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通过放射性同位素技术在体外检测针对肿瘤特异性抗原的细胞毒性细胞免疫。

In vitro detection of cytotoxic cellular immunity against tumor-specific antigens by a radioisotopic technique.

作者信息

Jagarlamoody S M, Aust J C, Tew R H, McKhann C F

出版信息

Proc Natl Acad Sci U S A. 1971 Jun;68(6):1346-50. doi: 10.1073/pnas.68.6.1346.

Abstract

[(3)H]Thymidine-labeled tumor cells are used to evaluate the cytotoxic cellular immune response against tumor-specific antigens; the loss of label due to destruction and detachment of target cells from the surface of the culture vessel is measured. Spleen cells from mice immunized against Moloney virus-induced rhabdomyosarcoma specifically destroyed the sarcoma cells, while cells from normal syngeneic mice did not. Peripheral blood lymphocytes from patients with malignant tumors were specifically cytotoxic to autologous tumor cells and to allogeneic tumor cells histopathologically identical to the autologous tumor, but not to autologous nonmalignant fibroblasts, or to allogeneic tumor cells from a histologically dissimilar tumor. Serum from the same patients specifically protected autologous tumor cells from lymphocyte cytotoxicity. This serum-mediated protection of tumor cells against autologous cellular immunocytotoxicity also extended to histologically identical allogeneic tumor cells. Cross-reactivity of anti-tumor cellular immunocytotoxicity in vitro, and its "blocking" by autologous serum, strongly suggest the presence of common tumor antigens. The antagonism demonstrated in vitro between serum and cellular immunity may explain the continued growth of malignant tumors in the face of demonstrable cellular immunity.

摘要

用[³H]胸腺嘧啶核苷标记的肿瘤细胞来评估针对肿瘤特异性抗原的细胞毒性细胞免疫反应;通过测量由于靶细胞从培养容器表面破坏和脱离导致的标记物损失来进行评估。用莫洛尼病毒诱导的横纹肌肉瘤免疫的小鼠的脾细胞能特异性地破坏肉瘤细胞,而来自同基因正常小鼠的细胞则不能。恶性肿瘤患者的外周血淋巴细胞对自体肿瘤细胞以及组织病理学上与自体肿瘤相同的同种异体肿瘤细胞具有特异性细胞毒性,但对自体非恶性成纤维细胞或来自组织学上不同肿瘤的同种异体肿瘤细胞没有细胞毒性。同一患者的血清能特异性地保护自体肿瘤细胞免受淋巴细胞的细胞毒性作用。这种血清介导的肿瘤细胞对自体细胞免疫细胞毒性的保护作用也扩展到了组织学上相同的同种异体肿瘤细胞。体外抗肿瘤细胞免疫细胞毒性的交叉反应性及其被自体血清“阻断”,强烈提示存在共同的肿瘤抗原。血清和细胞免疫在体外表现出的拮抗作用可能解释了在存在可证实的细胞免疫的情况下恶性肿瘤仍持续生长的现象。

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