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Journal of Virology, March 2009, p. 2778-2782, Vol. 83, No. 6
0022-538X/09/$08.00+0 doi:10.1128/JVI.01420-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Centre de Recherche en Infectiologie,1 Centre de Recherche en Rhumatologie et Immunologie,2 Centre Hospitalier de l'Université Laval, and Département de Biologie Médicale, Faculté de Médecine, Université Laval, Québec, Canada3
Received 8 July 2008/ Accepted 19 December 2008
Dendritic cells (DC) are considered to be important contributors to human immunodeficiency virus type 1 (HIV-1) transmission and pathogenesis. As the first target cells in mucosal tissues, they can be become productively infected and can also capture virions and transfer them efficiently to CD4+ T cells located within lymphoid tissues. Resting CD4+ T cells appear to be another major target of HIV-1 in vivo, yet several blocks restrict replication in such cells. We report here that physical contact between virus-infected quiescent CD4+ T cells and uninfected autologous immature DC in the absence of any foreign antigen relieves these restrictions, allowing a highly productive HIV-1 replication.
Published ahead of print on 24 December 2008.
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