Your browser doesn't support javascript.
loading
Low antibody titers 5 years after vaccination with the CYD-TDV dengue vaccine in both pre-immune and naïve vaccinees.
Velumani, Sumathy; Toh, Ying Xiu; Balasingam, Shobana; Archuleta, Sophia; Leo, Yee Sin; Gan, Victor C; Thein, Tun Linn; Wilder-Smith, Annelies; Fink, Katja.
Afiliação
  • Velumani S; a Singapore Immunology Network, Agency for Science, Technology (A*STAR) , Singapore , Singapore.
  • Toh YX; a Singapore Immunology Network, Agency for Science, Technology (A*STAR) , Singapore , Singapore.
  • Balasingam S; b Lee Kong Chian School of Medicine, Nanyang Technological University , Singapore , Singapore.
  • Archuleta S; c Division of Infectious Diseases, University Medicine Cluster, National University Hospital , Singapore , Singapore.
  • Leo YS; d Department of Medicine , Yong Loo Lin School of Medicine, National University of Singapore , Singapore.
  • Gan VC; e Communicable Disease Center, Institute of Infectious Disease and Epidemiology, Tan Tock Seng Hospital , Singapore , Singapore.
  • Thein TL; f Yong Loo Lin School of Medicine, National University of Singapore , Singapore , Singapore.
  • Wilder-Smith A; e Communicable Disease Center, Institute of Infectious Disease and Epidemiology, Tan Tock Seng Hospital , Singapore , Singapore.
  • Fink K; e Communicable Disease Center, Institute of Infectious Disease and Epidemiology, Tan Tock Seng Hospital , Singapore , Singapore.
Hum Vaccin Immunother ; 12(5): 1265-73, 2016 05 03.
Article em En | MEDLINE | ID: mdl-26889737
Globally, dengue virus (DENV) is one of the most widespread vector-borne viruses. Dengue disease affects populations in endemic areas and, increasingly, tourists who travel to these countries, but there is currently no approved vaccine for dengue. A phase 3 efficacy trial with Sanofi-Pasteur's recombinant, live-attenuated, tetravalent dengue vaccine (CYD-TDV) conducted in South East Asia showed an overall efficacy of 56% against virologically confirmed dengue infections of any severity and any of the 4 serotypes, but the long-term protection of the vaccine has yet to be demonstrated. To address longevity of antibody titers and B cell memory, we recalled study participants from an earlier CYD immunogenicity study (Phase 2) conducted in Singapore that enrolled healthy volunteers in the year 2009. Depending on the age group, 57-84% of the participants initially generated a neutralizing antibody titer ≥ 10 to all 4 DENV serotypes 28 d after the third and final dose. We observed very low antibody titers in blood samples collected from 23 vaccinees 5 y after the first dose, particularly titers of antibodies binding to virus particles compared with those binding to recombinant E protein. The in vivo efficacy of plasma antibodies against DENV-2 challenge was also tested in a mouse model, which found that only 2 out of 23 samples were able to reduce viremia. Although the sample size is too small for general conclusions, dengue immune memory after vaccination with CYD-TDV appears relatively low.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus da Dengue / Vacinas contra Dengue / Anticorpos Neutralizantes / Memória Imunológica / Anticorpos Antivirais Tipo de estudo: Prognostic_studies Limite: Adult / Animals / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Hum Vaccin Immunother Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Singapura

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus da Dengue / Vacinas contra Dengue / Anticorpos Neutralizantes / Memória Imunológica / Anticorpos Antivirais Tipo de estudo: Prognostic_studies Limite: Adult / Animals / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Hum Vaccin Immunother Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Singapura