| Literature DB >> 16730772 |
Nataliya Trunova1, Lily Tsai, Stephanie Tung, Eric Schneider, Janet Harouse, Agegnehu Gettie, Viviana Simon, James Blanchard, Cecilia Cheng-Mayer.
Abstract
Nine rhesus macaques in groups of three received a single dose of the injectable progestin-based contraceptive Depo-Provera 5 weeks prior to challenge intravaginally with varying doses of a mixture of the pathogenic CXCR4 (X4)-SHIV(SF33A) and CCR5 (R5)-SHIV(SF162P3) isolates. As controls, seven Depo-naive animals were inoculated once with a high-dose of the mixed inoculum. Irrespective of inoculum dose, acute viremia was higher in the Depo-treated than in the Depo-naive animals. Further, genetic complexity of the replicating virus was greater and replication of the X4 virus was favored in dually infected animals treated with Depo-Provera. Analysis of cellular immune responses revealed slower response rates in virus-specific IFN-gamma production to SIV Gag in the Depo-treated macaques. The immunosuppressive effect of Depo-Provera on mounting an antiviral cellular immune response may account for the increase viral burden and diversity, and the predominance of X4 virus replication in SHIV infected macaques that were administered the progestin-based contraceptive.Entities:
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Year: 2006 PMID: 16730772 DOI: 10.1016/j.virol.2006.04.004
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616