肿瘤相关抗原是免疫系统的细胞因子诱导剂和低反应性因子。

A D Inglot, F Gelder, J A Georgiades
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引用次数: 10

摘要

我们研究了导致慢性疾病患者免疫系统抑制的可能机制。肿瘤细胞产生的蛋白质释放到循环中,如肿瘤相关抗原,可能在免疫系统瘫痪前的过程中起重要作用。为了验证这一假设,使用了以下肿瘤相关抗原:AFP, OFP, CA-125, CA-50和CA-19-9。它们的作用是通过调节脐带血淋巴细胞和外周血白细胞中细胞因子的产生来评估的,这些细胞因子来自于接受过初乳素(一种细胞因子诱导剂)治疗的成年患者。以PHA、LPS和初乳杆菌素为阳性对照。每一种抗原均以剂量依赖性方式诱导IFN、TNF α和IL-6。这些细胞因子都不是由细胞自发释放的。从这些实验中产生的数据表明,肿瘤相关抗原以与LPS或初乳蛋白相似的方式诱导1型细胞因子。然而,从接受初乳蛋白治疗的患者身上提取的淋巴细胞显示,与初乳蛋白治疗的患者一样,产生1型细胞因子的能力逐渐丧失。对抗原反应能力的丧失可能是导致免疫耐受的现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor-associated antigens are cytokine inducers and hyporeactivity factors to the immune system.

We investigated possible mechanisms leading to the inhibition of the immune system in people with chronic disorders. Tumor cell produce protein released into the circulation, such as tumor associated antigens, may play an important role in processes preceding paralysis of the immune system. To test this hypothesis the following tumor associated antigens were used: AFP, OFP, CA-125, CA-50 and CA-19-9. Their role was assessed by modulating cytokine production in cord blood lymphocytes and peripheral white blood cells obtained from grown population of patients treated with colostrinin, an cytokine inducer. PHA, LPS and colostrinin were used as positive control in those essays. Each antigen tested individually induced IFN, TNF alpha and IL-6 in dose dependent fashion. None of the tested cytokines were spontaneously released by the cells. Data generated from these experiments indicated that tumor associated antigens are inducing type 1 cytokines in similar fashion as LPS or colostrinin. However, lymphocytes taken from patients undergoing therapy with colostrinin revealed progressive loss capability to produce type 1 cytokines as they did in case of colostrinin. The loss of the capability to respond to antigen may represent phenomenon leading to immune tolerance.

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