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Journal of Virology, July 2008, p. 6767-6771, Vol. 82, No. 13
0022-538X/08/$08.00+0 doi:10.1128/JVI.02550-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Clinical Sciences Division, University of Toronto, Toronto, Canada,1 St. Michael's Hospital, University of Toronto, Toronto, Canada,3 CIRC (Canadian Immunodeficiency Research Collaborative), Toronto, Canada2
Received 28 November 2007/ Accepted 11 April 2008
TH-17 cells have been shown to play a role in bacterial defense, acute inflammation, and autoimmunity. We examined the role of interleukin 17 (IL-17) production in human immunodeficiency virus type 1 (HIV-1) infection. Both HIV-1- and cytomegalovirus (CMV)-specific IL-17-producing CD4+ T cells were detectable in early HIV-1 infection but were reduced to nondetectable levels in chronic and nonprogressive HIV-1 infection. IL-17-producing CMV-specific cells were not detected in blood from HIV-1-uninfected normal volunteers. Virus-specific TH-17 cells could coexpress other cytokines and could express CCR4 or CXCR3. Although the etiology of these cells has yet to be established, we propose that microbial translocation may induce them.
Published ahead of print on 23 April 2008.
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