The role of the CD134-CD134 ligand costimulatory pathway in alloimmune responses in vivo

J Immunol. 2003 Mar 15;170(6):2949-55. doi: 10.4049/jimmunol.170.6.2949.

Abstract

The CD134-CD134 ligand (CD134L) costimulatory pathway has been shown to be critical for both T and B cell activation; however, its role in regulating the alloimmune response remains unexplored. Furthermore, its interactions with other costimulatory pathways and immunosuppressive agents are unclear. We investigated the effect of CD134-CD134L pathway blockade on allograft rejection in fully MHC-mismatched rat cardiac and skin transplantation models. CD134L blockade alone did not prolong graft survival compared with that of untreated recipients, and in combination with donor-specific transfusion, cyclosporine, or rapamycin, was less effective than B7 blockade in prolonging allograft survival. However, in combination with B7 blockade, long-term allograft survival was achieved in all recipients (>200 days). Moreover, this was synergistic in reducing the frequency of IFN-gamma-producing alloreactive lymphocytes and inhibiting the generation of activated/effector lymphocytes. Most impressively, this combination prevented rejection in a presensitized model using adoptive transfer of primed lymphocytes into athymic heart transplant recipients. In comparison to untreated recipients (mean survival time (MST): 5.3 +/- 0.5 days), anti-CD134L mAb alone modestly prolonged allograft survival (MST: 14 +/- 2.8 days) as did CTLA4Ig (MST: 21.5 +/- 1.7 days), but all grafts were rejected within 24 days. Importantly, combined blockade further and significantly prolonged allograft survival (MST: 75.3 +/- 12.7 days) and prevented the expansion and/or persistence of primed/effector alloreactive T cells. Our data suggest that CD134-CD134L is a critical pathway in alloimmune responses, especially recall/primed responses, and is synergistic with CD28-B7 in mediating T cell effector responses during allograft rejection. Understanding the mechanisms of collaboration between these different pathways is important for the development of novel strategies to promote long-term allograft survival.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abatacept
  • Animals
  • Antibodies, Monoclonal / administration & dosage
  • B7-1 Antigen / immunology
  • CD28 Antigens / immunology
  • Drug Synergism
  • Graft Rejection / immunology
  • Heart Transplantation / immunology
  • Immunization
  • Immunoconjugates / administration & dosage
  • Immunosuppressive Agents / administration & dosage
  • Injections, Intraperitoneal
  • Interferon-gamma / biosynthesis
  • Isoantigens / immunology*
  • Ligands
  • Lymphocyte Activation / immunology*
  • Lymphocyte Count
  • Lymphocyte Subsets / immunology
  • Lymphocyte Subsets / metabolism
  • Male
  • Membrane Glycoproteins / antagonists & inhibitors
  • Membrane Glycoproteins / metabolism
  • Membrane Glycoproteins / physiology*
  • Rats
  • Rats, Inbred Lew
  • Rats, Inbred WF
  • Rats, Nude
  • Receptors, OX40
  • Receptors, Tumor Necrosis Factor*
  • Skin Transplantation / immunology
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / metabolism
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / physiology*
  • Tumor Necrosis Factors

Substances

  • Antibodies, Monoclonal
  • B7-1 Antigen
  • CD28 Antigens
  • Immunoconjugates
  • Immunosuppressive Agents
  • Isoantigens
  • Ligands
  • Membrane Glycoproteins
  • Receptors, OX40
  • Receptors, Tumor Necrosis Factor
  • Tnfrsf4 protein, rat
  • Tnfsf4 protein, rat
  • Tumor Necrosis Factor Receptor Superfamily, Member 7
  • Tumor Necrosis Factors
  • Abatacept
  • Interferon-gamma