C1-inhibitor attenuates hyperacute rejection and inhibits complement, leukocyte and platelet activation in an ex vivo pig-to-human perfusion model

Immunopharmacology. 1999 May;42(1-3):231-43. doi: 10.1016/s0162-3109(99)00008-9.

Abstract

Xenotransplantation may be a future alternative due to increased shortage of organs. Classical complement activation is central in hyperacute rejection in pig-to-human combinations. We investigated the effects of C1-inhibitor (C1-INH), a regulator of the complement and contact systems, on hyperacute rejection. Pig kidneys were perfused with fresh human blood to which either C1-INH (n = 6) or human serum albumin (n = 6) was added. The survival of the C1-INH perfused kidneys (mean 327 min) was significantly longer (p < 0.00001) than the controls (79 min). C1-INH substantially inhibited complement activation (C1rs-C1-INH complexes, C4bc, C3bc and terminal complement complex) (p < 0.001 for all) compared with the marked complement activation in the controls. No contact activation was found. Leukocytes and platelets were substantially activated (counts, myeloperoxidase, beta-thromboglobulin, thrombospondin, soluble P-selectin) in the control group, and this activation was markedly reduced by C1-INH (p < 0.02 for all). Immunohistochemistry showed less C1q, C3, TCC, IgG and fibrin deposition in the C1-INH group. C1-INH may be useful to attenuate hyperacute rejection, probably through inhibition of complement. The reduced activation of neutrophils and platelets may mainly be secondary to inhibition of complement.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens / immunology
  • Complement C1 / immunology
  • Complement C1 Inactivator Proteins / immunology
  • Complement C1 Inactivator Proteins / therapeutic use*
  • Complement C3b / metabolism
  • Complement Pathway, Classical / immunology*
  • Female
  • Graft Rejection / immunology
  • Graft Rejection / prevention & control*
  • Graft Survival / drug effects
  • Graft Survival / immunology
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Kidney / blood supply
  • Kidney / cytology
  • Kidney / immunology
  • Kidney / metabolism
  • Kidney Transplantation / immunology*
  • Kininogens / metabolism
  • Leukocytes / immunology*
  • Lymphocyte Activation / immunology
  • Male
  • Neutrophil Activation / immunology
  • Perfusion
  • Platelet Activation / immunology*
  • Prekallikrein / metabolism
  • Swine
  • Transplantation, Heterologous / immunology*

Substances

  • Antigens
  • Complement C1
  • Complement C1 Inactivator Proteins
  • Kininogens
  • Complement C3b
  • Prekallikrein