Redelman D, Trefts P E
J Immunol. 1978 Oct;121(4):1532-9.
Xenogeneic rabbit anti-mouse cell-mediated cytotoxic activity could be generated by culturing lymphoid cells from mesenteric lymph nodes (MLN), spleen, or peripheral blood of rabbits primed 2 to 8 weeks earlier with mouse tumor or spleen cells. MLN cells, which provided the best source of activity after being cultured with 5 to 10 X 10(6) mitomycin C-treated mouse spleen cells for 4 to 6 days, produced 30 to 90% specific isotope release after 4 to 7 hr incubation with 15Cr-labeled tumor target cells. Xenogeneic cytotoxic activity was primarily H-2 specific and could not be blocked by immune complexes but was abrogated by treatment with goat anti-rabbit thymocyte serum plus complement (ATS + C) before or after culture. Therefore, the activity appeared to be mediated by cytotoxic T lymphocytes (CTL). Furthermore, ATS without C abrogated cytotoxic activity when included in the CTL assay at concentrations of 5 to 15 microliter/10(7) effector cells. The inhibitory activity of ATS was directed to the rabbit effector population and could be absorbed completely by rabbit thymocytes. Antisera to mouse T cells with comparable cytolytic activity in the presence of C did not inhibit murine allogeneic CTL.
通过培养2至8周前用小鼠肿瘤细胞或脾细胞致敏的兔肠系膜淋巴结(MLN)、脾脏或外周血中的淋巴细胞,可产生异种兔抗小鼠细胞介导的细胞毒性活性。在用5至10×10⁶经丝裂霉素C处理的小鼠脾细胞培养4至6天后,MLN细胞提供了最佳活性来源,在与¹⁵Cr标记的肿瘤靶细胞孵育4至7小时后,产生30%至90%的特异性同位素释放。异种细胞毒性活性主要是H-2特异性的,不能被免疫复合物阻断,但在培养前或培养后用山羊抗兔胸腺细胞血清加补体(ATS + C)处理可消除该活性。因此,该活性似乎由细胞毒性T淋巴细胞(CTL)介导。此外,当在CTL测定中以5至15微升/10⁷效应细胞的浓度加入无补体的ATS时,可消除细胞毒性活性。ATS的抑制活性针对兔效应细胞群体,可被兔胸腺细胞完全吸收。在补体存在下具有相当溶细胞活性的抗小鼠T细胞抗血清不抑制小鼠同种异体CTL。