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人T淋巴细胞的激活。III. 抗T3抗原抗体或钙离子载体对细胞毒性T细胞克隆中旁观者细胞毒性的触发作用。

Activation of human T lymphocytes. III. Triggering of bystander cytotoxicity in cytotoxic T cell clones by antibodies against the T3 antigen or by a calcium ionophore.

作者信息

Schrezenmeier H, Kurrle R, Wagner H, Fleischer B

出版信息

Eur J Immunol. 1985 Oct;15(10):1019-24. doi: 10.1002/eji.1830151011.

Abstract

The role of T cell differentiation antigens in antigen-specific and nonspecific cytotoxicity by human cytotoxic T lymphocyte (CTL) clones was investigated. In contrast to other reports, several monoclonal antibodies (mAb) against the T3 antigen only marginally blocked antigen-specific cytotoxicity at high concentrations but induced cytotoxicity against third party cells at concentrations from 10 to 0.001 micrograms/ml. Susceptibility to anti-T3-induced lysis was variable but was found with all target cells. Incubation of CTL with anti-T3 mAb even led to self-destruction of the CTL. The effect was independent of the presence of Fc receptors on the target cell and could be obtained with F(ab')2 fragments of the antibody as well. Only activated but not resting T cells could be induced to lyse by anti-T3. Furthermore, this type of bystander killing of target cells could also be induced by the Ca2+ ionophore A23187. Antibodies against the T8 differentiation antigen inhibited antigen-specific, oxidation-induced and anti-T3-induced cytotoxicity by T8+ CTL clones, whereas triggering by the ionophore A23187 was not inhibited. These results show that undirected killing can be triggered in CTL by activating a transducing molecule directly without involving the antigen receptor. Since this triggering of the lethal hit can still be inhibited by mAb against the T8 molecule, the T8 molecule probably has a regulatory role in a late phase of CTL triggering.

摘要

研究了T细胞分化抗原在人细胞毒性T淋巴细胞(CTL)克隆的抗原特异性和非特异性细胞毒性中的作用。与其他报道相反,几种抗T3抗原的单克隆抗体(mAb)在高浓度时仅轻微阻断抗原特异性细胞毒性,但在浓度为10至0.001微克/毫升时可诱导对第三方细胞的细胞毒性。对抗T3诱导裂解的敏感性各不相同,但在所有靶细胞中均有发现。CTL与抗T3 mAb孵育甚至导致CTL自身破坏。该效应与靶细胞上Fc受体的存在无关,用抗体的F(ab')2片段也可获得相同结果。只有活化的而非静止的T细胞可被抗T3诱导裂解。此外,这种旁观者杀伤靶细胞的类型也可由Ca2+离子载体A23187诱导。抗T8分化抗原的抗体抑制T8+ CTL克隆的抗原特异性、氧化诱导和抗T3诱导的细胞毒性,而离子载体A23187引发的细胞毒性未被抑制。这些结果表明,通过直接激活转导分子而不涉及抗原受体,可在CTL中引发无定向杀伤。由于针对T8分子的mAb仍可抑制这种致死性打击的引发,T8分子可能在CTL引发的后期具有调节作用。

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