Old age and anti-cytomegalovirus immunity are associated with altered T-cell reconstitution in HIV-1-infected patients

Increasing evidence supports a parallel between HIV-1 infection and immune aging, which is particularly apparent with common changes in naive versus memory T-cell proportions. Here, we aimed at refining the value of common T-cell-associated markers of immunosenescence during HIV disease progression...

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Published inAIDS (London) Vol. 25; no. 15; pp. 1813 - 1822
Main Authors Appay, Victor, Fastenackels, Solène, Katlama, Christine, Ait-Mohand, Hocine, Schneider, Luminita, Guihot, Amélie, Keller, Michael, Grubeck-Loebenstein, Beatrix, Simon, Anne, Lambotte, Olivier, Hunt, Peter W., Deeks, Steven G., Costagliola, Dominique, Autran, Brigitte, Sauce, Delphine
Format Journal Article
LanguageEnglish
Published Hagerstown, MD Lippincott Williams & Wilkins 24.09.2011
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Summary:Increasing evidence supports a parallel between HIV-1 infection and immune aging, which is particularly apparent with common changes in naive versus memory T-cell proportions. Here, we aimed at refining the value of common T-cell-associated markers of immunosenescence during HIV disease progression or aging, and at exploring further the impact in this context of old age as well as cytomegalovirus (CMV) co-infection, which is predominant in HIV-1-infected individuals. Frequencies of naive or CD57(+) memory T cells as well as the magnitude of CMV-pp65 T cells were measured in HIV-1-infected patients grouped according to disease progression status, treatment and age. Our results indicate that the decline in naive T-cell levels rather than the accumulation of CD57(+) senescent T cells identifies best the premature development of an immunosenescence phenotype with HIV disease progression. Moreover, advanced age or mounting of strong CMV-specific responses impact independently on CD4(+) T-cell counts and recovery with antiretroviral therapy. The present findings indicate that HIV-1 infection amplifies the effect of age on naive T-cell levels, and highlight the constraint on the capacity of treated patients to reconstitute their CD4(+) T-cell compartment due to age and CMV co-infection.
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ISSN:0269-9370
1473-5571
1473-5571
DOI:10.1097/QAD.0b013e32834640e6