Comparison between HIV- and CMV-specific T cell responses in long-term HIV infected donors

Laura Papagno(John Radcliffe Hospital), Victor Appay(John Radcliffe Hospital), John Sutton(John Radcliffe Hospital), Tim Rostron(John Radcliffe Hospital), Geraldine M. Gillespie(John Radcliffe Hospital), Graham S. Ogg(John Radcliffe Hospital), Abigail King(John Radcliffe Hospital), A T MAKADZANHGE(John Radcliffe Hospital), A. Waters, Claudia Balotta(Luigi Sacco Hospital), Annapurna Vyakarnam, Philippa Easterbrook, Sarah Rowland‐Jones(John Radcliffe Hospital)
Clinical & Experimental Immunology
November 24, 2002
Cited by 56Open Access
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Abstract

The mechanisms underlying non-progression in HIV-1 infection are not well understood; however, this state has been associated previously with strong HIV-1-specific CD8+ T cell responses and the preservation of proliferative CD4+ T cell responses to HIV-1 antigens. Using a combination of interferon-gamma (IFN-gamma) ELISpot assays and tetramer staining, the HIV-1-specific CD8+ T cell populations were quantified and characterized in untreated long-term HIV-1-infected non-progressors and individuals with slowly progressive disease, both in relation to CD4+ T cell responses, and in comparison with responses to cytomegalovirus (CMV) antigens. High levels of CD8+ T cell responses specific for HIV-1 or CMV were observed, but neither their frequency nor their phenotype seemed to differ between the two patient groups. Moreover, while CMV-specific CD4+ T cell responses were preserved in these donors, IFN-gamma release by HIV-1-specific CD4+ T cells was generally low. These data raise questions with regard to the role played by CD8+ T cells in the establishment and maintenance of long-term non-progression.


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