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FK506和环孢素的免疫抑制作用相同的证据。

Evidence that the immunosuppressive effects of FK506 and cyclosporine are identical.

作者信息

Johansson A, Möller E

机构信息

Department of Clinical Immunology, Huddinge Hospital, Karolinska Institute, Sweden.

出版信息

Transplantation. 1990 Dec;50(6):1001-7. doi: 10.1097/00007890-199012000-00021.

Abstract

The fungal metabolite FK506 was discovered because it shared an important property, the ability to inhibit production of IL-2, with another well-known immunosuppressive fungal metabolite, CsA. FK506 has, since its isolation, also been shown to share other immunosuppressive effects with CsA. This study was performed to further investigate the in vitro immunological properties of FK506, in comparison with and in combination with CsA, to evaluate the plausibility that their mechanisms of action were identical or similar, in spite of their different molecular structures. The ability to inhibit several responses of human peripheral blood lymphocytes to mitogenic and alloantigenic stimulation was explored. Synergistic effects of the two drugs were extensively studied, since this would provide additional information regarding their mechanisms of action. Also, similar immunosuppressive properties would enable the use of the two drugs in combination. We found that FK506 and CsA had very similar mechanisms of action and additive effects were recorded.

摘要

真菌代谢产物FK506的发现是因为它与另一种著名的免疫抑制真菌代谢产物环孢素A(CsA)具有一项重要特性,即抑制白细胞介素-2生成的能力。自FK506分离出来后,还显示它与CsA具有其他免疫抑制作用。进行本研究是为了进一步探究FK506的体外免疫学特性,并与CsA进行比较以及联合使用,以评估尽管它们分子结构不同,但作用机制相同或相似的合理性。研究了抑制人外周血淋巴细胞对有丝分裂原和同种异体抗原刺激的几种反应的能力。对这两种药物的协同作用进行了广泛研究,因为这将提供有关它们作用机制的更多信息。此外,相似的免疫抑制特性将使这两种药物能够联合使用。我们发现FK506和CsA具有非常相似的作用机制,并记录到了相加效应。

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