Department of Pathology, The University of Chicago, Chicago, IL, 60637, USA; David and Etta Jonas Center for Cellular Therapy, The University of Chicago, Chicago, IL, 60637, USA.
Department of Medicine, The University of Chicago, Chicago, IL, 60637, USA.
Curr Opin Immunol. 2022 Feb;74:25-31. doi: 10.1016/j.coi.2021.09.002. Epub 2021 Oct 4.
Certain aspects of experimental tumor models in mice most accurately reflect the biology and immunology of cancer in patients. A survey of experimental cancer immunotherapy papers published in 2020 shows most do not achieve cancer shrinkage although treatment is initiated at an early time point after cancer cell injection, which does not reflect cancer immunotherapy in patients. Even then, few current experimental approaches eradicate the injected malignant cells, most only delay outgrowth. The value of targeting mutation-encoded tumor-specific antigens becomes increasingly evident while problems of finding normal gene-encoded tumor-associated antigens as safe, effective targets persist. It might be time to refocus on realistic experimental settings and truly cancer-specific targets. These antigens are associated with the least risk of side effects.
某些方面的实验性肿瘤模型在小鼠中最能准确反映癌症患者的生物学和免疫学特性。对 2020 年发表的实验性癌症免疫治疗论文进行的调查显示,尽管在癌细胞注射后早期开始治疗,但大多数治疗并不能使肿瘤缩小,这与癌症患者的免疫治疗不符。即便如此,目前很少有实验方法能根除注射的恶性细胞,大多数方法只是延迟了肿瘤的生长。虽然寻找正常基因编码的肿瘤相关抗原作为安全、有效的靶点仍然存在问题,但靶向突变编码的肿瘤特异性抗原的价值变得越来越明显。现在可能是时候重新关注现实的实验环境和真正的肿瘤特异性靶点了。这些抗原与副作用的风险最小相关。