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Prophylactic immunosuppression with anti-interleukin-2 receptor monoclonal antibody LO-Tact-1 versus OKT3 in liver allografting. A two-year follow-up study.

作者信息

Reding R, Feyaerts A, Vraux H, Latinne D, De La Parra B, Cornet A, Cormont F, Jamart J, Sokal E, de Ville de Goyet J, Lerut J, Bazin H, Otte J B

机构信息

Department of Surgery, University of Louvain Medical School, Brussels, Belgium.

出版信息

Transplantation. 1996 May 15;61(9):1406-9. doi: 10.1097/00007890-199605150-00022.

DOI:10.1097/00007890-199605150-00022
PMID:8629306
Abstract

A prospective trial was conducted in 129 recipients of primary liver transplantation, to compare induction immunosuppression using triple drug therapy (cyclosporine, steroids, and azathioprine; group 1, n = 42), versus triple drug therapy with a 10-day course of OKT3 (group 2, n = 44) or of the anti-interleukin-2 receptor monoclonal antibody LO-Tact-1 (group 3, n = 43). Two-year actual patient survival rates were 64%, 79%, and 93% in groups 1, 2, and 3, respectively (1 vs. 2, NS; I vs. III, P = 0.003; 2 vs. 3, NS). Up to 2 years after transplantation, 18%, 44%, and 53% of the grafts in groups 1, 2, and 3, respectively, had not experienced steroid-resistant acute rejection (1 vs. 2, P = 0.002; 1 vs. 3, P = 0.007; 2 vs. 3, NS). The overall incidence of chronic rejection was 4%. OKT3 therapy, but not LO-Tact-1, significantly increased the incidence of cytomegalovirus infections (P = 0.019). In conclusion, immunoprophylaxis with LO-Tact-1 seemed to provide a liver graft acceptance rate at least as satisfactory as that with OKT3, without an increase in the incidence of infections.

摘要

相似文献

1
Prophylactic immunosuppression with anti-interleukin-2 receptor monoclonal antibody LO-Tact-1 versus OKT3 in liver allografting. A two-year follow-up study.
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2
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2
Antibody induction versus placebo, no induction, or another type of antibody induction for liver transplant recipients.肝移植受者的抗体诱导与安慰剂、无诱导或另一种抗体诱导方式的比较。
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Antibody induction versus corticosteroid induction for liver transplant recipients.
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Cochrane Database Syst Rev. 2014 May 31;2014(5):CD010252. doi: 10.1002/14651858.CD010252.pub2.
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