Terasaka R, Himeno K, Shiraishi M, Nomoto K
Jpn J Exp Med. 1981 Apr;51(2):75-80.
Cytotoxic activity was detected by the 51 CR-release test in peritoneal exudate (PE) cells of mice immunized with rat lymphocytes 5 days previously, but not in their spleen or lymph node cells. This activity appeared to be exerted by cytotoxic T cells, which had the same characteristics as those for allogeneic systems in respect to antigen specificity and time course. An intraperitoneal booster with rat lymphocytes 2 days before the assay effectively enhanced the cytotoxic activity of PE cells. When mice were immunized with rat lymphocytes subcutaneously or intravenously, cytotoxic activity was scarcely detected in PE cells. However, significant activity was detected in PE cells when the immunized mice were injected intraperitoneally with proteose peptone 2 days before the assay.
采用51Cr释放试验检测5天前用大鼠淋巴细胞免疫的小鼠腹腔渗出液(PE)细胞的细胞毒性活性,但其脾脏或淋巴结细胞中未检测到该活性。这种活性似乎是由细胞毒性T细胞发挥的,其在抗原特异性和时间进程方面与同种异体系统的细胞毒性T细胞具有相同的特征。在检测前2天腹腔注射大鼠淋巴细胞进行加强免疫可有效增强PE细胞的细胞毒性活性。当小鼠经皮下或静脉注射大鼠淋巴细胞免疫时,在PE细胞中几乎检测不到细胞毒性活性。然而,在检测前2天给免疫小鼠腹腔注射蛋白胨时,在PE细胞中检测到了显著的活性。