Immune Reconstitution and Viral Stimulation Are Required to Restore HIV-Specific CD8 T Cell Responses Following Advanced Infection
Identifieur interne : 001167 ( Istex/Curation ); précédent : 001166; suivant : 001168Immune Reconstitution and Viral Stimulation Are Required to Restore HIV-Specific CD8 T Cell Responses Following Advanced Infection
Auteurs : Jane Gamberg [Canada] ; Lisa Barrett [Canada] ; Ian Bowmer [Canada] ; Constance Howley [Canada] ; Michael Grant [Canada]Source :
- Journal of Clinical Immunology [ 0271-9142 ] ; 2004-03-01.
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Abstract
Abstract: The extent to which highly active antiretroviral therapy (HAART) restores human immunodeficiency virus (HIV)-specific immunity in advanced infection is unknown. Therefore, we studied how effective therapy affected HIV-specific CD8+ T cell responses in 4 individuals who had progressed to advanced infection. CD8+ T cell responses were assessed by cytotoxicity and interferon-gamma (IFN-γ) production. Proliferative CD4+ T cell responses against HIV, Candida and mitogen were measured by 3H-thymidine incorporation. Substantial immune reconstitution indicated by increased CD4+ and CD8+ T cell numbers followed suppression of viral replication. This was associated with emergence of HIV-specific cytotoxic T lymphocytes (CTL), but only concurrent with detectable viral replication. Emergent anti-HIV CTL were similar to those at earlier stages of infection in terms of their specificity, function, and CD28 phenotype. However, they were very short-lived in the absence of detectable HIV replication. Antigen-specific CD4+ T cell responses remained severely compromised. Thus, effective antiretroviral therapy restores the capacity for HIV-specific CTL responses after advanced infection. However, the transient nature of these responses suggests failure to generate stable long-lived memory cells in the absence of HIV-specific helper T cell responses.
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DOI: 10.1023/B:JOCI.0000019776.38147.e6
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in advanced infection is unknown. Therefore, we studied how effective therapy affected HIV-specific CD8+ T cell responses in 4 individuals who had progressed to advanced infection. CD8+ T cell responses were assessed by cytotoxicity and interferon-gamma (IFN-γ) production. Proliferative CD4+ T cell responses against HIV, Candida and mitogen were measured by 3H-thymidine incorporation. Substantial immune reconstitution indicated by increased CD4+ and CD8+ T cell numbers followed suppression of viral replication. This was associated with emergence of HIV-specific cytotoxic T lymphocytes (CTL), but only concurrent with detectable viral replication. Emergent anti-HIV CTL were similar to those at earlier stages of infection in terms of their specificity, function, and CD28 phenotype. However, they were very short-lived in the absence of detectable HIV replication. Antigen-specific CD4+ T cell responses remained severely compromised. 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