[HTML][HTML] Recombinant human C1-inhibitor prevents acute antibody-mediated rejection in alloimmunized baboons

X Tillou, N Poirier, S Le Bas-Bernardet, J Hervouet… - Kidney international, 2010 - Elsevier
X Tillou, N Poirier, S Le Bas-Bernardet, J Hervouet, D Minault, K Renaudin, F Vistoli
Kidney international, 2010Elsevier
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 …
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.
Elsevier