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Dendritic Cell Numbers in the Blood of HIV-1 Infected Patients Before and After Changes in Antiretroviral Therapy
Authors:JENNIFER?S.?FINKE,MICHAEL?SHODELL,KOKILA?SHAH,FREDERICK?P.?SIEGAL,RALPH?M.?STEINMAN  author-information"  >  author-information__contact u-icon-before"  >  mailto:steinma@mail.rockefeller.edu"   title="  steinma@mail.rockefeller.edu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York, NY, 10021;(2) Comprehensive HIV Center, Saint Vincent"rsquo"s Hospital and Medical Center, New York, NY, 10011
Abstract:Antigen presenting dendritic cells (DCs) can serve as sites for HIV replication and as vehicles for transmission of the virus to T cells. It is known that the numbers of DCs in blood is reduced during HIV-1 infection. Here we monitored the two major subsets of blood DCs in 12 individuals undergoing a change, primarily initiation, of highly active antiretroviral therapy. The numbers of plasmacytoid DCs were reliably higher on therapy, although in the 1–3 month interval we followed, these numbers did not return to those seen in HIV uninfected controls. An increase in plasmacytoid DCs was accompanied by an increase in IFN-agr production in response to a standard challenge in culture with UV-inactivated herpes simplex virus. The levels of myeloid DCs also demonstrated an increase while on HAART, and these numbers become comparable to the HIV uninfected controls. The numbers of plasmacytoid and myeloid DCs varied inversely with the levels of plasma HIV viremia. These longitudinal studies extend prior work showing that virus infection with HIV leads to a decrease in the number of dendritic cells in blood, and that this can be reversed at least in part by therapy.
Keywords:Plasmacytoid dendritic cells  myeloid dendritic cells  IFN-  /content/m4677852536825g2/xxlarge945.gif"   alt="  agr"   align="  BASELINE"   BORDER="  0"  > production  HIV-1 infection and HAART
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