Vánky F, Klein E
Department of Tumor Biology, Karolinska Institute, Stockholm, Sweden.
Semin Cancer Biol. 1991 Feb;2(1):55-62.
Expression of class I antigens on ex-vivo tumor cells was found to be required for their recognition by autologous blood lymphocytes in vitro. Lymphocyte stimulation (auto-tumor stimulation ATS) in mixed lymphocyte tumor cell cultures (MLTC) and cytolysis in short term assays (autologous lymphocyte-mediated cytotoxicity ALC) were positive with cells of a proportion of sarcoma and carcinoma patients. In addition to the class I antigens, these tumors also carried the adhesion molecule ICAM-1. Monoclonal antibodies (MAb) to the MHC class I, but not to class II antigens inhibited lymphocyte proliferation in the MLTC and lysis of tumor cells in the ALC tests. In a proportion of originally negative or low expressor tumors, in vitro treatment with Interferon gamma and tumor necrosis factor alpha induced the expression of class I antigens and/or ICAM-1. In the MLTC the cytokine treated tumor cells stimulated the blood lymphocytes and generated cytotoxic effectors which reacted also with the untreated tumor cells.
研究发现,体外肿瘤细胞上I类抗原的表达是其被自体血淋巴细胞识别所必需的。在混合淋巴细胞肿瘤细胞培养(MLTC)中,淋巴细胞刺激(自体肿瘤刺激ATS)以及短期试验中的细胞溶解(自体淋巴细胞介导的细胞毒性ALC)在部分肉瘤和癌患者的细胞中呈阳性。除I类抗原外,这些肿瘤还携带黏附分子ICAM-1。针对MHC I类而非II类抗原的单克隆抗体(MAb)可抑制MLTC中的淋巴细胞增殖以及ALC试验中肿瘤细胞的裂解。在部分原本呈阴性或低表达的肿瘤中,用γ干扰素和肿瘤坏死因子α进行体外处理可诱导I类抗原和/或ICAM-1的表达。在MLTC中,经细胞因子处理的肿瘤细胞刺激血淋巴细胞并产生细胞毒性效应细胞,这些效应细胞也可与未处理的肿瘤细胞发生反应。