Influence of age and nature of primary infection on varicella-zoster virus-specific cell-mediated immune responses

J Infect Dis. 2010 Apr 1;201(7):1024-30. doi: 10.1086/651199.

Abstract

Background: Varicella-zoster virus (VZV)-specific cell-mediated immunity is important for protection against VZV disease. We studied the relationship between VZV cell-mediated immunity and age after varicella or VZV vaccination in healthy and human immunodeficiency virus (HIV)-infected individuals.

Methods: VZV responder cell frequency (RCF) determinations from 752 healthy and 200 HIV-infected subjects were used to identify group-specific regression curves on age.

Results: In healthy individuals with past varicella, VZV RCF peaked at 34 years of age. Similarly, VZV-RCF after varicella vaccine increased with age in subjects aged <1 to 43 years. In subjects aged 61-90 years, VZV RCF after zoster vaccine decreased with age. HIV-infected children had lower VZV RCF estimates than HIV-infected adults. In both groups, VZV RCF results were low and constant over age. Varicella vaccination of HIV-infected children with CD4 levels 20% generated VZV RCF values higher than wild-type infection and comparable to vaccine-induced responses of healthy children.

Conclusions: In immunocompetent individuals with prior varicella, VZV RCF peaked in early adulthood. Administration of varicella vaccine to HIV-infected or uninfected individuals aged >5 years generated VZV RCF values similar to those of immunocompetent individuals with immunity induced by wild-type infection. A zoster vaccine increased the VZV RCF of elderly adults aged <75 years to values higher than peak values induced by wild-type infection.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Aged
  • Aged, 80 and over
  • CD4-Positive T-Lymphocytes / immunology
  • Chickenpox / immunology*
  • Chickenpox Vaccine / immunology*
  • Child
  • Child, Preschool
  • HIV Infections / immunology
  • Herpesvirus 3, Human / immunology*
  • Humans
  • Immunity, Cellular / immunology
  • Infant
  • Logistic Models
  • Longitudinal Studies
  • Middle Aged

Substances

  • Chickenpox Vaccine