Department of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan, 44919, South Korea.
Tissue Eng Regen Med. 2023 Jun;20(3):341-353. doi: 10.1007/s13770-023-00543-y. Epub 2023 Apr 20.
Considering the important role of the Peyer's patches (PPs) in gut immune balance, understanding of the detailed mechanisms that control and regulate the antigens in PPs can facilitate the development of immune therapeutic strategies against the gut inflammatory diseases.
In this review, we summarize the unique structure and function of intestinal PPs and current technologies to establish in vitro intestinal PP system focusing on M cell within the follicle-associated epithelium and IgA B cell models for studying mucosal immune networks. Furthermore, multidisciplinary approaches to establish more physiologically relevant PP model were proposed.
PPs are surrounded by follicle-associated epithelium containing microfold (M) cells, which serve as special gateways for luminal antigen transport across the gut epithelium. The transported antigens are processed by immune cells within PPs and then, antigen-specific mucosal immune response or mucosal tolerance is initiated, depending on the response of underlying mucosal immune cells. So far, there is no high fidelity (patho)physiological model of PPs; however, there have been several efforts to recapitulate the key steps of mucosal immunity in PPs such as antigen transport through M cells and mucosal IgA responses.
Current in vitro PP models are not sufficient to recapitulate how mucosal immune system works in PPs. Advanced three-dimensional cell culture technologies would enable to recapitulate the function of PPs, and bridge the gap between animal models and human.
鉴于派尔集合淋巴结(PPs)在肠道免疫平衡中的重要作用,了解控制和调节 PP 中抗原的详细机制有助于开发针对肠道炎症性疾病的免疫治疗策略。
在这篇综述中,我们总结了肠道 PPs 的独特结构和功能,以及当前建立体外肠道 PP 系统的技术,重点介绍了滤泡相关上皮内的 M 细胞和 IgA B 细胞模型,用于研究黏膜免疫网络。此外,还提出了多学科方法来建立更具生理相关性的 PP 模型。
PPs 被滤泡相关上皮包围,其中包含微褶皱(M)细胞,它们作为腔抗原穿过肠道上皮运输的特殊门户。运输的抗原由 PPs 内的免疫细胞处理,然后根据基础黏膜免疫细胞的反应,启动抗原特异性黏膜免疫反应或黏膜耐受。到目前为止,还没有高度保真的(病理)生理 PP 模型;然而,已经有一些努力试图重现 PPs 中黏膜免疫的关键步骤,如 M 细胞介导的抗原运输和黏膜 IgA 反应。
目前的体外 PP 模型不足以重现黏膜免疫系统在 PPs 中的工作方式。先进的三维细胞培养技术将能够重现 PPs 的功能,并弥合动物模型和人类之间的差距。