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在经环孢素处理的感染小鼠中,流感病毒特异性T细胞无法降低肺部病毒滴度。

Influenza virus-specific T cells fail to reduce lung virus titres in cyclosporin-treated, infected mice.

作者信息

Schiltknecht E, Ada G L

出版信息

Scand J Immunol. 1985 Jul;22(1):99-103. doi: 10.1111/j.1365-3083.1985.tb01864.x.

Abstract

Cyclosporin A (CsA) inhibited the function(s) of transferred influenza-specific K,D-restricted cytotoxic T cells, which led to clearance of virus in the lungs of influenza virus-infected mice. CsA had no effect on the migration of the transferred cells to the lungs. The pattern of migration and the number of cells recovered from the lungs were similar when cells were transferred into normal, untreated, infected or CsA-treated, infected mice. CsA had no effect on the in vitro expression of cytotoxic activity by the K,D-restricted cytotoxic T cells. These findings strongly suggest that the in vivo clearance of influenza virus by K,D-restricted cytotoxic T cells involves a lymphokine mechanism.

摘要

环孢菌素A(CsA)抑制了转移的流感特异性K、D限制性细胞毒性T细胞的功能,这导致流感病毒感染小鼠肺部的病毒清除。CsA对转移细胞向肺部的迁移没有影响。当将细胞转移到正常、未处理、感染或经CsA处理的感染小鼠体内时,细胞的迁移模式和从肺部回收的细胞数量相似。CsA对K、D限制性细胞毒性T细胞的体外细胞毒性活性表达没有影响。这些发现强烈表明,K、D限制性细胞毒性T细胞对流感病毒的体内清除涉及一种淋巴因子机制。

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