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Journal of Virology, December 2007, p. 13456-13468, Vol. 81, No. 24
0022-538X/07/$08.00+0 doi:10.1128/JVI.01619-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

CEA, Service d'Immuno-Virologie, DSV/iMETI, IPSC, Fontenay-aux-Roses, France,1 Université Paris XI, UMRE01, Orsay, France2
Received 25 July 2007/ Accepted 26 September 2007
Cellular immune responses make an important contribution to both the control of human immunodeficiency virus (HIV) replication and disease progression. We used a pathogenic model of SIVmac251 infection of cynomolgus macaques to longitudinally evaluate cellular immune responses in association with various rates of disease progression. We found an inverse relationship between plasma viral load and the simian immunodeficiency virus (SIV)-specific T cells responses in peripheral blood and lymph nodes. SIV-specific T-cell responses in peripheral blood were transient during primary infection, with the highest responses detected around 3 months after infection. There was also a transient increase of central memory CD8+ T cells in peripheral blood during primary infection, and effector memory T-cell counts in peripheral lymph nodes were increased. This study emphasizes the importance of the early virus-specific immune responses in the outcome of HIV/SIV disease and provides details about the changes of virus-specific immune responses over time.
Published ahead of print on 3 October 2007.
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