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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Antibodies are not required to a protective immune response against dengue virus elicited in a mouse encephalitis model

Texto completo
Autor(es):
Amorim, Jaime Henrique [1] ; dos Santos Alves, Rubens Prince [1] ; Bizerra, Raiza [1] ; Pereira, Sara Araujo [1] ; Pereira, Lennon Ramos [1] ; Nascimento Fabris, Denicar Lina [1] ; Santos, Robert Andreata [1] ; Romano, Camila Malta [2, 3] ; de Souza Ferreira, Luis Carlos [1]
Número total de Autores: 9
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Dept Microbiol, Lab Desenvolvimento Vacinas, BR-05508000 Sao Paulo, SP - Brazil
[2] Univ Sao Paulo, Fac Med, BR-05508000 Sao Paulo, SP - Brazil
[3] Univ Sao Paulo, Dept Mol Infecciosas & Parasitarias LIMHC, Inst Med Trop Sao Paulo, BR-05508000 Sao Paulo, SP - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: VIROLOGY; v. 487, p. 41-49, JAN 2016.
Citações Web of Science: 8
Resumo

Generating neutralizing antibodies have been considered a prerequisite to control dengue virus (DENV) infection. However, T lymphocytes have also been shown to be important in a protective immune state. In order to investigate the contribution of both humoral and cellular immune responses in DENV immunity, we used an experimental model in which a non-lethal DENV2 strain (ACS46) is used to intracranially prime Balb/C mice which develop protective immunity against a lethal DENV2 strain (JHA1). Primed mice generated envelope-specific antibodies and CD8(+) T cell responses targeting mainly non-structural proteins. Immune sera from protected mice did not confer passive protection to naive mice challenged with the JHA1 strain. In contrast, depletion of CD4(+) and CD8(+) T lymphocytes significantly reduced survival of ACS46-primed mice challenged with the JHA1 strain. Collectively, results presented in this study show that a cellular immune response targeting non-structural proteins are a promising way in vaccine development against dengue. (C) 2015 Elsevier Inc. All rights reserved. (AU)

Processo FAPESP: 12/51204-2 - Um novo caminho para a busca racional de uma vacina efetiva contra a dengue
Beneficiário:Jaime Henrique Amorim Santos
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado