Recombinant human C1-inhibitor prevents acute antibody-mediated rejection in alloimmunized baboons
- PMID: 20336054
- DOI: 10.1038/ki.2010.75
Recombinant human C1-inhibitor prevents acute antibody-mediated rejection in alloimmunized baboons
Abstract
Acute antibody-mediated rejection is an unsolved issue in transplantation, especially in the context of pretransplant immunization. The deleterious effect of preformed cytotoxic anti-HLA antibodies through complement activation is well proven, but very little is known concerning complement blockade to prevent/cure this rejection. Here, we used a baboon model of preimmunization to explore the prevention of acute antibody-mediated rejection by an early inhibition of the classical complement pathway using human recombinant C1-inhibitor. Baboons were immunized against peripheral blood mononuclear cells from allogeneic donors and, once a specific and stable immunization had been established, they received a kidney from the same donor. Rejection occurred at day 2 posttransplant in untreated presensitized recipients, with characteristic histological lesions and complement deposition. As recombinant human C1-inhibitor blocks in vitro cytotoxicity induced by donor-specific antibodies, other alloimmunized baboons received the drug thrice daily intravenously during the first 5 days after transplant. Rejection was prevented during this treatment but occurred after discontinuation of treatment. We show here that early blockade of complement activation by recombinant human C1-inhibitor can prevent acute antibody-mediated rejection in presensitized recipients. This treatment could also be useful in other forms of acute antibody-mediated rejection caused by induced antibodies.
Comment in
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A complementary approach to treating antibody-mediated transplant rejection.Kidney Int. 2010 Jul;78(2):125-7. doi: 10.1038/ki.2010.80. Kidney Int. 2010. PMID: 20588285
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