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诱导性三级淋巴结构:转化新型免疫疗法的前景与挑战。

Inducible Tertiary Lymphoid Structures: Promise and Challenges for Translating a New Class of Immunotherapy.

机构信息

Department of Surgery, Institute of Gastroenterology, Tokyo Women's Medical University, Tokyo, Japan.

Immunology Program, Moffitt Cancer Center, Tampa, FL, United States.

出版信息

Front Immunol. 2021 May 14;12:675538. doi: 10.3389/fimmu.2021.675538. eCollection 2021.

Abstract

Tertiary lymphoid structures (TLS) are ectopically formed aggregates of organized lymphocytes and antigen-presenting cells that occur in solid tissues as part of a chronic inflammation response. Sharing structural and functional characteristics with conventional secondary lymphoid organs (SLO) including discrete T cell zones, B cell zones, marginal zones with antigen presenting cells, reticular stromal networks, and high endothelial venues (HEV), TLS are prominent centers of antigen presentation and adaptive immune activation within the periphery. TLS share many signaling axes and leukocyte recruitment schemes with SLO regarding their formation and function. In cancer, their presence confers positive prognostic value across a wide spectrum of indications, spurring interest in their artificial induction as either a new form of immunotherapy, or as a means to augment other cell or immunotherapies. Here, we review approaches for inducible (iTLS) that utilize chemokines, inflammatory factors, or cellular analogues vital to TLS formation and that often mirror conventional SLO organogenesis. This review also addresses biomaterials that have been or might be suitable for iTLS, and discusses remaining challenges facing iTLS manufacturing approaches for clinical translation.

摘要

三级淋巴结构 (TLS) 是异位形成的组织淋巴细胞和抗原呈递细胞的聚集物,作为慢性炎症反应的一部分发生在实体组织中。TLS 具有与传统次级淋巴器官 (SLO) 相似的结构和功能特征,包括离散的 T 细胞区、B 细胞区、具有抗原呈递细胞的边缘区、网状基质网络和高内皮静脉 (HEV),是外周组织中抗原呈递和适应性免疫激活的重要中心。TLS 在其形成和功能方面与 SLO 共享许多信号轴和白细胞募集方案。在癌症中,它们的存在在广泛的适应证中赋予了积极的预后价值,这激发了人们对其人工诱导的兴趣,无论是作为一种新的免疫疗法形式,还是作为增强其他细胞或免疫疗法的手段。在这里,我们综述了诱导性 (iTLS) 的方法,这些方法利用了对 TLS 形成至关重要的趋化因子、炎症因子或细胞类似物,这些方法通常与传统的 SLO 器官发生相吻合。这篇综述还讨论了已经或可能适合 iTLS 的生物材料,并讨论了 iTLS 制造方法在临床转化方面面临的剩余挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e70/8160316/dc0621ad8471/fimmu-12-675538-g001.jpg

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