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Blood, 1 February 2007, Vol. 109, No. 3, pp. 1069-1076.
Prepublished online as a Blood First Edition Paper on September 26, 2006; DOI 10.1182/blood-2006-05-024364.


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Submitted May 18, 2006
Accepted September 14, 2006

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

Ivona Pandrea*, Cristian Apetrei, Shari N Gordon, Joseph Barbercheck, Jason Dufour, Rudolf Bohm, Beth S Sumpter, Pierre Roques, Preston A Marx, Vanessa M Hirsch, Amitinder Kaur, Andrew A Lackner, Ronad S Veazey, and Guido Silvestri

Tulane National Primate Research Center, Covington, LA
Yerkes National Primate Research Center, Atlanta, GA,
Centre International de Recherches Medicales, Franceville, Gabon
Laboratory of Molecular Microbiology, NIAID, NIH, Bethesda, MD
New England Primate Research Center, Southborough, MA
Department of Pathology, University of Pennsylvania, Philadelphia, PA

* Corresponding author; email: ipandrea{at}tulane.edu.

In contrast to lentiviral infections of humans and macaques, SIV infection of natural hosts is non-pathogenic 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. As this immunological feature is found in five different species of natural SIV hosts (sooty mangabeys, African green monkeys, mandrills, sun-tailed monkeys, and chimpanzes) but absent in four non-natural/recent hosts (humans, rhesus, pigtail, cynomolgous macaques, and baboons), it may represent a key feature of the co-evolution between the virus and its natural hosts that led to a non-pathogenic infection. Beneficial effects of low CCR5 expression on CD4+ T-cells may include the reduction of target cells for viral replication and/or a decreased homing of activated CD4+ T-cells to inflamed tissue.


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