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17DD Yellow Fever Revaccination and Heightened Long-Term Immunity in Populations of Disease-Endemic Areas, Brazil

We evaluated the duration of neutralizing antibodies and the status of 17DD vaccine–specific T- and B-cell memory following primary and revaccination regimens for yellow fever (YF) in Brazil. We observed progressive decline of plaque-reduction neutralization test (PRNT) seropositivity and of the lev...

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Detalles Bibliográficos
Autores principales: Campi-Azevedo, Ana Carolina, Peruhype-Magalhāes, Vanessa, Coelho-dos-Reis, Jordana Grazziela, Antonelli, Lis Ribeiro, Costa-Pereira, Christiane, Speziali, Elaine, Reis, Laise Rodrigues, Lemos, Jandira Aparecida, Ribeiro, José Geraldo Leite, Bastos Camacho, Luiz Antônio, de Sousa Maia, Maria de Lourdes, Barbosa de Lima, Sheila Maria, Simões, Marisol, de Menezes Martins, Reinaldo, Homma, Akira, Cota Malaquias, Luiz Cosme, Tauil, Pedro Luiz, Costa Vasconcelos, Pedro Fernando, Martins Romano, Alessandro Pecego, Domingues, Carla Magda, Teixeira-Carvalho, Andréa, Martins-Filho, Olindo Assis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649311/
https://www.ncbi.nlm.nih.gov/pubmed/31298654
http://dx.doi.org/10.3201/eid2508.181432
Descripción
Sumario:We evaluated the duration of neutralizing antibodies and the status of 17DD vaccine–specific T- and B-cell memory following primary and revaccination regimens for yellow fever (YF) in Brazil. We observed progressive decline of plaque-reduction neutralization test (PRNT) seropositivity and of the levels of effector memory CD4+ and CD8+ T cells, as well as interferon-γ+CD8+ T cells, 10 years after primary vaccination. Revaccination restored PRNT seropositivity as well as the levels of effector memory CD4+, CD8+, and interferon-γ+CD8+ T cells. Moreover, secondary or multiple vaccinations guarantee long-term persistence of PRNT positivity and cell-mediated memory 10 years after booster vaccination. These findings support the relevance of booster doses to heighten the 17DD-YF–specific immune response to guarantee the long-term persistence of memory components. Secondary or multiple vaccinations improved the correlates of protection triggered by 17DD-YF primary vaccination, indicating that booster regimens are needed to achieve efficient immunity in areas with high risk for virus transmission.