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癌症患者抑制性细胞活性缺陷:免疫调节缺陷。

Defective suppressor cell activity in cancer patients: a defect in immune regulation.

作者信息

Hubbard G W, Wanebo H, Fukuda M, Pace R

出版信息

Cancer. 1981 May 1;47(9):2177-84. doi: 10.1002/1097-0142(19810501)47:9<2177::aid-cncr2820470912>3.0.co;2-9.

Abstract

Although suppressor cells appear to be involved in the normal regulatory mechanism of the lymphoid system, they are also considered to have a role in the immunosuppression of certain malignancies. Suppressor activity of lymphocytes can be reproducibly measured by use of the mixed lymphocyte culture-mitogen interaction (MLC-M) in which the stimulating cell either is in the basal state or has been induced by Concanavalin A. This yields a quantitative measure of resting suppressor cell activity as well as the maximum generation of suppressor activity as induced by Con A. This test was performed, using autologous and allogenic cell combinations in a group of 13 cancer patients and 18 normal controls. Normal lymphocytes activated by Con A in 48-hour lymphocyte cultures significantly decreased the mitogenic response of lymphocytes from healthy, male donors to phytohemagglutinin (PHA), Con A, and Pokeweed mitogen (PWM) in both autologous and homologous systems. In contrast, Con A activated lymphocytes from cancer patients demonstrated diminished suppressor activity compared with controls in autologous (P less than 0.01), and allogenic (P less than 0.005) systems. There was a correlation between the degree of immunosuppression and suppressor cell activation: i.e., the patients most depressed generally had the lowest suppressor cell activation. Untreated lymphocytes from cancer patients also exerted suppressive effects on normal lymphocyte responses, suggesting an increased resting level of suppressor cells. These data suggest that in addition to having depressed cellular immune responses, cancer patients frequently have reduced capability to generate suppressor cell activity, which implies a generalized defect in this aspect of immune regulation.

摘要

尽管抑制细胞似乎参与了淋巴系统的正常调节机制,但它们也被认为在某些恶性肿瘤的免疫抑制中发挥作用。淋巴细胞的抑制活性可以通过混合淋巴细胞培养-丝裂原相互作用(MLC-M)来重复性地测量,其中刺激细胞要么处于基础状态,要么已被刀豆蛋白A诱导。这产生了静止抑制细胞活性的定量测量以及由Con A诱导的抑制活性的最大生成量。该测试使用了13名癌症患者和18名正常对照的自体和异体细胞组合进行。在48小时的淋巴细胞培养中,被Con A激活的正常淋巴细胞在自体和同源系统中均显著降低了健康男性供体淋巴细胞对植物血凝素(PHA)、Con A和商陆有丝分裂原(PWM)的促有丝分裂反应。相比之下,在自体(P小于0.01)和异体(P小于0.005)系统中,癌症患者被Con A激活的淋巴细胞与对照相比显示出抑制活性降低。免疫抑制程度与抑制细胞激活之间存在相关性:即,免疫抑制最严重的患者通常抑制细胞激活水平最低。癌症患者未经处理的淋巴细胞也对正常淋巴细胞反应产生抑制作用,表明抑制细胞的静止水平增加。这些数据表明,癌症患者除了细胞免疫反应受到抑制外,通常产生抑制细胞活性的能力也降低,这意味着在免疫调节的这方面存在普遍缺陷。

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