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胃肠道癌患者中的淋巴因子激活杀伤细胞(LAK细胞)

Lymphokine activated killer (LAK) cells in patients with gastrointestinal cancer.

作者信息

Monson J R, Ramsden C W, Giles G R, Brennan T G, Guillou P J

机构信息

Department of Surgery, St James's University Hospital, Leeds.

出版信息

Gut. 1987 Nov;28(11):1420-5. doi: 10.1136/gut.28.11.1420.

Abstract

Lymphokine activated killer (LAK) cells are a recently described cellular immune phenomenon with exciting potential for the treatment of tumours arising from solid organs. A comparison of some aspects of LAK cell precursors and LAK cell function was undertaken in 44 control subjects and 44 preoperative patients suffering from gastrointestinal cancer (20 localised and 24 advanced). Lymphokine activated killer cell precursor (natural killer (NK) cell) activity was significantly diminished in patients with advanced tumours (p less than 0.02) as was fully mature LAK cell activity against an NK resistant target cell (p less than 0.012). T-lymphocyte responses were not significantly different between the three groups. The reduced LAK cell generation was associated with a significantly diminished proliferative response of LAK precursors to stimulation with high dose IL-2 in vitro (p less than 0.012). Impaired LAK cell generation may explain the failure of adoptive cellular immunotherapy with LAK cells in some patients with advanced gastrointestinal cancer and prompts the search for means of augmenting this activity in such patients.

摘要

淋巴因子激活的杀伤(LAK)细胞是最近描述的一种细胞免疫现象,在治疗实体器官肿瘤方面具有令人兴奋的潜力。对44名对照受试者和44名患有胃肠道癌的术前患者(20例局限性和24例晚期)的LAK细胞前体和LAK细胞功能的某些方面进行了比较。晚期肿瘤患者的淋巴因子激活的杀伤细胞前体(自然杀伤(NK)细胞)活性显著降低(p<0.02),针对NK抗性靶细胞的完全成熟LAK细胞活性也显著降低(p<0.012)。三组之间的T淋巴细胞反应没有显著差异。LAK细胞生成减少与LAK前体在体外对高剂量IL-2刺激的增殖反应显著降低有关(p<0.012)。LAK细胞生成受损可能解释了一些晚期胃肠道癌患者采用LAK细胞过继性细胞免疫治疗失败的原因,并促使人们寻找增强此类患者这种活性的方法。

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