Department of Pharmacology and Experimental Therapeutics, Boston University, Boston, MA, United States.
Department of Biomedical Engineering, University of Texas Austin, Austin, TX, United States.
Front Immunol. 2020 Oct 21;11:521110. doi: 10.3389/fimmu.2020.521110. eCollection 2020.
Tumor immunity is a rapidly evolving area of research consisting of many possible permutations of immune cell tumor interactions that are dependent upon cell type, tumor type, and stage in tumor progression. At the same time, the majority of cancer immunotherapies have been focused on modulating the T cell-mediated antitumor immune response and have largely ignored the potential utility that B cells possess with respect to tumor immunity. Therefore, this motivated an exploration into the role that B cells and their accompanying chemokine, CXCL13, play in tumor immunity across multiple tumor types. Both B cells and CXCL13 possess dualistic impacts on tumor progression and tumor immunity which is furthered detail in this review. Specifically, various B cells subtypes are able to suppress or enhance several important immunological functions. Paradoxically, CXCL13 has been shown to drive several pro-growth and invasive signaling pathways across multiple tumor types, while also, correlating with improved survival and immune cell tumor localization in other tumor types. Potential tools for better elucidating the mechanisms by which B cells and CXCL13 impact the antitumor immune response are also discussed. In addition, multiples strategies are proposed for modulating the B cell-CXCL13 axis for cancer immunotherapies.
肿瘤免疫是一个快速发展的研究领域,其中包含许多可能的免疫细胞与肿瘤相互作用的排列组合,这些组合取决于细胞类型、肿瘤类型和肿瘤进展阶段。与此同时,大多数癌症免疫疗法都集中在调节 T 细胞介导的抗肿瘤免疫反应上,而在很大程度上忽略了 B 细胞在肿瘤免疫方面可能具有的潜在效用。因此,这促使人们探索 B 细胞及其伴随的趋化因子 CXCL13 在多种肿瘤类型中的肿瘤免疫中的作用。B 细胞和 CXCL13 对肿瘤进展和肿瘤免疫都具有双重影响,这在本综述中有详细描述。具体来说,各种 B 细胞亚型能够抑制或增强几种重要的免疫功能。矛盾的是,CXCL13 已被证明在多种肿瘤类型中驱动几种促生长和侵袭信号通路,同时与其他肿瘤类型中改善的生存和免疫细胞肿瘤定位相关。还讨论了用于更好地阐明 B 细胞和 CXCL13 影响抗肿瘤免疫反应的机制的潜在工具。此外,还提出了多种调节 B 细胞-CXCL13 轴的策略用于癌症免疫疗法。