Major Histocompatibility Complex Genotype Is Associated with Disease Progression and Virus Load Levels in a Cohort of Human Immunodeficiency Virus Type 1–Infected Caucasians and African Americans
Author(s) -
Dean L. Mann,
Robin P. Garner,
Deborah E. Dayhoff,
Kai Cao,
Marcelo Fernández-Viña,
Charles E. Davis,
Naomi Aronson,
Nancy Ruíz,
Deborah L. Birx,
Nelson L. Michael
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/314519
Subject(s) - genotype , virology , cohort , virus , immunology , disease , major histocompatibility complex , human immunodeficiency virus (hiv) , biology , medicine , genetics , antigen , gene
To assess the influence of HLA on AIDS-free survival, human immunodeficiency virus load, and CD4 cell counts, 91 Caucasian and 48 African-American seroprevalent men were typed for HLA classes I and II and TAP alleles. HLA associations with these markers were assessed by assigning sum integer scores based on 7 class I allele-TAP variants (+1) and 13 class I-class II-TAP combinations (-1) with different AIDS-free survival times found in a prior study. Subjects in both racial groups and combined with positive sum scores were less likely to have CD4 cell decline (P=.0004), to have increased virus burden (P=.014), and to develop AIDS (P=.034) in the follow-up period than were Caucasians and African Americans with scores of 0 or -1. These results confirm the reported associations of specific major histocompatibility complex genes with AIDS-free survival time in Caucasians and specifically extend them to African Americans and to two established markers of disease progression.
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