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Leflunomide controls rejection in hamster to rat cardiac xenografts.

Publication ,  Journal Article
Xiao, F; Chong, AS; Foster, P; Sankary, H; McChesney, L; Koukoulis, G; Yang, J; Frieders, D; Williams, JW
Published in: Transplantation
October 15, 1994

Leflunomide is an isoxazole derivative that has the ability to prevent acute rejection of cardiac, renal, and skin transplants in strongly rejecting rat models. Furthermore, leflunomide is able to interact synergistically with CsA to inhibit allograft rejection and also reverse ongoing allograft rejection. In vitro studies suggest that the mechanism of action of leflunomide is via an interruption of cytokine signaling in T cells. This study defines the ability of leflunomide to prevent and reverse rejection of concordant xenografts. One hundred nine adult Lewis rats in 13 groups received abdominal heterotopic cardiac transplants from Golden Syrian hamsters. The xenograft survived 3.9 +/-0.3 days without treatment. When leflunomide was given at 2.5, 5, 10, 15, or 20 mg/kg by gavage daily, the cardiac xenograft survivals were 5.0 +/- 0.6, 8.0 +/- 3.0, 52.0 +/- 20.2, 76.5 +/- 21.14, and 58.9 +/- 28.1 days, respectively. The survival rates were 4.0 +/- 0 and 27.7 +/- 28.7 days when CsA was given at 10 and 20 mg/kg i.m., respectively. The combination of CsA at 10 mg/kg with leflunomide at 10 mg/kg or 5 mg/kg prolonged cardiac xenograft survival to 106.0 +/- 50.2 days and > 90 days, respectively. There were no observable side effects in the latter combination. Histologic studies of untreated graft hearts 4 days after transplantation revealed infarction of myocardium and severe RBC extravasation. In contrast, the rejected hamster hearts from long-term survivors showed massive mononuclear cell infiltration and myocardium fibrosis in contrast to the early rejected picture. Therapy with leflunomide begun on day 2 reversed these rejection responses by day 6. In addition, the increase in allospecific IgM titers observed on day 2 was reversed, and the allospecific IgM to IgG isotype switch that occurred in untreated animals was prevented by leflunomide. These observations demonstrate that leflunomide, at nontoxic doses, effectively controlled acute rejection of concordant xenografts and synergistic immunosuppressive effect was achieved with leflunomide and CsA.

Duke Scholars

Published In

Transplantation

ISSN

0041-1337

Publication Date

October 15, 1994

Volume

58

Issue

7

Start / End Page

828 / 834

Location

United States

Related Subject Headings

  • Transplantation, Heterologous
  • Surgery
  • Rats, Inbred Lew
  • Rats
  • Mesocricetus
  • Male
  • Leflunomide
  • Isoxazoles
  • Immunosuppressive Agents
  • Heart Transplantation
 

Citation

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Xiao, F., Chong, A. S., Foster, P., Sankary, H., McChesney, L., Koukoulis, G., … Williams, J. W. (1994). Leflunomide controls rejection in hamster to rat cardiac xenografts. Transplantation, 58(7), 828–834.
Xiao, F., A. S. Chong, P. Foster, H. Sankary, L. McChesney, G. Koukoulis, J. Yang, D. Frieders, and J. W. Williams. “Leflunomide controls rejection in hamster to rat cardiac xenografts.Transplantation 58, no. 7 (October 15, 1994): 828–34.
Xiao F, Chong AS, Foster P, Sankary H, McChesney L, Koukoulis G, et al. Leflunomide controls rejection in hamster to rat cardiac xenografts. Transplantation. 1994 Oct 15;58(7):828–34.
Xiao, F., et al. “Leflunomide controls rejection in hamster to rat cardiac xenografts.Transplantation, vol. 58, no. 7, Oct. 1994, pp. 828–34.
Xiao F, Chong AS, Foster P, Sankary H, McChesney L, Koukoulis G, Yang J, Frieders D, Williams JW. Leflunomide controls rejection in hamster to rat cardiac xenografts. Transplantation. 1994 Oct 15;58(7):828–834.

Published In

Transplantation

ISSN

0041-1337

Publication Date

October 15, 1994

Volume

58

Issue

7

Start / End Page

828 / 834

Location

United States

Related Subject Headings

  • Transplantation, Heterologous
  • Surgery
  • Rats, Inbred Lew
  • Rats
  • Mesocricetus
  • Male
  • Leflunomide
  • Isoxazoles
  • Immunosuppressive Agents
  • Heart Transplantation