CD8+ T cells prevent antigen-induced antibody-dependent enhancement of dengue disease in mice

J Immunol. 2014 Oct 15;193(8):4117-24. doi: 10.4049/jimmunol.1401597. Epub 2014 Sep 12.

Abstract

Dengue virus (DENV) causes pathologies ranging from the febrile illness dengue fever to the potentially lethal severe dengue disease. A major risk factor for developing severe dengue disease is the presence of subprotective DENV-reactive Abs from a previous infection (or from an immune mother), which can induce Ab-dependent enhancement of infection (ADE). However, infection in the presence of subprotective anti-DENV Abs does not always result in severe disease, suggesting that other factors influence disease severity. In this study we investigated how CD8(+) T cell responses influence the outcome of Ab-mediated severe dengue disease. Mice were primed with aluminum hydroxide-adjuvanted UV-inactivated DENV prior to challenge with DENV. Priming failed to induce robust CD8(+) T cell responses, and it induced nonneutralizing Ab responses that increased disease severity upon infection. Transfer of exogenous DENV-activated CD8(+) T cells into primed mice prior to infection prevented Ab-dependent enhancement and dramatically reduced viral load. Our results suggest that in the presence of subprotective anti-DENV Abs, efficient CD8(+) T cell responses reduce the risk of Ab-mediated severe dengue disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic
  • Adoptive Transfer
  • Animals
  • Antibodies, Viral / immunology*
  • Antibody-Dependent Enhancement / immunology*
  • Antigens, Viral / immunology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / transplantation*
  • Dengue / immunology
  • Dengue / prevention & control*
  • Dengue Virus / immunology*
  • Immunization, Passive
  • Immunoglobulin G / immunology
  • Mice
  • Mice, Transgenic
  • Viral Load / immunology

Substances

  • Adjuvants, Immunologic
  • Antibodies, Viral
  • Antigens, Viral
  • Immunoglobulin G