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环孢素对呼肠孤病毒刺激的小鼠自然杀伤细胞细胞毒性的抑制作用。

Inhibition of reovirus-stimulated murine natural killer cell cytotoxicity by cyclosporine.

作者信息

al-Sheboul S, Crosley D, Steele T A

机构信息

Department of Health Sciences, University of Wisconsin-Milwaukee 53201, USA.

出版信息

Life Sci. 1996;59(20):1675-82. doi: 10.1016/s0024-3205(96)00503-6.

Abstract

Reovirus type 3 is a double-stranded RNA virus that is a potent inducer of murine natural killer (NK) cell cytotoxicity, most likely as a result of virus-induced interferon production. We determined that reovirus was an effective inducer of high levels of NK cytotoxicity. A single injection of cyclosporine (CS), administered concurrently with reovirus or delayed until three days after injecting CS, significantly inhibited NK cytotoxicity. CS significantly suppressed reovirus-induced NK cytotoxicity when added directly to the chromium-release assay. We determined that CS inhibited the ability of murine spleen cells to form conjugates with YAC-1 tumor target cells. Finally, CS was shown to directly inhibit reovirus replication in vitro. Our results demonstrate that CS is an effective inhibitor of reovirus-induced NK cytotoxicity and suggest that inhibition occurs through multiple mechanisms including direct effects on the NK cells and direct inhibition of virus replication.

摘要

3型呼肠孤病毒是一种双链RNA病毒,它是小鼠自然杀伤(NK)细胞细胞毒性的有效诱导剂,很可能是病毒诱导干扰素产生的结果。我们确定呼肠孤病毒是高水平NK细胞毒性的有效诱导剂。与呼肠孤病毒同时注射或延迟至注射环孢素(CS)三天后注射单剂量的环孢素,可显著抑制NK细胞毒性。当直接添加到铬释放试验中时,CS可显著抑制呼肠孤病毒诱导的NK细胞毒性。我们确定CS抑制了小鼠脾细胞与YAC-1肿瘤靶细胞形成结合物的能力。最后,研究表明CS在体外可直接抑制呼肠孤病毒的复制。我们的结果表明,CS是呼肠孤病毒诱导的NK细胞毒性的有效抑制剂,并提示抑制作用通过多种机制发生,包括对NK细胞的直接作用和对病毒复制的直接抑制。

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