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来氟米特可控制仓鼠对大鼠心脏异种移植的排斥反应。

Leflunomide controls rejection in hamster to rat cardiac xenografts.

作者信息

Xiao F, Chong A S, Foster P, Sankary H, McChesney L, Koukoulis G, Yang J, Frieders D, Williams J W

机构信息

Department of General Surgery, Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612.

出版信息

Transplantation. 1994 Oct 15;58(7):828-34.

PMID:7940718
Abstract

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.

摘要

来氟米特是一种异恶唑衍生物,在强烈排斥的大鼠模型中,它有能力预防心脏、肾脏和皮肤移植的急性排斥反应。此外,来氟米特能够与环孢素协同作用,抑制同种异体移植排斥反应,还能逆转正在进行的同种异体移植排斥反应。体外研究表明,来氟米特的作用机制是通过中断T细胞中的细胞因子信号传导。本研究确定了来氟米特预防和逆转协调性异种移植排斥反应的能力。13组共109只成年Lewis大鼠接受了来自金黄叙利亚仓鼠的腹部异位心脏移植。未经治疗的情况下,异种移植心脏存活3.9±0.3天。当每天通过灌胃给予来氟米特2.5、5、10、15或20mg/kg时,心脏异种移植的存活时间分别为5.0±0.6、8.0±3.0、52.0±20.2、76.5±21.14和58.9±28.1天。当分别肌肉注射10mg/kg和20mg/kg环孢素时,存活时间分别为4.0±0天和27.7±28.7天。10mg/kg环孢素与10mg/kg或5mg/kg来氟米特联合使用时,心脏异种移植的存活时间分别延长至106.0±50.2天和>90天。后一种联合使用没有观察到明显的副作用。移植后4天对未经治疗的移植心脏进行组织学研究,发现心肌梗死和严重的红细胞外渗。相比之下,长期存活者被排斥的仓鼠心脏显示出大量单核细胞浸润和心肌纤维化,与早期排斥的情况不同。在第2天开始由来氟米特进行治疗,到第6天逆转了这些排斥反应。此外,第2天观察到的同种异体特异性IgM滴度的升高被逆转,并且来氟米特阻止了未经治疗的动物中发生的同种异体特异性IgM向IgG的同种型转换。这些观察结果表明,在无毒剂量下来氟米特有效地控制了协调性异种移植的急性排斥反应,并且来氟米特与环孢素实现了协同免疫抑制作用。

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