IDEC-131 (anti-CD154), sirolimus and donor-specific transfusion facilitate operational tolerance in non-human primates

Am J Transplant. 2005 May;5(5):1032-41. doi: 10.1111/j.1600-6143.2005.00796.x.

Abstract

CD154-specific antibody therapy prevents allograft rejection in many experimental transplant models. However, initial clinical transplant trials with anti-CD154 have been disappointing suggesting the need for as of yet undetermined adjuvant therapy. In rodents, donor antigen (e.g., a donor blood transfusion), or mTOR inhibition (e.g., sirolimus), enhances anti-CD154's efficacy. We performed renal transplants in major histocompatibility complex-(MHC) mismatched rhesus monkeys and treated recipients with combinations of the CD154-specific antibody IDEC-131, and/or sirolimus, and/or a pre-transplant donor-specific transfusion (DST). Therapy was withdrawn after 3 months. Triple therapy prevented rejection during therapy in all animals and led to operational tolerance in three of five animals including donor-specific skin graft acceptance in the two animals tested. IDEC-131, sirolimus and DST are highly effective in preventing renal allograft rejection in primates. This apparently clinically applicable regimen is promising for human renal transplant trials.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology*
  • Antibodies, Monoclonal, Humanized
  • Blood Transfusion
  • CD3 Complex / biosynthesis
  • CD40 Ligand / immunology*
  • Graft Rejection
  • Graft Survival / drug effects
  • Immunosuppressive Agents / pharmacology*
  • Isoantibodies / chemistry
  • Kidney Transplantation / methods
  • Leukocytes, Mononuclear / metabolism
  • Lymphocyte Culture Test, Mixed
  • Lymphocytes / metabolism
  • Macaca mulatta
  • Major Histocompatibility Complex
  • Primates
  • Protein Kinases / metabolism
  • Sirolimus / pharmacology*
  • Skin Transplantation
  • TOR Serine-Threonine Kinases
  • Time Factors

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • CD3 Complex
  • Immunosuppressive Agents
  • Isoantibodies
  • CD40 Ligand
  • Protein Kinases
  • MTOR protein, human
  • TOR Serine-Threonine Kinases
  • toralizumab
  • Sirolimus