Laboratory of Translational Immunology and.
Flow Cytometry Core, Humanitas Clinical and Research Center, Rozzano, Milan, Italy.
J Clin Invest. 2019 Mar 1;129(3):949-951. doi: 10.1172/JCI126295. Epub 2019 Feb 4.
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.
效应 T 细胞针对肿瘤新抗原的反应介导了检查点阻断或过继性 T 细胞免疫疗法后的肿瘤消退,但通常是“私人的”,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,一部分上皮癌患者对“热点”p53 突变产生了抗原特异性 T 细胞反应,在某些情况下,这些突变在患者之间是共享的。这项工作表明,人类癌症中经常发生突变的其他基因也具有免疫原性,因此提供了一种快速筛选可被后续基于 T 细胞的治疗靶向的肿瘤新抗原的方法。