Immunosuppressive activity of the Chinese medicinal plant Tripterygium wilfordii - I. Prolongation of rat cardiac and renal allograft survival by thePG27 extract and immunosuppressive synergy in combination therapy with cyclosporine

Citation
J. Wang et al., Immunosuppressive activity of the Chinese medicinal plant Tripterygium wilfordii - I. Prolongation of rat cardiac and renal allograft survival by thePG27 extract and immunosuppressive synergy in combination therapy with cyclosporine, TRANSPLANT, 70(3), 2000, pp. 447-455
Citations number
36
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
TRANSPLANTATION
ISSN journal
00411337 → ACNP
Volume
70
Issue
3
Year of publication
2000
Pages
447 - 455
Database
ISI
SICI code
0041-1337(20000815)70:3<447:IAOTCM>2.0.ZU;2-6
Abstract
Background. PG27 is an immunosuppressive fraction purified from an extract of a Chinese medicinal plant, Tripterygium wilfordii. We tested PG27 in rat cardiac and renal allotransplantation, and we examined the immunosuppressi ve interaction with cyclosporine (CsA). Methods. Brown Norway (BN) rat heart or kidney allografts were transplanted into the abdomen of Lewis rats, which were treated by the intraperitoneal or oral route with PG27, CsA, or both. Results, PG27 administered intraperitoneally to Lewis recipients for 16 day s at 10-30 mg/kg/day significantly increased the median survival time of BN heart allografts from 7 to 18-22 days. Oral administration was effective, with cardiac allograft survival prolonged to >100 days with 52 days of trea tment. PG27 at 20-30 mg/kg/day significantly extended the median survival t ime of BN kidney allograft recipients from 9 to 36.5-77 days, and 30 mg/kg/ day for 52 days extended survival beyond 200 days. PG27 combined with CsA s ignificantly enhanced heart and kidney allograft survival, even at doses of CsA ineffective when administered alone, The addition of 5 or 10 mg/kg/day PG27 reduced by 50-75% the CsA dose needed for 100% kidney allograft survi val. The combination index was less than 1.0, indicating synergy of PG27 wi th CsA in prolonging cardiac and renal allograft survival. Furthermore, the PG27/CsA combination exerted a positive influence on renal allograft funct ion. PG490 (triptolide, a constituent of PG27) and PG490-88 (a semisyntheti c derivative of PG490) suppressed rejection of cardiac and renal allografts . Conclusions. The PG27 herbal extract demonstrated immunosuppressive activit y by prolonging heart and kidney allograft survival, displaying synergy in the immunosuppressive interaction with CsA, and improving renal allograft f unction in combination with CsA. PG490 and PG490-88 compounds were also eff ective.