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USE OF INHIBITORS OF STRESS GRANULE FORMATION FOR TARGETING THE REGULATION OF IMMUNE RESPONSES

机译:使用应力颗粒形成抑制剂来调节免疫反应

摘要

The mechanisms of tumor escape are numerous, but the immunosuppressive action of coinhibitory molecules has emerged this last decade as the most attractive one for imaging new treatments of cancer. Activation of lymphocytes is indeed regulated by both costimulatory and coinhibitory molecules also called "immune checkpoints". Now the inventors show that T cell activation triggers mRNA and protein expression of stress granule components and more particularly show that immune checkpoint mRNA interact with said stress granules. More importantly, stress granule inhibitors impair expression of immune checkpoint and thus represent an attractive target for targeting the regulation of immune response.
机译:肿瘤逃逸的机制多种多样,但是在最近十年中,共抑制分子的免疫抑制作用已经成为成像新的癌症治疗方法中最有吸引力的分子。淋巴细胞的激活确实受到共刺激分子和共抑制分子(也称为“免疫检查点”)的调节。现在,发明人表明T细胞活化触发应激颗粒组分的mRNA和蛋白表达,并且更具体地表明免疫检查点mRNA与所述应激颗粒相互作用。更重要的是,应激颗粒抑制剂会损害免疫检查点的表达,因此代表了针对免疫应答调节的有吸引力的靶标。

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