CD4-Like Immunological Function by CD4 − T Cells in Multiple Natural Hosts of Simian Immunodeficiency Virus

Author:

Vinton Carol1,Klatt Nichole R.1,Harris Levelle D.1,Briant Judith A.1,Sanders-Beer Brigitte E.2,Herbert Richard3,Woodward Ruth4,Silvestri Guido5,Pandrea Ivona6,Apetrei Cristian6,Hirsch Vanessa M.1,Brenchley Jason M.1

Affiliation:

1. Laboratory of Molecular Microbiology, NIAID, NIH, Bethesda, Maryland 20892

2. Bioqual, Rockville, Maryland 20850

3. Experimental Primate Virology Section, NIAID, NIH, Bethesda, Maryland 20892

4. NICHD, NIH, Bethesda, Maryland 20892

5. Division of Microbiology and Immunology, Emory University, Atlanta, Georgia 30322

6. Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania 15261

Abstract

ABSTRACT Many species of African nonhuman primates are natural hosts for individual strains of simian immunodeficiency virus (SIV). These infected animals do not, however, develop AIDS. Here we show that multiple species of African nonhuman primate species characteristically have low frequencies of CD4 + T cells and high frequencies of both T cells that express only the alpha-chain of CD8 and double-negative T cells. These subsets of T cells are capable of eliciting functions generally associated with CD4 + T cells, yet these cells lack surface expression of the CD4 protein and are, therefore, poor targets for SIV in vivo . These data demonstrate that coevolution with SIV has, in several cases, involved downregulation of receptors for the virus by otherwise-susceptible host target cells. Understanding the genetic factors that lead to downregulation of these receptors may lead to therapeutic interventions that mimic this modulation in progressive infections.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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