Reappraisal of the Relationship between the HIV-1-Protective Single-Nucleotide Polymorphism 35 Kilobases Upstream of theHLA-CGene and Surface HLA-C Expression

Author:

Corrah Tumena W.1,Goonetilleke Nilu1,Kopycinski Jakub2,Deeks Steven G.3,Cohen Myron S.4,Borrow Persephone5,McMichael Andrew1,Brackenridge Simon1

Affiliation:

1. Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom

2. IAVI Human Immunology Laboratory, Imperial College London, London, United Kingdom

3. Department of Medicine, University of California San Francisco, San Francisco, California

4. Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina

5. Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom

Abstract

ABSTRACTPrevious studies have found an association between a single-nucleotide polymorphism 35 kb upstream of theHLA-Clocus (−35 SNP), HLA-C expression, and HIV-1 set point viral loads. We show that the difference in HLA-C expression across −35 SNP genotypes can be attributed primarily to the very low expression of a single allelic product, HLA-Cw7, which is a common HLA type. We suggest that association of the −35 SNP and HIV-1 load manifests as a result of linkage disequilibrium of this polymorphism with both favorable and unfavorable HLA-C and -B alleles.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference56 articles.

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