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使用两种免疫抑制药物环孢菌素A和他克莫司来抑制感染猫免疫缺陷病毒的细胞中的病毒复制和凋亡。

The use of two immunosuppressive drugs, cyclosporin A and tacrolimus, to inhibit virus replication and apoptosis in cells infected with feline immunodeficiency virus.

作者信息

Mortola E, Endo Y, Ohno K, Watari T, Tsujimoto H, Hasegawa A

机构信息

Graduate School of Agriculture and Life Sciences, The University of Tokyo, Japan.

出版信息

Vet Res Commun. 1998 Dec;22(8):553-63. doi: 10.1023/a:1006197804888.

Abstract

An in vitro model of acute and chronic infections with feline immunodeficiency virus (FIV) was used to examine the effect of two immunosuppressive agents, cyclosporin A (CsA) and tacrolimus (also known as FK506), on the inhibition of the replication of the virus and of apoptosis. Both drugs significantly suppressed virus production in a dose-dependent manner in acutely and chronically infected cells. The ability of FK506 to inhibit virus replication was much lower than that of CsA, and was accompanied by marked antiproliferative activity. Treatment of infected cells with either CsA or FK506 did not affect the rise of free intracellular Ca2+ but did protect the cells against apoptosis. Thus, the antiviral activity of CsA and FK506 makes these compounds promising candidates for the development of drugs suitable for the treatment of AIDS.

摘要

利用猫免疫缺陷病毒(FIV)急性和慢性感染的体外模型,研究了两种免疫抑制剂环孢菌素A(CsA)和他克莫司(也称为FK506)对病毒复制抑制和细胞凋亡的影响。两种药物均以剂量依赖方式显著抑制急性和慢性感染细胞中的病毒产生。FK506抑制病毒复制的能力远低于CsA,且伴有明显的抗增殖活性。用CsA或FK506处理感染细胞不会影响细胞内游离Ca2+的升高,但能保护细胞免受凋亡。因此,CsA和FK506的抗病毒活性使这些化合物有望成为开发适用于治疗艾滋病药物的候选药物。

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