Effect of Maraviroc intensification on HIV-1-specific T cell immunity in recently HIV-1-infected individuals

BACKGROUND: The effect of maraviroc on the maintenance and the function of HIV-1-specific T cell responses remains unknown. METHODS: Subjects recently infected with HIV-1 were randomized to receive anti-retroviral treatment with or without maraviroc intensification for 48 weeks, and were monitored u...

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Detalles Bibliográficos
Autores: Kawana-Tachikawa, Ai, Llibre, Josep María, Bravo, Isabel, Escrig, Roser, Mothe, Beatriz, Puig, Jordi, Puertas Castro, Ma. Carmen, Martínez Picado, Francisco Javier, Blanco, Julià, Manzardo, Christian, Miró Meda, José M. (José María), 1956-, Iwamoto, Aikichi, Pozniak, Anton L., Gatell, José M., Clotet, Bonaventura, 1953-, Brander, Christian
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2014
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/109602
Acceso en línea:https://hdl.handle.net/2445/109602
Access Level:acceso abierto
Palabra clave:Cèl·lules T
VIH (Virus)
Antiretrovirals
Resposta immunitària
Genètica molecular
T cells
HIV (Viruses)
Antiretroviral agents
Immune response
Molecular genetics
Descripción
Sumario:BACKGROUND: The effect of maraviroc on the maintenance and the function of HIV-1-specific T cell responses remains unknown. METHODS: Subjects recently infected with HIV-1 were randomized to receive anti-retroviral treatment with or without maraviroc intensification for 48 weeks, and were monitored up to week 60. PBMC and in vitro-expanded T cells were tested for responses to the entire HIV proteome by ELISpot analyses. Intracellular cytokine staining assays were conducted to monitor the (poly)-functionality of HIV-1-specific T cells. Analyses were performed at baseline and week 24 after treatment start, and at week 60 (3 months after maraviroc discontinuation). RESULTS: Maraviroc intensification was associated with a slower decay of virus-specific T cell responses over time compared to the non-intensified regimen in both direct ex-vivo as well as in in-vitro expanded cells. The effector function profiles of virus-specific CD8⁺ T cells were indistinguishable between the two arms and did not change over time between the groups. CONCLUSIONS: Maraviroc did not negatively impact any of the measured parameters, but was rather associated with a prolonged maintenance of HIV-1-specific T cell responses. Maraviroc, in addition to its original effect as viral entry inhibitor, may provide an additional benefit on the maintenance of virus-specific T cells which may be especially important for future viral eradication strategies.