Moderate alcohol consumption enhances vaccine-induced responses in rhesus macaques

  • I. Messaoudi
  • , M. Asquith
  • , F. Engelmann
  • , B. Park
  • , M. Brown
  • , A. Rau
  • , J. Shaw
  • , K. A. Grant

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

We have recently shown that chronic alcohol consumption in a rhesus macaque model of ethanol self-administration significantly modulates the serum cytokine profile. In this study, we extended these observations by investigating the impact of chronic ethanol exposure on the immune response to Modified Vaccinia Ankara (MVA). All animals were vaccinated with MVA before ethanol exposure to ethanol and then again after 7 months of 22. h/day of "open-access" drinking of 4% (w/v) ethanol. Our results indicate that animals whose blood ethanol concentration (BEC) chronically exceeded 80. mg/dl had lower CD4 and CD8 T cell proliferation as well as IgG responses following MVA booster than control animals. In contrast, relatively moderate drinkers whose BEC remained below 80. mg/ml exhibited more robust MVA-specific IgG and CD8 T cell responses than controls. To begin to uncover mechanisms underlying the differences in MVA-specific responses between the three groups, we analyzed plasma cytokine levels and microRNA expression in peripheral blood mononuclear cells following MVA booster. Our findings suggest that moderate ethanol consumption results in higher levels of antiviral cytokines and an expression profile of microRNAs linked to CD8 T cell differentiation. In summary, moderate alcohol consumption enhances recall vaccine responses, whereas chronic alcohol intoxication suppresses this response.

Original languageEnglish
Pages (from-to)54-61
Number of pages8
JournalVaccine
Volume32
Issue number1
DOIs
StatePublished - Dec 17 2013

Funding

The authors would like to thank Dr. Kevin Nusser for his expert support and help in the completion of the animal studies. This work was funded by NIH 8P51 ODO11092-53 and NIH/NIAAA R24 AA019431 , U01 AA13641 , U01 AA1351 0 and NIH/NIAAA R21AA021947 .

Funder number
8P51 ODO11092-53
R24 AA019431, U01 AA1351 0, U01 AA13641
R21AA021947

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Antibody
    • Cytokine
    • Ethanol
    • MVA
    • Macaque
    • MicroRNA
    • T cell
    • Vaccine

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