Suppr超能文献

用环孢素A、他克莫司(FK506)或西罗莫司(雷帕霉素)免疫抑制的小鼠中的侵袭性曲霉病

Invasive aspergillosis in mice immunosuppressed with cyclosporin A, tacrolimus (FK506), or sirolimus (rapamycin).

作者信息

High K P, Washburn R G

机构信息

Department of Internal Medicine, Bowman Gray School of Medicine, Winston-Salem, North Carolina 27157-1042, USA.

出版信息

J Infect Dis. 1997 Jan;175(1):222-5. doi: 10.1093/infdis/175.1.222.

Abstract

Cyclosporin A, tacrolimus, and sirolimus are immunosuppressive agents initially described as antifungal compounds with different activities for Aspergillus species. The outcome of invasive aspergillosis in mice treated with each agent was investigated in outbred CD-1 mice. Immunosuppressant or vehicle alone was administered from days -1 to +14. Mice were infected on day 0 with resting Aspergillus conidia via lateral tail vein injection. Survival was significantly greater with most regimens than for mice treated with cyclosporin A (100 mg/kg/day; median survival, 3 days): tacrolimus, 1 mg/kg/day (6.5 days, P = .003); sirolimus, 1 or 10 mg/kg/day (7.5 and 9.5 days, respectively; P = .002 and .0001); and vehicle alone (6.5 days, P = .001). However, mice treated with 10 mg/kg/day of tacrolimus survived a median of 4.5 days (P = .25). Survival in the 10-mg sirolimus group did not differ from that of mice given vehicle alone (P = .55). Histologic evaluation suggested the improved survival with tacrolimus and sirolimus may be due in part to direct anti-Aspergillus activity.

摘要

环孢素A、他克莫司和西罗莫司是免疫抑制剂,最初被描述为对曲霉菌具有不同活性的抗真菌化合物。在远交系CD-1小鼠中研究了用每种药物治疗的侵袭性曲霉病小鼠的结局。从第-1天至第+14天单独给予免疫抑制剂或赋形剂。在第0天通过侧尾静脉注射用静止的曲霉分生孢子感染小鼠。大多数治疗方案的生存率显著高于用环孢素A治疗的小鼠(100mg/kg/天;中位生存期,3天):他克莫司,1mg/kg/天(6.5天,P = 0.003);西罗莫司,1或10mg/kg/天(分别为7.5天和9.5天;P = 0.002和0.0001);以及单独给予赋形剂(6.5天,P = 0.001)。然而,用10mg/kg/天他克莫司治疗的小鼠中位生存期为4.5天(P = 0.25)。10mg西罗莫司组的生存率与单独给予赋形剂的小鼠无差异(P = 0.55)。组织学评估表明,他克莫司和西罗莫司改善生存率可能部分归因于直接的抗曲霉活性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验