The suppression of inflammatory macrophage-mediated cytotoxicity and proinflammatory cytokine production by transgenic expression of HLA-E

Transpl Immunol. 2013 Dec;29(1-4):76-81. doi: 10.1016/j.trim.2013.08.001. Epub 2013 Aug 29.

Abstract

Background: Macrophages participate in xenogenic rejection and represent a major biological obstacle to successful xenotransplantation. The signal inhibitory regulatory protein α (SIRPα) receptor was reported to be a negative regulator of macrophage phagocytic activity via interaction with CD47, its ligand. Because a majority of human macrophages express the inhibitory receptor CD94/NKG2A, which binds specifically to the human leukocyte antigen (HLA)-E and contains immunoreceptor tyrosine-based inhibition motifs (ITIMs), the inhibitory function of HLA class I molecules, HLA-E, on macrophage-mediated cytolysis was examined. The suppressive effect against proinflammatory cytokine production by macrophages was also examined.

Methods: Complementary DNA (cDNA) of HLA-E, and CD47 were prepared and transfected into swine endothelial cells (SEC). The expression of the modified genes was evaluated by flow cytometry and macrophage-mediated cytolysis was assessed using in vitro generated macrophages.

Results: Transgenic expression of HLA-E significantly suppressed the macrophage-mediated cytotoxicity. HLA-E transgenic expression demonstrated a significant suppression equivalent to CD47 transgenic expression. Furthermore, transgenic HLA-E suppressed the production of pro-inflammatory cytokines by inflammatory macrophages.

Conclusions: These results indicate that generating transgenic HLA-E pigs might protect porcine grafts from, not only NK cytotoxicity, but also macrophage-mediated cytotoxicity.

Keywords: HLA-E; Immunoreceptor tyrosine-based inhibition motif (ITIM); Inflammatory macrophage; Pro-inflammatory cytokine; Xenocytotoxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD47 Antigen / genetics
  • CD47 Antigen / immunology
  • CD47 Antigen / metabolism
  • Cell Line
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Cytokines / immunology*
  • Endothelial Cells / immunology*
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Gene Expression
  • HLA-E Antigens
  • Heterografts
  • Histocompatibility Antigens Class I / biosynthesis
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / immunology*
  • Humans
  • Inflammation
  • Inflammation Mediators / immunology*
  • Inflammation Mediators / metabolism
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Macrophages / pathology
  • Organ Transplantation*
  • Swine
  • Transgenes*
  • Transplantation Tolerance*

Substances

  • CD47 Antigen
  • CD47 protein, human
  • Cytokines
  • Histocompatibility Antigens Class I
  • Inflammation Mediators