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抗降解植入生物材料建立了一个免疫抑制微环境,通过招募髓系细胞诱导T细胞耗竭。

Degradation-resistant implanted biomaterials establish an immunosuppressive microenvironment that induces T cell exhaustion by recruiting myeloid cells.

作者信息

Fan Qin, Dai Huaxing, Bai Jinyu, Xu Jialu, Ma Qingle, Fei Ziying, Zhou Xiaozhong, Leong Kam W, Wang Chao

机构信息

Institute of Functional Nano & Soft Materials, Jiangsu Key Laboratory for Carbon-based Functional Materials and Devices, Soochow University, Suzhou 215123, China.

Department of Orthopedics, The Second Affiliated Hospital of Soochow University, Suzhou 215004, China.

出版信息

Fundam Res. 2021 Nov 25;2(4):648-658. doi: 10.1016/j.fmre.2021.10.007. eCollection 2022 Jul.

DOI:10.1016/j.fmre.2021.10.007
PMID:38933993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11197691/
Abstract

Implanted biomaterials have transformed healthcare and the treatment of injury and disease, but their influence on the local immune landscape remains unclear. Here we discovered that degradation-resistant titanium-based implants establish an immunosuppressive microenvironment by recruiting myeloid cells, including monocytes, macrophages, neutrophils, and myeloid-lineage dendritic cells. Unlike normal tissues, the tissues nearby implants exhibit an chronic inflamed and immunosuppressive status characterised by myeloid-rich, T cell-exhaustion gene signature by single-cell RNA sequencing. Vitamin C treatment provides an effective strategy to rescue the immunosuppressive microenvironment, which can be used as a regular supplement to reduce the risk of malignant cell survival around the implants.

摘要

植入式生物材料已经改变了医疗保健以及损伤和疾病的治疗方式,但其对局部免疫环境的影响仍不清楚。在这里,我们发现抗降解钛基植入物通过招募髓系细胞(包括单核细胞、巨噬细胞、中性粒细胞和髓系谱系树突状细胞)建立了一个免疫抑制微环境。与正常组织不同,植入物附近的组织表现出慢性炎症和免疫抑制状态,通过单细胞RNA测序显示其具有富含髓系细胞、T细胞耗竭的基因特征。维生素C治疗提供了一种有效的策略来挽救免疫抑制微环境,它可以作为一种常规补充剂来降低植入物周围恶性细胞存活的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/a3e2620673d7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/3dc36ebd7eaa/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/80b5de1c1c94/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/df0f11e4c75a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/77aff7983449/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/53a6fd71a8f0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/a3e2620673d7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/3dc36ebd7eaa/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/80b5de1c1c94/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/df0f11e4c75a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/77aff7983449/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/53a6fd71a8f0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ae/11197691/a3e2620673d7/gr5.jpg

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