Varicella-zoster virus-specific immune responses to herpes zoster in elderly participants in a trial of a clinically effective zoster vaccine.

TitleVaricella-zoster virus-specific immune responses to herpes zoster in elderly participants in a trial of a clinically effective zoster vaccine.
Publication TypeJournal Article
Year of Publication2009
AuthorsWeinberg A, Zhang JH, Oxman MN, Johnson GR, Hayward AR, Caulfield MJ, Irwin MR, Clair J, Smith JG, Stanley H, Marchese RD, Harbecke R, Williams HM, Chan ISF, Arbeit RD, Gershon AA, Schödel F, Morrison VA, Kauffman CA, Straus SE, Schmader KE, Davis LE, Levin MJ
Corporate AuthorsUS Department of Veterans Affairs(VA) Cooperative Studies Program Shingles Prevention Study Investigators
JournalJ Infect Dis
Volume200
Issue7
Pagination1068-77
Date Published2009 Oct 1
ISSN0022-1899
KeywordsAged, Antibodies, Viral, Double-Blind Method, Female, Herpes Zoster, Herpesvirus 3, Human, Humans, Immunity, Cellular, Male, Middle Aged, Neuralgia, Postherpetic, Time Factors, Viral Vaccines
Abstract

BACKGROUND: The objectives of this study were to evaluate the association between varicella-zoster virus (VZV)-specific humoral and cell-mediated immunity (CMI) to herpes zoster (HZ) and protection against HZ morbidity and to compare immune responses to HZ and zoster vaccine.

METHODS: In 981 elderly persons who developed HZ during a zoster vaccine efficacy trial (321 vaccinees and 660 placebo recipients) and 1362 without HZ (682 vaccinees and 680 placebo recipients), CMI was measured by VZV responder cell frequency and interferon-gamma enzyme-linked immunospot, and antibodies were measured by VZV enzyme-linked immunosorbent assay against affinity-purified VZV glycoproteins (gpELISA).

RESULTS: Robust VZV CMI at HZ onset correlated with reduced HZ morbidity, whereas VZV gpELISA titers did not. Three weeks after HZ onset, gpELISA titers were highest in those with more severe HZ and were slightly increased in placebo recipients (compared with zoster vaccine recipients) and in older individuals. VZV CMI responses to HZ were similar in zoster vaccine and placebo recipients and were not affected by demographic characteristics or antiviral therapy, except for responder cell frequency at HZ onset, which decreased with age. When responses to zoster vaccine and HZ could be compared, VZV CMI values were similar, but antibody titers were lower.

CONCLUSIONS: Higher VZV CMI at HZ onset was associated with reduced HZ severity and less postherpetic neuralgia. Higher antibody titers were associated with increased HZ severity and occurrence of postherpetic neuralgia. HZ and zoster vaccine generated comparable VZV CMI.

DOI10.1086/605611
Alternate JournalJ. Infect. Dis.
PubMed ID19712037
PubMed Central IDPMC4014851
Grant List1R21AI073121-01A2 / AI / NIAID NIH HHS / United States
H12HA00070 / / PHS HHS / United States
M01-RR00865 / RR / NCRR NIH HHS / United States
N01-AI-40029 / AI / NIAID NIH HHS / United States
N01-HD-3-3345 / HD / NICHD NIH HHS / United States
N01-HD-33162 / HD / NICHD NIH HHS / United States
P60 AG 10415 / AG / NIA NIH HHS / United States
R01 AG026006-01 / AG / NIA NIH HHS / United States
R01 AG026364 / AG / NIA NIH HHS / United States
R01 AR049840 / AR / NIAMS NIH HHS / United States
R01 CA 10014152 / CA / NCI NIH HHS / United States
R01 HL079955 / HL / NHLBI NIH HHS / United States
R01 MH 55253 / MH / NIMH NIH HHS / United States
R01 NR009228 / NR / NINR NIH HHS / United States
T32MH19925 / MH / NIMH NIH HHS / United States
U01 AI068632 / AI / NIAID NIH HHS / United States
U01 KD61055-03 / / PHS HHS / United States