Falk W, Männel D N, Dröge W
J Immunol. 1983 May;130(5):2214-8.
The dependency of induction of T cell cytotoxicity on lymphokines was studied. 1 X 10(5) nylon wool-purified thymic lymphocytes or 10(4) spleen cells were cultured with TNP-haptenated syngeneic UV-irradiated spleen cells in the presence of a variety of lymphokine preparations. Concanavalin A-induced spleen cell supernatants mediated strong cytotoxic responses in this system. Three other preparations, namely, a partially purified IL 2 preparation from PMA-stimulated EL-4 thymoma cells, a Con A-induced spleen cell supernatant that was absorbed with an IL 2-dependent cell line, and a Con A-induced supernatant that was dialyzed at pH 2 were all ineffective in mediating a cytotoxic response. In reconstitution experiments, cytotoxic responses were only obtained when either the absorbed preparation or the pH 2-treated preparation was mixed with the IL 2 preparation from EL-4 cells. No reconstitution occurred after mixing of the absorbed with the pH 2-treated preparation. pH 2 treatment of the absorbed preparation did not abolish its synergistic effect when added to the IL 2 preparation from EL-4 cells. These results led to the conclusion that activation of cytotoxic lymphocyte precursors requires at least two other lymphokines in addition to IL 2. One T cell cytotoxicity-inducing factor (TCF1) remained in Con A-induced supernatants after absorption with IL 2 receptor-bearing T cell line cells. It was pH 2-resistant and was not found in EL-4 supernatants. A second T cell cytotoxicity-inducing factor (TCF2) was pH 2-sensitive and was found in Con A-induced spleen cell supernatants as well as in interferon-free supernatants of PMA-stimulated EL-4 cells. This activity co-purified with IL 2. It was absorbed by the IL 2-dependent T cell line together with IL 2. IL 2 differs from TCF2 since it is pH 2-resistant.
研究了T细胞细胞毒性诱导对淋巴因子的依赖性。将1×10⁵经尼龙毛纯化的胸腺淋巴细胞或10⁴脾细胞与经TNP半抗原处理的同基因紫外线照射脾细胞在多种淋巴因子制剂存在的情况下进行培养。刀豆球蛋白A诱导的脾细胞上清液在该系统中介导了强烈的细胞毒性反应。其他三种制剂,即来自PMA刺激的EL-4胸腺瘤细胞的部分纯化的IL-2制剂、用IL-2依赖细胞系吸附的刀豆球蛋白A诱导的脾细胞上清液以及在pH 2下透析的刀豆球蛋白A诱导的上清液,在介导细胞毒性反应方面均无效。在重组实验中,只有当吸附制剂或pH 2处理制剂与来自EL-4细胞的IL-2制剂混合时,才获得细胞毒性反应。吸附制剂与pH 2处理制剂混合后未发生重组。当将吸附制剂加入来自EL-4细胞的IL-2制剂中时,pH 2处理并未消除其协同作用。这些结果得出结论,细胞毒性淋巴细胞前体的激活除IL-2外至少还需要另外两种淋巴因子。一种T细胞细胞毒性诱导因子(TCF1)在用携带IL-2受体的T细胞系细胞吸附后仍保留在刀豆球蛋白A诱导的上清液中。它对pH 2有抗性,在EL-4上清液中未发现。第二种T细胞细胞毒性诱导因子(TCF2)对pH 2敏感,在刀豆球蛋白A诱导的脾细胞上清液以及PMA刺激的EL-4细胞的无干扰素上清液中均有发现。该活性与IL-2共纯化。它与IL-2一起被IL-2依赖的T细胞系吸附。IL-2与TCF2不同,因为它对pH 2有抗性。