Effect of cytomegalovirus-induced immune response, self antigen-induced immune response, and microbial translocation on chronic immune activation in successfully treated HIV type 1-infected patients: the ANRS CO3 Aquitaine Cohort.

Abstract : We evaluated the impact of cytomegalovirus (CMV)-induced immune responses, autoimmune-induced immune responses, and microbial translocation on immune activation in 191 human immunodeficiency virus type 1-infected patients from the ANRS CO3 Aquitaine Cohort. All enrolled subjects had achieved long-term virological suppression during receipt of combination antiretroviral therapy (cART). HLA-DR(+)/CD38(+) expression was 16.8% among CD8(+) T cells. Independent of age, CD4(+) T-cell count, 16S ribosomal DNA load, and regulatory T-cell count, positive results of Quantiferon CMV analysis (P = .02), positive results of CMV-pp65 enzyme-linked immunosorbent spot analysis (P = .01), positive results of CMV-pp65-specific CD8(+) T-cell analysis (P = .05), and CMV seropositivity (P = .01) were associated with a higher percentage of CD8+ T cells that expressed HLA-DR+/CD38+. Autoimmune response and microbial translocation were not associated with immune activation. Therefore, the CMV-induced immune response seems to be associated with chronic immune activation in cART recipients with sustained virological suppression.
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Journal of Infectious Diseases, Oxford University Press (OUP), 2013, 207 (4), pp.622-7. 〈10.1093/infdis/jis732.〉
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Contributeur : Linda Wittkop <>
Soumis le : dimanche 26 janvier 2014 - 13:05:46
Dernière modification le : jeudi 11 janvier 2018 - 06:21:10

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Linda Wittkop, Juliette Bitard, Estibaliz Lazaro, Didier Neau, Fabrice Bonnet, et al.. Effect of cytomegalovirus-induced immune response, self antigen-induced immune response, and microbial translocation on chronic immune activation in successfully treated HIV type 1-infected patients: the ANRS CO3 Aquitaine Cohort.. Journal of Infectious Diseases, Oxford University Press (OUP), 2013, 207 (4), pp.622-7. 〈10.1093/infdis/jis732.〉. 〈inserm-00936482〉

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