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We investigated whether vaccination of healthy HIV-seronegative and HIV-1-seropositive antiretroviral therapy-treated subjects with recombinant modified vaccinia virus Ankara expressing an HIV-1 immunogen (MVA.HIVA) induced MVA-specific T cell responses. Using IFN-γ Elispot assays, we observed new or increased responses to MVA virus in 52% of HIV-seronegative subjects and 93% HIV-1 seropositive subjects; MVA-specific T cell frequencies were generally low and correlated poorly with T cell responses to the HIV-1 immunogen. In two vaccinees, responses were mapped to CD8+ T cell epitopes present in replication-competent vaccinia virus. These data support further evaluation of MVA as a viral vector for HIV-1 immunogens.

Original publication

DOI

10.1016/j.vaccine.2010.08.077

Type

Journal article

Journal

Vaccine

Publication Date

10/2010

Volume

28

Pages

7306 - 7312

Addresses

MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford OX3 9DS, United Kingdom.

Keywords

T-Lymphocytes, Humans, Vaccinia virus, HIV-1, HIV Infections, AIDS Vaccines, Epitopes, T-Lymphocyte, Immunization, Secondary, Antiretroviral Therapy, Highly Active, HIV Seronegativity, Immunity, Cellular, Genetic Vectors, Adolescent, Adult, Middle Aged, Interferon-gamma, Young Adult