Carroll P G, DeWolf W C
J Immunol. 1983 Aug;131(2):1007-10.
Four human teratocarcinoma (HT) cell lines were studied as a class of targets for natural (NK) and activated (AK) lymphocyte-mediated cytotoxicity. NK cells were found to be ineffective in lysing 51chromium-labeled HT targets. In contrast, alloactivated and mitogen-activated AK cells were highly cytotoxic for HT. The specificity of AK-mediated HT lysis was investigated by cold target competition experiments. The results showed that the target was shared by all HT lines tested but was not MHC related and was not present on lymphoblastoid cells (LBL) or on resting or activated normal lymphocytes. The demonstrated presence of unique fetal antigens on HT may provide an informative model for the study of AK target specificity and its functional relationship to differentiation.
研究了四种人畸胎癌(HT)细胞系,作为天然(NK)和活化(AK)淋巴细胞介导的细胞毒性的一类靶标。发现NK细胞在裂解51铬标记的HT靶标方面无效。相比之下,同种异体活化和丝裂原活化的AK细胞对HT具有高度细胞毒性。通过冷靶竞争实验研究了AK介导的HT裂解的特异性。结果表明,该靶标为所有测试的HT细胞系所共有,但与主要组织相容性复合体(MHC)无关,且不存在于淋巴母细胞系(LBL)或静止或活化的正常淋巴细胞上。HT上独特胎儿抗原的证实存在可能为研究AK靶标特异性及其与分化的功能关系提供一个有益的模型。