Wang R D, Luo Y, Feng Z H, Chen Z C
Department of Medical Molecular Biology, Tongji Medical University, Wuhan.
J Tongji Med Univ. 1990;10(1):43-7. doi: 10.1007/BF02909121.
In this paper, we have described the effects of tumor-derived immunosuppressive factor(s) (TDSF) on interleukin 2 (IL-2) production, on IL-2 responsiveness and on the expression of IL-2 receptors. The results showed that TDSF was able to markedly inhibit the production of IL-2 from PHA-stimulated lymphocytes and IL-2-dependent proliferation of activated lymphocytes, and to partially inhibit the expression of IL-2 receptor. These results suggest that inhibiting IL-2 production and responsiveness may be a major mechanism by which TDSF inhibit T lymphocyte proliferation and other immune responses. That TDSF exerted a very potent inhibiting action on IL-2 responsiveness is especially noticeable if we consider using IL-2 as an immunotherapeutic agent. This may be an important reason why treatment of tumor with IL-2 did not yield satisfactory results so far.
在本文中,我们描述了肿瘤衍生免疫抑制因子(TDSF)对白介素2(IL-2)产生、IL-2反应性以及IL-2受体表达的影响。结果表明,TDSF能够显著抑制PHA刺激的淋巴细胞产生IL-2以及活化淋巴细胞的IL-2依赖性增殖,并部分抑制IL-2受体的表达。这些结果提示,抑制IL-2的产生和反应性可能是TDSF抑制T淋巴细胞增殖和其他免疫反应的主要机制。如果我们考虑将IL-2用作免疫治疗剂,TDSF对IL-2反应性发挥非常有效的抑制作用就尤为值得注意。这可能是迄今为止用IL-2治疗肿瘤未取得满意结果的一个重要原因。