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口腔癌患者中自然杀伤细胞和淋巴因子激活的杀伤细胞介导的细胞毒性作用

Natural killer and lymphokine-activated killer cell-mediated cytotoxicity in patients with oral cancer.

作者信息

Gangal S G, Tatake R J, Krishnan N, Mukhopadhyaya R, Naik S L, Fakih A R, Rao R S

机构信息

Immunology Division, Cancer Research Institute, Tata Memorial Hospital, Bombay, India.

出版信息

Semin Surg Oncol. 1989;5(5):347-50. doi: 10.1002/ssu.2980050511.

Abstract

Peripheral blood lymphocytes (PBL) from untreated and treated oral cancer patients, lymph node lymphocytes (LNL) from metastatic (met) and nonmetastatic (non-met) lymph nodes, and tumor infiltrating lymphocytes (TIL) were tested for natural killer (NK) and lymphokine activated killer (LAK) cell cytotoxicity using appropriate targets in a short-term chromium release assay. The results showed that while both NK and LAK functions of PBL from oral cancer patients were comparable to those of normal healthy donors, the NK activity of metastatic and nonmetastatic LNL and TIL was highly compromised. On the other hand, potent LAK activity could be generated from all three lymphoid populations. Individual patients showing low NK activity displayed good LAK cytotoxicity, indicating that endogenous cells with low NK potential have adequate ability to respond to interleukin 2 (IL-2). LAK activity tested on autologous tumour targets revealed that TIL were the best source of LAK cells. followed by PBL and LNL.

摘要

采用短期铬释放试验,以合适的靶细胞检测未经治疗和经治疗的口腔癌患者的外周血淋巴细胞(PBL)、转移性(met)和非转移性(non-met)淋巴结的淋巴结淋巴细胞(LNL)以及肿瘤浸润淋巴细胞(TIL)的自然杀伤(NK)和淋巴因子激活的杀伤(LAK)细胞的细胞毒性。结果显示,虽然口腔癌患者PBL的NK和LAK功能与正常健康供者的相当,但转移性和非转移性LNL以及TIL的NK活性严重受损。另一方面,这三种淋巴细胞群体均可产生有效的LAK活性。NK活性低的个体患者表现出良好的LAK细胞毒性,表明NK潜能低的内源性细胞有足够能力对白介素2(IL-2)作出反应。以自体肿瘤靶细胞检测的LAK活性显示,TIL是LAK细胞的最佳来源,其次是PBL和LNL。

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