The −1030/−862-linked TNF promoter single-nucleotide polymorphisms are associated with the inability to control HIV-1 viremia

Immunogenetics - Tập 55 - Trang 497-501 - 2003
Julio C. Delgado1,2, Jessica Y. Leung1, Andres Baena1, Olga P. Clavijo1, Eric Vittinghoff3, Susan Buchbinder3,4, Steven Wolinsky5, Marilynn Addo6, Bruce D. Walker6, Edmond J. Yunis7, Anne E. Goldfeld1,8
1Center for Blood Research, Boston, USA
2Department of Pathology, Brigham and Women’s Hospital, Boston, USA
3Department of Epidemiology and Statistics, University of California, San Francisco, USA
4San Francisco Department of Public Health, San Francisco, USA
5Department of Medicine, Northwestern University Medical School, Chicago, USA
6Partners AIDS Research Center, Massachusetts General Hospital, Boston, USA
7Division of Immunology and AIDS, Dana-Farber Cancer Institute, Boston, USA
8Department of Medicine, Brigham and Women’s Hospital, Boston, USA

Tóm tắt

Control of HIV-1 viremia and progression to AIDS has been associated with specific HLA genes. The tumor necrosis factor (TNF) and the non-classical major histocompatibility (MHC) class I chain-related A (MICA) genes are located in the genomic segment between the HLA class I and II genes and variants of both genes have been identified. We thus analyzed TNF promoter and MICA variants in a well-characterized group of HIV-1 infected individuals with different abilities to control HIV-1 viremia. In our cohort, the −1030/−862-linked TNF promoter single-nucleotide polymorphisms (SNPs), but not MICA variants, are significantly associated with lack of control of HIV-1 viremia (P=0.03). This association is independent of those HLA-B35 alleles associated with HIV-1 disease progression with which the −862 TNF SNP has previously been independently associated. Thus, non-randomly associated genes near the TNF locus are likely involved in control of HIV-1 viremia.

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