CD49a promotes T-cell-mediated hepatitis by driving T helper 1 cytokine and interleukin-17 production

Immunology. 2014 Mar;141(3):388-400. doi: 10.1111/imm.12201.

Abstract

It is becoming increasingly clear that the T-cell-mediated immune response is important in many diseases. In this study, we used concanavalin A (Con A) -induced hepatitis to investigate the role of CD49a in the molecular and cellular mechanism of the T-cell-mediated immune response. We found that CD49a(-/-) mice had significantly reduced levels of serum alanine aminotransferase and were protected from Con A-induced hepatitis. CD49a deficiency led to decreased production of interferon-γ (IFN-γ) and interleukin-17A (IL-17A) after Con A injection. Furthermore, we found that hepatic CD4(+) T cells and invariant natural killer T cells up-regulated CD49a expression, along with enhanced activation after Con A injection, leading to production of inflammatory cytokines by these T cells. Blockade of CD49a in vivo ameliorated Con A-induced hepatitis with reduced production of IFN-γ and IL-17A. Hence, CD49a promoted Con A-induced hepatitis through enhancing inflammatory cytokine production (IFN-γ and IL-17A) by CD4(+) T and invariant natural killer T cells. The protective effect of CD49a blockade antibody suggested a new target therapeutic molecule for intervention of T-cell-mediated liver injury.

Keywords: CD49a; T-cell-mediated hepatitis; interferon-γ; interleukin-17A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Biomarkers / blood
  • Cells, Cultured
  • Chemical and Drug Induced Liver Injury / etiology
  • Chemical and Drug Induced Liver Injury / genetics
  • Chemical and Drug Induced Liver Injury / immunology
  • Chemical and Drug Induced Liver Injury / metabolism*
  • Chemical and Drug Induced Liver Injury / prevention & control
  • Concanavalin A
  • Disease Models, Animal
  • Immunity, Cellular*
  • Inflammation Mediators / blood
  • Inflammation Mediators / metabolism*
  • Integrin alpha1 / genetics
  • Integrin alpha1 / metabolism*
  • Interferon-gamma / metabolism
  • Interleukin-17 / blood
  • Interleukin-17 / metabolism*
  • Lymphocyte Activation
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Natural Killer T-Cells / immunology
  • Natural Killer T-Cells / metabolism
  • Th1 Cells / immunology
  • Th1 Cells / metabolism*
  • Time Factors

Substances

  • Biomarkers
  • Il17a protein, mouse
  • Inflammation Mediators
  • Integrin alpha1
  • Interleukin-17
  • Concanavalin A
  • Interferon-gamma
  • Alanine Transaminase