Paucity of CD4+CCR5+ T cells is a typical feature of natural SIV hosts

Author:

Pandrea Ivona1,Apetrei Cristian1,Gordon Shari23,Barbercheck Joseph1,Dufour Jason1,Bohm Rudolf1,Sumpter Beth3,Roques Pierre4,Marx Preston A.1,Hirsch Vanessa M.5,Kaur Amitinder6,Lackner Andrew A.1,Veazey Ronald S.1,Silvestri Guido23

Affiliation:

1. Tulane National Primate Research Center, Covington, LA;

2. Department of Pathology, University of Pennsylvania, Philadelphia, PA;

3. Yerkes National Primate Research Center, Atlanta, GA;

4. Centre International de Recherches Medicales, Franceville, Gabon;

5. Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD;

6. New England Primate Research Center, Southborough, MA

Abstract

AbstractIn contrast to lentiviral infections of humans and macaques, simian immunodeficiency virus (SIV) infection of natural hosts is nonpathogenic despite high levels of viral replication. However, the mechanisms underlying this absence of disease are unknown. Here we report that natural hosts for SIV infection express remarkably low levels of CCR5 on CD4+ T cells isolated from blood, lymph nodes, and mucosal tissues. Given that this immunologic feature is found in 5 different species of natural SIV hosts (sooty mangabeys, African green monkeys, mandrills, sun-tailed monkeys, and chimpanzees) but is absent in 5 nonnatural/recent hosts (humans, rhesus, pigtail, cynomolgus macaques, and baboons), it may represent a key feature of the coevolution between the virus and its natural hosts that led to a nonpathogenic infection. Beneficial effects of low CCR5 expression on CD4+ T cells may include the reduction of target cells for viral replication and a decreased homing of activated CD4+ T cells to inflamed tissue.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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