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体内肿瘤免疫诱导机制的研究。IV. 正常腹膜巨噬细胞及其培养上清液对体外继发性细胞介导细胞毒性反应生成的增强作用。

Studies of the mechanisms for the induction of in vivo tumor immunity. IV. Enhancement of the in vitro generation of secondary cell-mediated cytotoxic response by normal peritoneal macrophages and their culture supernatants.

作者信息

Igarashi T, Rodrigues D, Ting C C

出版信息

J Immunol. 1979 Apr;122(4):1519-27.

PMID:156217
Abstract

The effect of macrophages on the induction of the cell-mediated cytotoxicity against a leukemia in a syngeneic system was investigated. The addition of exogenous peritoneal cells from normal C57BL/6 MIce enhanced the in vitro secondary cell-mediated cytotoxic response of both spleen and lymph node cells as responding cells against syngeneic FBL-3 leukemia. Peritoneal phagocytic macrophages seemed to be responsible for the enhancement. No inhibitory effect was demonstrated by the addition of peritoneal macrophages at a concentration as high as 20%, whereas the primary cytotoxic allograft response was significantly suppressed. In the present studies, there was no absolute restriction of macrophage-T cell interaction by an H-2 barrier. Supernatants of peritoneal macrophage cultures also enhanced this cell-mediated cytotoxic response. There was no difference between the effects of syngeneic or allogeneic peritoneal macrophage culture supernatants.

摘要

研究了巨噬细胞在同基因系统中对诱导针对白血病的细胞介导细胞毒性的作用。添加来自正常C57BL/6小鼠的外源性腹腔细胞可增强脾细胞和淋巴结细胞作为针对同基因FBL-3白血病的反应细胞的体外二次细胞介导细胞毒性反应。腹腔吞噬巨噬细胞似乎是这种增强作用的原因。添加浓度高达20%的腹腔巨噬细胞未显示出抑制作用,而原发性细胞毒性同种异体移植反应则受到显著抑制。在本研究中,H-2屏障对巨噬细胞与T细胞的相互作用没有绝对限制。腹腔巨噬细胞培养上清液也增强了这种细胞介导的细胞毒性反应。同基因或异基因腹腔巨噬细胞培养上清液的作用没有差异。

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