Varicella-zoster virus-specific immune responses in elderly recipients of a herpes zoster vaccine

  • Myron J. Levin
  • , M. N. Oxman
  • , J. H. Zhang
  • , G. R. Johnson
  • , H. Stanley
  • , A. R. Hayward
  • , M. J. Caulfield
  • , M. R. Irwin
  • , J. G. Smith
  • , J. Clair
  • , I. S.F. Chan
  • , H. Williams
  • , R. Harbecke
  • , R. Marchese
  • , S. E. Straus
  • , A. Gershon
  • , A. Weinberg
  • , Michael N. Oxman
  • , Robert Arbeit
  • , Patricia Barry
  • Chris Beisel, Kathy D. Boardman, Cindy L. Colling, Larry Davis, Lawrence Gelb, Anne A. Gershon, Anthony R. Hayward, Gary R. Johnson, Peter N. Peduzzi, Kenneth Schmader, Michael S. Simberkoff, Stephen E. Straus, Adriana Weinberg, Heather M. Williams, Jeffrey L. Silber, Paula Annunziato, Christina Y. Chan, Ivan S.F. Chan, L. E. Davis, C. A. Kauffman, S. K. Keay, A. R. Marques, 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, K. M. Neuzil, J. F. Toney

Research output: Contribution to journalArticlepeer-review

335 Scopus citations

Abstract

Background. A double-blind, placebo-controlled trial that involved 38,546 subjects ≥60 years old demonstrated efficacy of a high-potency live-attenuated Oka/Merck varicella-zoster virus (VZV) vaccine. The trial included an immunology substudy to determine the relationship of VZV-specific immune responses to vaccination and clinical outcome. Methods. The immunology substudy enrolled 1395 subjects at 2 sites where blood samples obtained prior to vaccination, at 6 weeks after vaccination, and at 1, 2, and 3 years thereafter were tested for VZV-specific cell-mediated immunity (VZV-CMI) by γ-interferon ELISPOT and responder cell frequency assays and for VZV antibody by glycoprotein ELISA. Results. VZV-CMI and VZV antibodies were significantly increased in vaccine recipients at 6 weeks after vaccination. The vaccine-induced increases in VZV-CMI persisted during the 3 years of follow-up, although their magnitude decreased over time. The magnitude of these VZV-specific immune responses was greater in subjects 60-69 years old than in subjects ≥70 years old. Conclusions. The zoster vaccine induced a significant increase in VZV-CMI and VZV antibody. The magnitude and duration of the boost in VZV-CMI in vaccine recipients and the relationship of this boost to age paralleled the clinical effects of the vaccine observed during the efficacy trial. These findings support the hypothesis that boosting VZV-CMI protects older adults against herpes zoster and postherpetic neuralgia.

Original languageEnglish
Pages (from-to)825-835
Number of pages11
JournalJournal of Infectious Diseases
Volume197
Issue number6
DOIs
StatePublished - Mar 15 2008

Bibliographical note

Funding Information:
Financial support: National Institute of Child Health and Human Development (grant contract N01-HD-3–3345 to M.J.L.); Health Resources and Services Administration (H12HA00070 and NIAID U01 AI068632 to M.J.L.); Cousins Center for Psychoneuroimmunology (grant to M.R.I.); NHLBI (grant R01 HL079955 to M.R.I.); NIA (grants R01 AG026364 and R01 AG026006–01 to M.R.I.); NCF (grant R01 CA 10014152 to M.R.I.); NIMH (grant T32MH19925 to M.R.I.); NIPS (grant P60 AG 10415 to M.R.I.); NCRR (grant M01-RR00865 to M.R.I.); and NIAMS (grants R01 NR009228 and R01 AR049840 to M.R.I.). Additional support was provided by the National Institute of Allergy and Infectious Diseases, Merck & Co., the National Institutes of Health (grant NIMH R01 MH 55253 to M.J.I.), and by the James R. and Jesse V. Scott Fund for Shingles Research (to M.N.O.). a Deceased.

Funding

Financial support: National Institute of Child Health and Human Development (grant contract N01-HD-3–3345 to M.J.L.); Health Resources and Services Administration (H12HA00070 and NIAID U01 AI068632 to M.J.L.); Cousins Center for Psychoneuroimmunology (grant to M.R.I.); NHLBI (grant R01 HL079955 to M.R.I.); NIA (grants R01 AG026364 and R01 AG026006–01 to M.R.I.); NCF (grant R01 CA 10014152 to M.R.I.); NIMH (grant T32MH19925 to M.R.I.); NIPS (grant P60 AG 10415 to M.R.I.); NCRR (grant M01-RR00865 to M.R.I.); and NIAMS (grants R01 NR009228 and R01 AR049840 to M.R.I.). Additional support was provided by the National Institute of Allergy and Infectious Diseases, Merck & Co., the National Institutes of Health (grant NIMH R01 MH 55253 to M.J.I.), and by the James R. and Jesse V. Scott Fund for Shingles Research (to M.N.O.). a Deceased.

FundersFunder number
James R. and Jesse V. Scott Fund for Shingles Research
National Institutes of Health (NIH)R01 MH 55253
National Institute of Mental HealthT32MH19925
National Institute on AgingR01 AG026006–01, R01 AG026364
National Heart, Lung, and Blood Institute (NHLBI)R01 HL079955
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...U01 AI068632
National Institute of Arthritis and Musculoskeletal and Skin DiseasesR01 NR009228, R01AR049840
NIH National Institute of Child Health and Human Development National Center for Medical Rehabilitation ResearchN01-HD-3–3345
National Center for Research ResourcesM01-RR00865
Health Resources and Services AdministrationH12HA00070
Nathan Cummings FoundationR01 CA 10014152
Merck
Norman Cousins Center for Psychoneuroimmunology
National Institutes of Natural Sciences, National Institute for Physiological SciencesP60 AG 10415

    ASJC Scopus subject areas

    • Immunology and Allergy
    • Infectious Diseases

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