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Long-term persistence of zoster vaccine efficacy

  • Vicki A. Morrison
  • , Gary R. Johnson
  • , Kenneth E. Schmader
  • , Myron J. Levin
  • , Jane H. Zhang
  • , David J. Looney
  • , Robert Betts
  • , Larry Gelb
  • , John C. Guatelli
  • , Ruth Harbecke
  • , Connie Pachucki
  • , Susan Keay
  • , Barbara Menzies
  • , Marie R. Griffin
  • , Carol A. Kauffman
  • , Adriana Marques
  • , John Toney
  • , Kathy Boardman
  • , Shu Chih Su
  • , Xiaoming Li
  • Ivan S.F. Chan, Janie Parrino, Paula Annunziato, Michael N. Oxman, L. E. Davis, C. A. Kauffman, S. K. Keay, S. E. Straus, N. E. Soto, P. Brunell, J. W. Gnann, R. Serrao, D. J. Cotton, R. P. Goodman, R. D. Arbeit, C. T. Pachucki, M. J. Levin, K. E. Schmader, W. A. Keitel, R. N. Greenberg, V. A. Morrison, P. F. Wright, M. R. Griffin, M. S. Simberkoff, S. S. Yeh, Z. Lobo, M. Holodniy, J. Loutit, R. F. Betts, L. D. Gelb, G. E. Crawford, J. Guatelli, P. A. Brooks, D. J. Looney, K. M. Neuzil, J. F. Toney, C. A. Kauffman, S. K. Keay, C. T. Pachucki, M. J. Levin, K. E. Schmader, V. A. Morrison, P. F. Wright, M. R. Griffin, R. F. Betts, L. D. Gelb, J. Guatelli, D. J. Looney, K. M. Neuzil, B. Menzies, J. F. Toney

Producción científica: Articlerevisión exhaustiva

286 Citas (Scopus)

Resumen

Background. The Shingles Prevention Study (SPS) demonstrated zoster vaccine efficacy through 4 years postvaccination. A Short-Term Persistence Substudy (STPS) demonstrated persistence of vaccine efficacy for at least 5 years. A Long-Term Persistence Substudy (LTPS) was undertaken to further assess vaccine efficacy in SPS vaccine recipients followed for up to 11 years postvaccination. Study outcomes were assessed for the entire LTPS period and for each year from 7 to 11 years postvaccination. Methods. Surveillance, case determination, and follow-up were comparable to those in SPS and STPS. Because SPS placebo recipients were offered zoster vaccine before the LTPS began, there were no unvaccinated controls. Instead, SPS and STPS placebo results were used to model reference placebo groups. Results. The LTPS enrolled 6867 SPS vaccine recipients. Compared to SPS, estimated vaccine efficacy in LTPS decreased from 61.1% to 37.3% for the herpes zoster (HZ) burden of illness (BOI), from 66.5% to 35.4% for incidence of postherpetic neuralgia, and from 51.3% to 21.1% for incidence of HZ, and declined for all 3 outcome measures from 7 through 11 years postvaccination. Vaccine efficacy for the HZ BOI was significantly greater than zero through year 10 postvaccination, whereas vaccine efficacy for incidence of HZ was significantly greater than zero only through year 8. Conclusions. Estimates of vaccine efficacy decreased over time in the LTPS population compared with modeled control estimates. Statistically significant vaccine efficacy for HZ BOI persisted into year 10 postvaccination, whereas statistically significant vaccine efficacy for incidence of HZ persisted only through year 8.

Idioma originalEnglish
Páginas (desde-hasta)900-909
Número de páginas10
PublicaciónClinical Infectious Diseases
Volumen60
N.º6
DOI
EstadoPublished - mar 15 2015

Nota bibliográfica

Funding Information:
Financial support. The study was conducted by the Cooperative Studies Program, Department of Veterans Affairs, Office of Research and Development through an agreement between Merck & Co, Inc, and the VA Connecticut Research and Education Foundation (VACREF) under which funding was provided to VACREF by Merck & Co. Additional support was provided by the James R. and Jesse V. Scott Fund for Shingles Research, and by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases, National Institutes of Health.

Financiación

Financial support. The study was conducted by the Cooperative Studies Program, Department of Veterans Affairs, Office of Research and Development through an agreement between Merck & Co, Inc, and the VA Connecticut Research and Education Foundation (VACREF) under which funding was provided to VACREF by Merck & Co. Additional support was provided by the James R. and Jesse V. Scott Fund for Shingles Research, and by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases, National Institutes of Health.

FinanciadoresNúmero del financiador
James R. and Jesse V. Scott Fund for Shingles Research
VA Connecticut Research and Education Foundation
National Institutes of Health (NIH)
National Institute of Allergy and Infectious F32-AI286447 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R01AI168214 Jason W. Rosch Diseases National Institute of Allergy and Infectious P30 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R00-AI166116 Christopher D. Radka Diseases National Institute of Allergy and Infectious T32-AI106700 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R01AI192221 Jason W. Rosch Diseases National Inst...ZIAAI000856
U.S. Department of Veterans Affairs
Merck
Biomedical Laboratory Research and Development, VA Office of Research and Development

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Microbiology (medical)
    • Infectious Diseases

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