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Relationship between cell-mediated immunity to Varicella-Zoster virus and aging in subjects from the community-based Shozu Herpes Zoster study.
Shirane, Risako; Tang, Huamin; Hayashi, Kenichi; Okuno, Yoshinobu; Iso, Hiroyasu; Asada, Hideo; Yamanishi, Koichi; Mori, Yasuko.
Afiliação
  • Shirane R; Division of Clinical Virology, Center for Infectious Diseases, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Tang H; Division of Clinical Virology, Center for Infectious Diseases, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Hayashi K; Department of Immunology, Nanjing Medical University, Nanjing, China.
  • Okuno Y; Department of Mathematics, Keio University, Yokohama, Japan.
  • Iso H; The Research Foundation for Microbial Diseases of Osaka University, Kagawa, Japan.
  • Asada H; Public Health, Department of Social Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Yamanishi K; Department of Dermatology, Nara Medical University School of Medicine, Nara, Japan.
  • Mori Y; The Research Foundation for Microbial Diseases of Osaka University, Kagawa, Japan.
J Med Virol ; 89(2): 313-317, 2017 02.
Article em En | MEDLINE | ID: mdl-27420414
ABSTRACT
Age-related declines in cell-mediated immunity (CMI) are associated with the incidence and severity of Herpes Zoster (HZ) infection. However, the level of Varicella-Zoster virus (VZV)-specific CMI associated with disease onset is unclear. This study aimed to examine factors associated with VZV-specific CMI, as measured by an interferon-gamma (IFN-γ) enzyme-linked immunospot (ELISPOT) assay, in a Japanese cohort. The study enrolled 365 subjects aged 60 years and over, all of whom were taking part in the Shozu Herpes Zoster (SHEZ) study and had undergone four sets of blood and intradermal reaction tests during a 3 year follow-up period. The VZV-specific immunity profile of each subject was assessed, and linear mixed effects models were constructed to analyze IFN-γ ELISPOT results in association with a combination of factors. The model that best explained the IFN-γ ELISPOT results was selected using the Akaike Information Criteria. The best-fit model consisted of age group as the only explanatory fixed-effect variable. The model showed that VZV-specific CMI, quantified as numbers of spots on the ELISPOT assay, among subjects aged 70-79 was on average 10.30 points lower than that among subjects aged 60-69. There was no statistically significant difference between subjects aged 70-79 and those aged 80-89. Age was the only factor significantly associated with the level of VZV-specific CMI, as measured by the IFN-γ ELISPOT assay. These results may represent an important step towards quantifying the relationship between VZV-specific CMI and the onset of HZ. J. Med. Virol. 89313-317, 2017. © 2016 Wiley Periodicals, Inc.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Envelhecimento / Herpesvirus Humano 3 / Imunidade Celular Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: J Med Virol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Envelhecimento / Herpesvirus Humano 3 / Imunidade Celular Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: J Med Virol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão