Nadkarni J J, Jhaver K G, De A K, Soman C S, Nadkarni K S
Immunology Division, Cancer Research Institute, Parel, Bombay, India.
Neoplasma. 1993;40(1):15-20.
Peripheral blood lymphocytes (PBL) and lymph node lymphocytes (LNL) from non-Hodgkin's lymphoma patients were tested for LAK cell cytotoxicity using appropriate targets in a short-term 51chromium-release assay. The results showed a significant depression in LNL-LAK activity suggesting the reduced capacity of LNL to generate LAK cells. LNL-LAK cells demonstrated significantly low percentages of cells expressing CD16, CD56 and CD25 as compared to PBL-LAK of patients and healthy donors. The reduced capacity to generate LAK cells in lymph nodes could be due to the presence of low numbers of NK cells which are thought to be the main precursors of LAK cells. The IL-2 producing ability of lymph node mononuclear cells was found to be significantly higher than that of peripheral blood mononuclear cells from both healthy donors and NHL patients.
在一项短期的51铬释放试验中,使用合适的靶细胞检测了非霍奇金淋巴瘤患者的外周血淋巴细胞(PBL)和淋巴结淋巴细胞(LNL)的LAK细胞细胞毒性。结果显示LNL-LAK活性显著降低,提示LNL产生LAK细胞的能力下降。与患者和健康供体的PBL-LAK相比,LNL-LAK细胞表达CD16、CD56和CD25的细胞百分比显著降低。淋巴结中产生LAK细胞的能力降低可能是由于NK细胞数量较少,而NK细胞被认为是LAK细胞的主要前体。发现来自健康供体和非霍奇金淋巴瘤患者的淋巴结单核细胞产生IL-2的能力显著高于外周血单核细胞。