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肿瘤微环境中调节性 T 细胞的调控。

Regulation of regulatory T cells in cancer.

机构信息

CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.

Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.

出版信息

Immunology. 2019 Jul;157(3):219-231. doi: 10.1111/imm.13064. Epub 2019 May 22.

Abstract

The inflammatory response to transformed cells forms the cornerstone of natural or therapeutically induced protective immunity to cancer. Regulatory T (Treg) cells are known for their critical role in suppressing inflammation, and therefore can antagonize effective anti-cancer immune responses. As such, Treg cells can play detrimental roles in tumour progression and in the response to both conventional and immune-based cancer therapies. Recent advances in our understanding of Treg cells reveal complex niche-specific regulatory programmes and functions, which are likely to extrapolate to cancer. The regulation of Treg cells is reliant on upstream cues from haematopoietic and non-immune cells, which dictates their genetic, epigenetic and downstream functional programmes. In this review we will discuss how Treg cells are themselves regulated in normal and transformed tissues, and the implications of this cross talk on tumour growth.

摘要

对转化细胞的炎症反应构成了天然或治疗性诱导的抗肿瘤保护性免疫的基石。调节性 T(Treg)细胞在抑制炎症方面的关键作用是众所周知的,因此可以拮抗有效的抗肿瘤免疫反应。因此,Treg 细胞在肿瘤进展以及对常规和基于免疫的癌症治疗的反应中可能发挥有害作用。我们对 Treg 细胞的理解的最新进展揭示了复杂的特定生态位的调节程序和功能,这些可能外推到癌症。Treg 细胞的调节依赖于造血细胞和非免疫细胞的上游线索,这些线索决定了它们的遗传、表观遗传和下游功能程序。在这篇综述中,我们将讨论 Treg 细胞在正常和转化组织中是如何被自身调节的,以及这种串扰对肿瘤生长的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e2/6587396/02b78d22f114/IMM-157-219-g001.jpg

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