Effect of influenza virus vaccine on the expression of human immunodeficiency virus co-receptor CCR5

Ann Allergy Asthma Immunol. 2004 Sep;93(3):272-6. doi: 10.1016/S1081-1206(10)61500-1.

Abstract

Background: Administration of influenza vaccine to human immunodeficiency virus (HIV)-infected children can lead to increased viral load. CCR5 and CXCR4 are known to play an important role in HIV cell entry and viral replication.

Objective: To determine the effects of influenza vaccine on chemokine receptors and on viral load in HIV-infected children.

Methods: Eight HIV-infected children receiving stable therapy and 11 healthy adults were enrolled. Chemokine expression and immune activation were determined before and 48 hours after influenza vaccination. CCR5 and beta-chemokine gene expression were analyzed using real-time polymerase chain reaction. Viral load was measured at baseline, 48 hours, and 6 to 12 weeks.

Results: Forty-eight hours after influenza vaccination, mean CCR5 expression was significantly decreased on the CD3 (21.1% vs 11.3% in HIV-infected children; P = .02; and 18.3% vs 10.7% in controls; P = .008) and CD4 (13.0% vs 3.6% in the HIV group; P = .04; and 13.6% vs 6.5% in controls; P = .02) lymphocytes. This was observed in conjunction with an increase in HLA-DR expression on T lymphocytes in HIV-infected children (P = .046). No significant changes were observed in HIV viral load, CD3 and CD8 lymphocyte counts, expression of interleukin 2 receptor and CXCR4, or gene expression of CCR5 and beta-chemokines 48 hours after vaccination.

Conclusions: Influenza virus vaccine markedly decreased chemokine receptor CCR5 expression on CD4 T lymphocytes. However, this immunomodulatory effect does not seem to affect overall viral replication in HIV-infected children who received highly active antiretroviral therapy.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antiretroviral Therapy, Highly Active
  • CD4-Positive T-Lymphocytes / drug effects*
  • CD4-Positive T-Lymphocytes / metabolism
  • Child
  • Child, Preschool
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Depression, Chemical
  • Female
  • Gene Expression Regulation / drug effects
  • Genes, MHC Class II / drug effects
  • HIV Infections / drug therapy
  • HIV Infections / immunology
  • HIV Infections / metabolism*
  • HIV Infections / virology
  • HIV-1 / drug effects
  • HIV-1 / physiology
  • HLA-DR Antigens / biosynthesis
  • Humans
  • Influenza Vaccines / pharmacology*
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / genetics
  • Lymphocyte Count
  • Lymphocyte Subsets
  • Male
  • Receptors, CCR5 / biosynthesis*
  • Receptors, CCR5 / genetics
  • Viral Load
  • Virus Replication / drug effects

Substances

  • Cytokines
  • HLA-DR Antigens
  • Influenza Vaccines
  • Receptors, CCR5
  • Interferon-gamma