Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27559, USA; Department of Pharmaceutics, Collage of Pharmacy, Shandong University, Jinan, 250012, PR China.
Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, PR China.
Cancer Lett. 2019 Apr 28;448:31-39. doi: 10.1016/j.canlet.2019.01.032. Epub 2019 Feb 5.
Solid tumors especially desmoplastic tumors are complex organ-like structures. Tumor-associated fibroblasts (TAFs), one type of the stromal cells, support the initiation, progression, and metastasis of carcinomas. TAFs also contribute to immunosuppressive tumor microenvironment (TME) and hinder T lymphocytes in killing tumors. Here, the role of TAFs in TME is discussed. In specific, TAFs form barriers for the penetration of T lymphocytes. TAFs also act as negative regulators for T lymphocytes. These findings suggest that targeting TAFs is a promising strategy for improving cancer immunotherapy. Our previous studies have indicated the ability of therapeutic nanoparticles to distribute into, and deplete or inactivate TAFs. This approach is discussed in the context of developing specific and effective immunotherapies for cancer.
实体瘤,尤其是促结缔组织增生性肿瘤,是一种复杂的器官样结构。肿瘤相关成纤维细胞(TAFs)是一种基质细胞,支持癌的发生、进展和转移。TAFs 还促成了免疫抑制性肿瘤微环境(TME),并阻碍 T 淋巴细胞杀伤肿瘤。本文讨论了 TAFs 在 TME 中的作用。具体来说,TAFs 为 T 淋巴细胞的浸润形成了屏障。TAFs 也作为 T 淋巴细胞的负调节剂。这些发现表明,靶向 TAFs 是改善癌症免疫治疗的一种有前途的策略。我们之前的研究表明,治疗性纳米颗粒有能力分布到 TAFs 中,并耗竭或失活 TAFs。本文将在开发针对癌症的特异性和有效性免疫疗法的背景下讨论这一方法。