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

      Science (New York, N.Y.)
      Acquired Immunodeficiency Syndrome, genetics, immunology, Adult, Alleles, Antigen Presentation, Cohort Studies, Disease Progression, Ethnic Groups, Genes, MHC Class I, Genetic Predisposition to Disease, HIV Infections, HIV Long-Term Survivors, statistics & numerical data, HIV-1, HLA Antigens, HLA-B Antigens, HLA-C Antigens, Heterozygote, Homozygote, Humans, Killer Cells, Natural, Loss of Heterozygosity, Proportional Hazards Models, Risk

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          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 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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