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Activated dendritic cells and monocytes in HIV immunological nonresponders: HIV-induced interferon-inducible protein-10 correlates with low future CD4(+) recovery

OBJECTIVE: To explore monocyte and dendritic cell immune responses, and their association with future CD4(+) gain in treated HIV patients with suboptimal CD4(+) recovery. DESIGN: A cross-sectional study of HIV-infected, virally suppressed individuals on antiretroviral therapy for at least 24 months;...

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Detalles Bibliográficos
Autores principales: Stiksrud, Birgitte, Aass, Hans C.D., Lorvik, Kristina B., Ueland, Thor, Trøseid, Marius, Dyrhol-Riise, Anne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511429/
https://www.ncbi.nlm.nih.gov/pubmed/30789356
http://dx.doi.org/10.1097/QAD.0000000000002173
Descripción
Sumario:OBJECTIVE: To explore monocyte and dendritic cell immune responses, and their association with future CD4(+) gain in treated HIV patients with suboptimal CD4(+) recovery. DESIGN: A cross-sectional study of HIV-infected, virally suppressed individuals on antiretroviral therapy for at least 24 months; 41 immunological nonresponders (INRs) (CD4(+) cell count <400 cells/μl) and 26 immunological responders (CD4(+) cell count >600 cells/μl). Ten HIV-infected antiretroviral therapy-naive and 10 HIV-negative healthy persons served as controls. CD4(+) cell counts were registered after median 2.4 and 4.7 years. METHODS: Monocyte, dendritic-cell and T-cell activation and regulatory T cells (Tregs) were analyzed by flow cytometry. In INR and immunological responder subgroups matched on age and nadir CD4(+) cell count, upregulation of interferon-inducible protein-10 (IP-10) and indoleamine 2,3-dioxygenase in monocytes and dendritic cells and cytokines in cell supernatants were measured in vitro in peripheral blood mononuclear cells stimulated with aldrithiol-2-inactivated HIV-1. RESULTS: The INR group displayed higher spontaneous activation of both monocytes (HLA-DR(+)) and myeloid and plasmacytoid dendritic cells (HLA-DR(+), CD83(+) and CD86(+)) compared with immunological responders, and this was associated with increased T-cell activation (CD38(+)HLA-DR(+)), an effector memory T-cell phenotype and activated Tregs. The IP-10 response in monocytes after in-vitro HIV stimulation was negatively associated with prospective CD4(+) gain. IP-10, indoleamine 2,3-dioxygenase and cytokines levels were comparable between the groups, but inversely correlated with activated Tregs in INRs. CONCLUSION: HIV-infected individuals with suboptimal immune recovery demonstrated more activated monocytes and in particular dendritic cells, compared with patients with acceptable CD4(+) gain. A high level of HIV-specific IP-10 expression in monocytes may be predictive of future CD4(+) recovery.