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一种针对介导黏附的蛋白gp 90(CD18)的单克隆抗体对自然杀伤细胞细胞毒性的抑制作用。

Inhibition of natural killer cell cytotoxicity by a monoclonal antibody directed against adhesion-mediating protein gp 90 (CD18).

作者信息

Axberg I, Ramstedt U, Patarroyo M, Beatty P, Wigzell H

机构信息

Department of Immunology, Karolinska Institute Stockholm, Sweden.

出版信息

Scand J Immunol. 1987 Nov;26(5):547-54. doi: 10.1111/j.1365-3083.1987.tb02288.x.

Abstract

Contact is required between the effector natural killer (NK) or cytotoxic killer T cell and its corresponding target in order for efficient lysis to occur. Several surface molecules of different types are involved in this process. Here we could show that Fab fragments from a murine monoclonal antibody reacting with gp 90, the human leucocyte common antigen CD18, are extremely efficient in blocking human NK of killer T cells, regardless of whether the target has or does not have the antigen. In contrast, no impact of the antibody was observed when the effector cells were of murine origin, again regardless of whether the target cell did or did not display the leucocyte common antigen. The inhibition could be shown to occur at the level of blockage of target-conjugate formation. This means that the functional display of effector/target gp 90 on the effector but not the target cell is necessary for efficient lysis to occur both in NK and killer T cell systems.

摘要

为了实现高效裂解,效应自然杀伤(NK)细胞或细胞毒性杀伤性T细胞与其相应靶标之间需要接触。该过程涉及几种不同类型的表面分子。在这里我们可以证明,来自与gp 90(人类白细胞共同抗原CD18)反应的鼠单克隆抗体的Fab片段,在阻断杀伤性T细胞的人类NK细胞方面极其有效,无论靶标是否具有该抗原。相比之下,当效应细胞源自小鼠时,未观察到抗体的影响,同样无论靶细胞是否显示白细胞共同抗原。可以证明这种抑制发生在靶标-共轭物形成的阻断水平。这意味着,效应细胞而非靶细胞上效应器/靶标gp 90的功能性展示,对于NK细胞和杀伤性T细胞系统中高效裂解的发生都是必要的。

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