Jiang Hong, Hegde Samarth, DeNardo David G
Department of Medicine, Washington University School of Medicine, 660 South Euclid Ave., Box 8069, St. Louis, MO, 63110, USA.
ICCE Institute, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Cancer Immunol Immunother. 2017 Aug;66(8):1037-1048. doi: 10.1007/s00262-017-2003-1. Epub 2017 Apr 27.
Tumor-associated fibrosis is characterized by unchecked pro-fibrotic and pro-inflammatory signaling. The components of fibrosis including significant numbers of cancer-associated fibroblasts, dense collagen deposition, and extracellular matrix stiffness, are well appreciated regulators of tumor progression but may also be critical regulators of immune surveillance. While this suggests that the efficacy of immunotherapy may be limited in highly fibrotic cancers like pancreas, it also suggests a therapeutic opportunity to target fibrosis in these tumor types to reawaken anti-tumor immunity. This review discusses the mechanisms by which fibrosis might subvert tumor immunity and how to overcome these mechanisms.
肿瘤相关纤维化的特征是促纤维化和促炎信号不受控制。纤维化的组成成分,包括大量癌症相关成纤维细胞、致密的胶原沉积和细胞外基质硬度,是肿瘤进展的公认调节因子,但也可能是免疫监视的关键调节因子。虽然这表明免疫疗法在胰腺癌等高度纤维化癌症中的疗效可能有限,但也提示了在这些肿瘤类型中靶向纤维化以重新唤醒抗肿瘤免疫的治疗机会。本综述讨论了纤维化可能颠覆肿瘤免疫的机制以及如何克服这些机制。