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T淋巴细胞诱导的非T细胞介导的非特异性细胞毒性。I. 诱导机制

T lymphocyte induction of non-T cell-mediated nonspecific cytotoxicity. I. Introduction mechanisms.

作者信息

Mackler B F, O'Neill P A, Meistrich M

出版信息

Eur J Immunol. 1977 Feb;7(2):55-61. doi: 10.1002/eji.1830070202.

Abstract

Mononuclear cells (MNC) from normal humans consistently failed to give nonspecific cytotoxic responses. However, after removal of T cells by sheep erythrocyte (E) rosetting, the remaining non-RFC (rosette-forming cells) now gave significant nonspecific cytotoxic responses against both autologous and allogeneic target cells. Reconstitution experiments with T cell subpopulations failed to suppress these nonspecific non-E-RFC-mediated cytotoxic responses. There was also no evidence to indicate the involvement of antibody in this nonspecific cytotoxicity. The cytotoxic cells were characterized as non-E-rosetting, non-phagocytic, and glass adherent lymphocytes; no evidence of monocyte-macrophage participation was found. The inductive trigger of non-E-RFC-mediated cytotoxicity was found to be soluble factors released by T cells during E-rosette formation at 4 degrees C. Incubation of MNC with horse, marmoset and human erythrocytes under identical conditions failed to trigger cytotoxicity. The incubation of quiescent MNC with E-rosetting supernatants (ERS) induced nonspecific cytotoxic responses equivalent to those mediated by separated non-E-RFC. ERS-activated MNC destroyed both autologous and allogeneic target cells. The ERS supernatants themselves were not cytolytic. These findings suggested that cell separation procedures, and possibly in vivo events, which activate T cells may also induce non-T cell-mediated nonspecific cytotoxicity.

摘要

来自正常人的单核细胞(MNC)始终无法产生非特异性细胞毒性反应。然而,通过绵羊红细胞(E)花环法去除T细胞后,剩余的非花环形成细胞(non-RFC)现在对自体和异体靶细胞都产生了显著的非特异性细胞毒性反应。用T细胞亚群进行的重建实验未能抑制这些非特异性非E-RFC介导的细胞毒性反应。也没有证据表明抗体参与了这种非特异性细胞毒性作用。细胞毒性细胞被鉴定为非E花环形成、非吞噬性且贴壁于玻璃的淋巴细胞;未发现单核细胞-巨噬细胞参与的证据。发现非E-RFC介导的细胞毒性的诱导触发因素是T细胞在4℃形成E花环时释放的可溶性因子。在相同条件下,将MNC与马、狨猴和人类红细胞一起孵育未能触发细胞毒性。将静止的MNC与E花环形成上清液(ERS)孵育可诱导出与分离的非E-RFC介导的非特异性细胞毒性反应相当的反应。ERS激活的MNC可破坏自体和异体靶细胞。ERS上清液本身并无细胞溶解作用。这些发现表明,激活T细胞的细胞分离程序以及可能的体内事件也可能诱导非T细胞介导非特异性细胞毒性。

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