使用肾下包膜试验测量抗体依赖,细胞介导的头颈部肿瘤细胞毒性。

R Kau, C Kürten, H Kumazawa, P Koldovsky
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引用次数: 0

摘要

抗体依赖性、细胞介导的细胞毒性(ADCC)研究表明,抗体可以提高淋巴细胞的定位和杀伤能力。我们在裸鼠肾下胶囊实验中测试了提高淋巴因子激活杀伤细胞(LAK)对人肿瘤活性的可能性。肿瘤先在肾包膜间隙生长,再注入效应细胞。在模型实验中,我们使用了M21黑色素瘤和抗黑色素瘤相关抗原GD3的单克隆抗体。与单独LAK相比,该抗体增加了来自健康供体的LAK细胞的肿瘤抑制活性。我们已经能够证明这种方法的临床相关性。对5例肿瘤患者的肿瘤活检材料进行各种单克隆抗体检测,然后选择高活性抗体与患者LAK细胞孵育。经预处理的LAK细胞对实验小鼠肾包膜腔内的自体肿瘤生长有较高的抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of the subrenal capsule assay to measure antibody-dependent, cell-mediated cytotoxicity against head and neck tumors.

Experience with antibody-dependent, cell-mediated cytotoxicity (ADCC) has shown that antibody can increase the localization and killing capacity of lymphocytes. We tested the possibility of improving the activity of lymphokine-activated killer cells (LAK) on human tumor using the subrenal capsule assay in nude mice. The tumors were first grown in the renal capsule space and the effector cells injected later. In the model experiment we used M21 melanoma and monoclonal antibody against melanoma-associated antigen GD3. This antibody increases the tumor inhibitory activity of LAK cells from healthy donors in comparison to LAK alone. We have been able to prove the clinical relevance of such an approach. Tumor bioptic material from five tumor patients was tested with various monoclonal antibodies, following which the highly reactive antibodies were selected and incubated with the patient's LAK cells. Such pretreated LAK cells have a high growth-inhibitory effect on autologous tumor growing in the renal capsule space of the test mice.

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