Treatment with humanized monoclonal antibody against CD154 prevents acute renal allograft rejection in nonhuman primates
- PMID: 10371508
- DOI: 10.1038/9536
Treatment with humanized monoclonal antibody against CD154 prevents acute renal allograft rejection in nonhuman primates
Abstract
CD154 is the ligand for the receptor CD40. This ligand-receptor pair mediates endothelial and antigen-presenting cell activation, and facilitates the interaction of these cells with T cells and platelets. We demonstrate here that administration of a CD154-specific monoclonal antibody (hu5C8) allows for renal allotransplantation in outbred, MHC-mismatched rhesus monkeys without acute rejection. The effect persisted for more than 10 months after therapy termination, and no additional drug was required to achieve extended graft survival. Indeed, the use of tacrolimus or chronic steroids seemed to antagonize the anti-rejection effect. Monkeys treated with antibody against CD154 remained healthy during and after therapy. The mechanism of action does not require global depletion of T or B cells. Long-term survivors lost their mixed lymphocyte reactivity in a donor-specific manner, but still formed donor-specific antibody and generated T cells that infiltrated the grafted organ without any obvious effect on graft function. Thus, therapy with antibody against CD154 is a promising agent for clinical use in human allotransplantation.
Comment in
-
Graft tolerance: a duel of two signals.Nat Med. 1999 Jun;5(6):616-7. doi: 10.1038/9458. Nat Med. 1999. PMID: 10371494 No abstract available.
Similar articles
-
Treatment with the humanized CD154-specific monoclonal antibody, hu5C8, prevents acute rejection of primary skin allografts in nonhuman primates.Transplantation. 2001 Nov 15;72(9):1473-8. doi: 10.1097/00007890-200111150-00001. Transplantation. 2001. PMID: 11707732
-
Successful conversion from conventional immunosuppression to anti-CD154 monoclonal antibody costimulatory molecule blockade in rhesus renal allograft recipients.Transplantation. 2001 Aug 27;72(4):587-97. doi: 10.1097/00007890-200108270-00006. Transplantation. 2001. PMID: 11544416
-
Humanized anti-CD154 antibody therapy for the treatment of allograft rejection in nonhuman primates.Transplantation. 2002 Oct 15;74(7):940-3. doi: 10.1097/00007890-200210150-00007. Transplantation. 2002. PMID: 12394834
-
Anti-T-cell antibodies for the treatment of acute rejection after renal transplantation.Expert Opin Biol Ther. 2012 Aug;12(8):1031-42. doi: 10.1517/14712598.2012.689278. Epub 2012 May 15. Expert Opin Biol Ther. 2012. PMID: 22583145 Review.
-
Central role for CD40/CD40 ligand (CD154) interactions in transplant rejection.Pediatr Transplant. 1998 Feb;2(1):6-15. Pediatr Transplant. 1998. PMID: 10084754 Review.
Cited by
-
Mechanisms of regulatory T cell counter-regulation by innate immunity.Transplant Rev (Orlando). 2013 Apr;27(2):61-4. doi: 10.1016/j.trre.2013.02.001. Epub 2013 Mar 7. Transplant Rev (Orlando). 2013. PMID: 23474287 Free PMC article. Review.
-
Renal allograft rejection is prevented by adoptive transfer of anergic T cells in nonhuman primates.J Clin Invest. 2005 Jul;115(7):1896-902. doi: 10.1172/JCI23743. Epub 2005 Jun 9. J Clin Invest. 2005. PMID: 15951837 Free PMC article.
-
The Adaptation Model of Immunity: Signal IV Matters Most in Determining the Functional Outcomes of Immune Responses.J Immunol. 2023 Mar 1;210(5):521-530. doi: 10.4049/jimmunol.2200672. J Immunol. 2023. PMID: 36881868 Free PMC article.
-
CD154 blockade modulates the ratio of Treg to Th1 cells and prolongs the survival of allogeneic corneal grafts in mice.Exp Ther Med. 2014 Apr;7(4):827-834. doi: 10.3892/etm.2014.1527. Epub 2014 Feb 7. Exp Ther Med. 2014. PMID: 24660031 Free PMC article.
-
Prevention of airway allograft tolerance by polyinosinic:polycytidylic acid requires type I interferon responsiveness for mouse airway obliteration.J Heart Lung Transplant. 2013 Sep;32(9):914-24. doi: 10.1016/j.healun.2013.06.017. J Heart Lung Transplant. 2013. PMID: 23953819 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials