Ectopic B7-H4-Ig expression attenuates concanavalin A-induced hepatic injury

Clin Immunol. 2010 Jul;136(1):30-41. doi: 10.1016/j.clim.2010.02.022. Epub 2010 Mar 25.

Abstract

Previous studies demonstrate that both membrane B7-H4 and B7-H4-Ig fusion protein could inhibit T-cell responses. In the present study, we explored the potential effect of B7-H4-Ig on liver injury in a hepatitis mouse model induced by concanavalin A (ConA). A B7-H4-Ig construct was introduced into animals by the hydrodynamic gene delivery approach. It was found that ectopic expression of B7-H4-Ig could inhibit ConA-induced elevation of serum levels of ALT and AST, suppress liver necrosis and even mortality of mice. Furthermore, we observed that pretreatment of B7-H4-Ig dramatically decreased serum levels and the expression of mRNA for IL-2, IFN-gamma and IL-4, but increased IL-10 in ConA-treated mice. Our results suggest that B7-H4-Ig may protect animals from liver injury induced by ConA, which could be associated with reduced serum levels for IL-2, IFN-gamma and IL-4 as well as enhanced IL-10 production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • B7-1 Antigen / blood
  • B7-1 Antigen / genetics
  • B7-1 Antigen / metabolism
  • B7-1 Antigen / therapeutic use*
  • Chemical and Drug Induced Liver Injury / blood
  • Chemical and Drug Induced Liver Injury / pathology
  • Chemical and Drug Induced Liver Injury / prevention & control*
  • Concanavalin A / pharmacology*
  • Gene Expression / drug effects
  • Gene Expression / genetics
  • Gene Transfer Techniques
  • Genetic Therapy / methods*
  • Humans
  • Immunoglobulin Fc Fragments / blood
  • Immunoglobulin Fc Fragments / genetics*
  • Immunoglobulin G / genetics*
  • Interferon-gamma / blood
  • Interferon-gamma / genetics
  • Interleukin-10 / blood
  • Interleukin-10 / genetics
  • Interleukin-2 / blood
  • Interleukin-2 / genetics
  • Interleukin-4 / blood
  • Interleukin-4 / genetics
  • Leukocytes, Mononuclear / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Liver / pathology
  • Mice
  • Mice, Inbred BALB C
  • Necrosis / chemically induced
  • Necrosis / pathology
  • Recombinant Fusion Proteins / blood
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Fusion Proteins / therapeutic use*
  • Survival Analysis
  • V-Set Domain-Containing T-Cell Activation Inhibitor 1

Substances

  • B7-1 Antigen
  • Immunoglobulin Fc Fragments
  • Immunoglobulin G
  • Interleukin-2
  • Recombinant Fusion Proteins
  • V-Set Domain-Containing T-Cell Activation Inhibitor 1
  • Vtcn1 protein, mouse
  • Concanavalin A
  • Interleukin-10
  • Interleukin-4
  • Interferon-gamma
  • Aspartate Aminotransferases
  • Alanine Transaminase