Taniguchi K, Nomoto K, Kubo C, Nanishi F
Jpn J Exp Med. 1981 Apr;51(2):89-95.
Following priming with alloantigen in vivo, a secondary cytotoxic activity of AKR mice (H-2k) was generated by in vitro stimulation with the same alloantigen. Such secondary effectors could lyse not only targets of a sensitizing haplotype but also third-party targets unrelated to sensitizing or responding cells. Such cross-reactive cytotoxicity of AKR secondary effectors were demonstrated not only by stimulation with C57BL/6 (H-2b) cells but also with C3H/He (H-2k) cells. It was observed that such cross-reactive secondary cytotoxicity was mediated by T lymphocytes, and required protein synthesis in secondary culture. These results suggested the possibility that the antigen receptors on such secondary cytotoxic effector cells have different recognitive specificity from that on primary cytotoxic effector cells.
在体内用同种异体抗原进行预致敏后,通过用相同的同种异体抗原进行体外刺激,诱导产生了AKR小鼠(H-2k)的二次细胞毒性活性。这种二次效应细胞不仅可以裂解致敏单倍型的靶细胞,还可以裂解与致敏或反应细胞无关的第三方靶细胞。AKR二次效应细胞的这种交叉反应性细胞毒性不仅通过用C57BL/6(H-2b)细胞刺激得到证实,还用C3H/He(H-2k)细胞刺激得到了证实。据观察,这种交叉反应性二次细胞毒性是由T淋巴细胞介导的,并且在二次培养中需要蛋白质合成。这些结果提示了这样一种可能性,即这种二次细胞毒性效应细胞上的抗原受体与初次细胞毒性效应细胞上的抗原受体具有不同的识别特异性。