Heininger D, Touton M, Chakravarty A K, Clark W R
J Immunol. 1976 Dec;117(6):2175-80.
The requirements for activation of cytotoxic function in mouse T lymphocytes were investigated. Initial generation of cytotoxicity in normal lymphocytes was equal in magnitude with either Con A or specific alloantigen, and in either case required DNA synthesis. Cytotoxic function in MLC-primed cells could also be regenerated by Con A, the magnitude and target specificity of the cytotoxicity thus generated being indistinguishable from that recalled by specific alloantigen. Cytotoxicity could also be regenerated by third party-stimulating cells; however, the cytotoxicity evoked by third party cells was always specific only for target cells of the original stimulating cell H-2 genotype. The data presented suggest that there are a number of ways to activate cytotoxicity in effector T cells, and are most consistent with a model for T cell triggering that minimizes a strict informational function of antigen-receptor interactions.
对小鼠T淋巴细胞中细胞毒性功能激活的要求进行了研究。正常淋巴细胞中细胞毒性的初始产生,无论是用刀豆蛋白A(Con A)还是特异性同种异体抗原,其程度都是相同的,并且在这两种情况下都需要DNA合成。混合淋巴细胞培养(MLC)致敏细胞中的细胞毒性功能也可以被Con A再生,由此产生的细胞毒性的程度和靶标特异性与由特异性同种异体抗原召回的细胞毒性无法区分。细胞毒性也可以被第三方刺激细胞再生;然而,第三方细胞诱发的细胞毒性总是仅对原始刺激细胞H-2基因型的靶细胞具有特异性。所呈现的数据表明,有多种方法可以激活效应T细胞中的细胞毒性,并且与一种使抗原受体相互作用的严格信息功能最小化的T细胞触发模型最为一致。