人类白细胞抗原
杂合子丢失
等位基因
杂合子优势
生物
遗传学
复合杂合度
免疫学
组织相容性
主要组织相容性复合体
HLA-B抗原
人类免疫缺陷病毒(HIV)
病毒学
基因
抗原
作者
Mary Carrington,George W. Nelson,Maureen P. Martin,Teri L. Kissner,David Vlahov,James J. Goedert,Richard A. Kaslow,Susan Buchbinder,Keith Hoots,Stephen J. O’Brien
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1999-03-12
卷期号:283 (5408): 1748-1752
被引量:1228
标识
DOI:10.1126/science.283.5408.1748
摘要
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 B*35 and Cw*04 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 B*35 and Cw*04 , or to both.
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