Synergistic effects of CTLA-4Ig and sirolimus on orthotopic lung-allograft survival and histology

Transplantation. 2003 Aug 15;76(3):489-95. doi: 10.1097/01.TP.0000072374.48680.E0.

Abstract

Background and aims: The combination of CTLA-4Ig with sirolimus can promote indefinite survival in allograft models for which CTLA-4Ig monotherapy is ineffective. We sought to determine whether a limited course of CTLA-4Ig and sirolimus would alter survival of rat orthotopic single-lung transplantations.

Methods: Left lungs of Brown Norway rats were transplanted into four groups of Lewis recipients (n=6 per group): group 1, no treatment; group 2, mCTLA-4Ig (250 microg/day for 4 days); group 3, sirolimus (3 mg/kg per day for 14 days); group 4, combined therapy with sirolimus and mCTLA-4Ig. Graft survival was determined by daily radiologic examination. Histologic grading of rejection and immunohistochemical staining for T and B lymphocytes were carried out at the time of radiologic graft loss.

Results: Rejection of lung allografts in group 1 occurred at a median of 6.5 days. Neither sirolimus nor mCTLA-4Ig monotherapy resulted in significant prolongation of graft survival (median 9.5 and 8.0 days, respectively). Graft survival in group 4 was significantly prolonged compared with all other groups (median 29.5 days), and a significant reduction in histologic grade of rejection was observed following combination therapy compared with all other groups. Infiltration by CD8+ve T cells at the time of rejection was proportionately greater than CD4+ve T-cell infiltration for groups 1, 2, and 3 but not for the combined-therapy group.

Conclusions: A brief course of combined mCTLA-4Ig and sirolimus prolongs graft survival, reduces severity of rejection, and attenuates CD8+ve T-cell infiltration of fully major histocompatibility complex mismatched lung allografts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD
  • Antigens, Differentiation / pharmacology*
  • CD4-Positive T-Lymphocytes / pathology
  • CD8-Positive T-Lymphocytes / pathology
  • CTLA-4 Antigen
  • Drug Synergism
  • Drug Therapy, Combination
  • Graft Survival / drug effects*
  • Immunohistochemistry
  • Immunosuppressive Agents / pharmacology*
  • Lung Transplantation / immunology*
  • Lung Transplantation / pathology*
  • Male
  • Rats
  • Rats, Inbred BN
  • Rats, Inbred Lew
  • Sirolimus / pharmacology*
  • Transplantation, Homologous

Substances

  • Antigens, CD
  • Antigens, Differentiation
  • CTLA-4 Antigen
  • Ctla4 protein, rat
  • Immunosuppressive Agents
  • Sirolimus