首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Immunosuppressive activity of the Chinese medicinal plant Tripterygium wilfordii. II. Prolongation of hamster-to-rat cardiac xenograft survival by combination therapy with the PG27 extract and cyclosporine.
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Immunosuppressive activity of the Chinese medicinal plant Tripterygium wilfordii. II. Prolongation of hamster-to-rat cardiac xenograft survival by combination therapy with the PG27 extract and cyclosporine.

机译:中草药雷公藤的免疫抑制活性。二。 PG27提取物和环孢素联合治疗可延长仓鼠对大鼠心脏异种移植的存活率。

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摘要

BACKGROUND: PG27 is an immunosuppressive fraction purified from an extract of a Chinese medicinal plant Tripterygium wilfordii, which we investigated alone and in combination with cyclosporine (CsA) in a concordant, hamster-to-rat cardiac xenotransplantation model. METHODS: Golden Syrian hamster hearts were heterotopically transplanted into the abdomen of Lewis rat recipients, which were treated intraperitoneally or orally with PG27, CsA, or both. RESULTS: Combination therapy with 30 mg/kg(day of PG27 and CsA at 10 mg/kg/day successfully suppressed acute hamster-to-rat cardiac xenograft rejection. Treatment with PG27 or CsA alone was ineffective. Among several effective combinations, the best regimen involved PG27 at 30 mg/kg/day and CsA at 5 mg/ kg/day from days 8 to 35 and then CsA at 5 mg/kg/day from days 36 to 100, which produced 100% survival beyond 100 days. CsA suppressed the heterospecific lymphocytotoxic antibody response and inhibited IgG but not IgM xenoantibody production (which led to xenograft rejection), whereas PG27 alone did not prevent antibody production. The PG27/CsA combination blocked the lymphocytotoxic antibody response and IgG and IgM xenoantibody production induced by cardiac xenotransplantation. CONCLUSIONS: PG27 combined with CsA substantially prolonged hamster-to-rat cardiac xenograft survival, as well as completely inhibiting xenoantibody production.
机译:背景:PG27是从中草药雷公藤提取物中提取的一种免疫抑制组分,我们将其与环孢素(CsA)一起在一致的仓鼠-大鼠心脏异种移植模型中进行了研究。方法:将金黄叙利亚仓鼠心脏异位移植到Lewis大鼠接受者的腹部,然后腹膜内或口服PG27,CsA或两者同时治疗。结果:30 mg / kg(日剂量的PG27和CsA的剂量为10 mg / kg /天)的联合治疗成功地抑制了仓鼠对大鼠心脏异种移植的排斥反应,仅PG27或CsA的治疗无效,在几种有效的组合中,最佳该方案涉及从第8天到35天以30 mg / kg /天的PG27和5 mg / kg /天的CsA,然后从第36天到100天以5 mg / kg /天的CsA进行治疗,可在100天后产生100%的存活率。抑制异种淋巴细胞毒性抗体反应并抑制IgG,但不抑制IgM异种抗体的产生(这导致异种移植排斥),而仅PG27不能阻止抗体产生; PG27 / CsA组合可阻断心脏诱导的淋巴细胞毒性抗体反应以及IgG和IgM异种抗体的产生结论:PG27结合CsA大大延长了仓鼠对大鼠心脏异种移植的存活,并完全抑制了异种抗体的产生。

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