, 2010, 37(1): 311-6.
  • 10Tan XH, Zhang JY, Di CH, et al. Distribution of CCR5-A 32, CCR5m303A, CCR2-64I and SDF1-3'A in HIV-linfected and uninfected high-risk Uighurs in Xinjiang, China [J]. Infection, Genetics and Evolution, 2010, 10(2): 268-72.

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部