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Cancer neoantigens targeted by adoptive T cell transfer: private no more

机译:过继性T细胞移植靶向的癌症新抗原:不再私有

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Effector T cell responses directed toward cancer neoantigens mediate tumor regression following checkpoint blockade or adoptive T cell immunotherapy, but are generally "private", thus requiring considerable effort for their identification. In this issue of the JCI, Malekzadeh et al. show that a fraction of patients with epithelial cancers mount antigen-specific T cell responses to "hot spot" p53 mutations that in some cases are shared among patients. This work suggests that other genes frequently mutated in human cancer can be immunogenic, thus offering a rapid way to screen for cancer neoantigens that can be targeted by subsequent T cell-based therapies.
机译:针对癌症新抗原的效应 T 细胞反应介导检查点阻断或过继性 T 细胞免疫治疗后的肿瘤消退,但通常是“私密的”,因此需要相当大的努力来识别它们。在本期 JCI 中,Malekzadeh 等人表明,一小部分上皮癌患者对“热点”p53 突变产生抗原特异性 T 细胞反应,在某些情况下,这些突变在患者之间共享。这项工作表明,人类癌症中经常发生突变的其他基因可能具有免疫原性,从而提供了一种快速筛选癌症新抗原的方法,这些新抗原可以通过后续的基于T细胞的疗法进行靶向。

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