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New insights into IL-12-mediated tumor suppression

机译:IL-12介导的肿瘤抑制的新见解

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During the past two decades, interleukin-12 (IL-12) has emerged as one of the most potent cytokines in mediating antitumor activity in a variety of preclinical models. Through pleiotropic effects on different immune cells that form the tumor microenvironment, IL-12 establishes a link between innate and adaptive immunity that involves different immune effector cells and cytokines depending on the type of tumor or the affected tissue. The robust antitumor response exerted by IL-12, however, has not yet been successfully translated into the clinics. The majority of clinical trials involving treatment with IL-12 failed to show sustained antitumor responses and were associated to toxic side effects. Here we discuss the therapeutic effects of IL-12 from preclinical to clinical studies, and will highlight promising strategies to take advantage of the antitumor activity of IL-12 while limiting adverse effects.
机译:在过去的二十年中,白介素12(IL-12)在各种临床前模型中已成为介导抗肿瘤活性的最有效细胞因子之一。通过对形成肿瘤微环境的不同免疫细胞的多效作用,IL-12在先天免疫和适应性免疫之间建立了联系,后者取决于肿瘤或受影响组织的类型,涉及不同的免疫效应细胞和细胞因子。但是,IL-12产生的强大的抗肿瘤反应尚未成功地应用于临床。涉及用IL-12治疗的大多数临床试验未能显示出持续的抗肿瘤反应,并且与毒性副作用相关。在这里,我们讨论从临床前到临床研究中IL-12的治疗作用,并将重点介绍利用IL-12的抗肿瘤活性同时限制不良反应的有前途的策略。

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