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人类白细胞抗原与人类免疫缺陷病毒1型:杂合子优势及B*35-Cw*04劣势

HLA and HIV-1: heterozygote advantage and B*35-Cw*04 disadvantage.

作者信息

Carrington M, Nelson G W, Martin M P, Kissner T, Vlahov D, Goedert J J, Kaslow R, Buchbinder S, Hoots K, O'Brien S J

机构信息

Intramural Research Support Program, Science Applications International Corporation Frederick, National Cancer Institute (NCI), Frederick, MD 21702-1201, USA.

出版信息

Science. 1999 Mar 12;283(5408):1748-52. doi: 10.1126/science.283.5408.1748.

Abstract

A selective advantage against infectious disease associated with increased heterozygosity at the human major histocompatibility complex [human leukocyte antigen (HLA) class I and class II] is believed to play a major role in maintaining the extraordinary allelic diversity of these genes. Maximum HLA heterozygosity of class I loci (A, B, and C) delayed acquired immunodeficiency syndrome (AIDS) onset among patients infected with human immunodeficiency virus-type 1 (HIV-1), whereas individuals who were homozygous for one or more loci progressed rapidly to AIDS and death. The HLA class I alleles B35 and Cw04 were consistently associated with rapid development of AIDS-defining conditions in Caucasians. The extended survival of 28 to 40 percent of HIV-1-infected Caucasian patients who avoided AIDS for ten or more years can be attributed to their being fully heterozygous at HLA class I loci, to their lacking the AIDS-associated alleles B35 and Cw04, or to both.

摘要

人类主要组织相容性复合体(人类白细胞抗原I类和II类)杂合性增加与抵抗传染病的选择优势,被认为在维持这些基因异常的等位基因多样性方面发挥着重要作用。I类基因座(A、B和C)的最大HLA杂合性延缓了感染1型人类免疫缺陷病毒(HIV-1)患者后天免疫缺陷综合征(AIDS)的发病,而一个或多个基因座纯合的个体则迅速发展为AIDS并死亡。HLA I类等位基因B35和Cw04始终与白种人AIDS确诊疾病的快速发展相关。28%至40%的HIV-1感染白种人患者避免AIDS达十年或更长时间,其延长的生存期可归因于他们在HLA I类基因座完全杂合、缺乏与AIDS相关的等位基因B35和Cw04,或两者皆有。

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