4.5 Article

Booster dose after 10 years is recommended following 17DD-YF primary vaccination

期刊

HUMAN VACCINES & IMMUNOTHERAPEUTICS
卷 12, 期 2, 页码 491-502

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/21645515.2015.1082693

关键词

yellow fever; vaccine; cytokine; flow cytometry; memory cells and vaccination; duration of immunity

资金

  1. Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG)
  2. Bio-Manguinhos/FIOCRUZ
  3. PROEP/CPqRR/FIOCRUZ
  4. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  5. Programa Nacional de Imunizacoes (PNI) - Ministerio da Saude Brazil
  6. FIOTEC
  7. PDTIS
  8. CAPES
  9. Secretaria de Vigilancia em Saude (SVS)
  10. CNPq MCTI/CNPQ/Universal [14/2014, 444417/2014-1, 458134/2014-7]
  11. CNPq

向作者/读者索取更多资源

A single vaccination of Yellow Fever vaccines is believed to confer life-long protection. In this study, results of vaccinees who received a single dose of 17DD-YF immunization followed over 10 y challenge this premise. YF-neutralizing antibodies, subsets of memory T and B cells as well as cytokine-producing lymphocytes were evaluated in groups of adults before (NVday0) and after (PVday30-45, PVyear1-4, PVyear5-9, PVyear10-11, PVyear12-13) 17DD-YF primary vaccination. YF-neutralizing antibodies decrease significantly from PVyear1-4 to PVyear12-13 as compared to PVday30-45, and the seropositivity rates (PRNT2.9Log(10)mIU/mL) become critical (lower than 90%) beyond PVyear5-9. YF-specific memory phenotypes (effector T-cells and classical B-cells) significantly increase at PVday30-45 as compared to naive baseline. Moreover, these phenotypes tend to decrease at PVyear10-11 as compared to PVday30-45. Decreasing levels of TNF-(+) and IFN-(+) produced by CD4(+) and CD8(+) T-cells along with increasing levels of IL-10(+)CD4(+)T-cells were characteristic of anti-YF response over time. Systems biology profiling represented by hierarchic networks revealed that while the naive baseline is characterized by independent micro-nets, primary vaccinees displayed an imbricate network with essential role of central and effector CD8(+) memory T-cell responses. Any putative limitations of this cross-sectional study will certainly be answered by the ongoing longitudinal population-based investigation. Overall, our data support the current Brazilian national immunization policy guidelines that recommend one booster dose 10 y after primary 17DD-YF vaccination.

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