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细胞治疗诱导免疫耐受的前景。

Prospects of the Use of Cell Therapy to Induce Immune Tolerance.

机构信息

Central Laboratory of Hematology and Oncology, First Affiliated Hospital, Harbin Medical University, Harbin, China.

College of Life Science, Northeast Agricultural University, Harbin, China.

出版信息

Front Immunol. 2020 May 12;11:792. doi: 10.3389/fimmu.2020.00792. eCollection 2020.

DOI:10.3389/fimmu.2020.00792
PMID:32477335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7235417/
Abstract

Conditions in which abnormal or excessive immune responses exist, such as autoimmune diseases (ADs), graft-versus-host disease, transplant rejection, and hypersensitivity reactions, are serious hazards to human health and well-being. The traditional immunosuppressive drugs used to treat these conditions can lead to decreased immune function, a higher risk of infection, and increased tumor susceptibility. As an alternative therapeutic approach, cell therapy, in which generally intact and living cells are injected, grafted, or implanted into a patient, has the potential to overcome the limitations of traditional drug treatment and to alleviate the symptoms of many refractory diseases. Cell therapy could be a powerful approach to induce immune tolerance and restore immune homeostasis with a deeper understanding of immune tolerance mechanisms and the development of new techniques. The purpose of this review is to describe the current panoramic scope of cell therapy for immune-mediated disorders, discuss the advantages and disadvantages of different types of cell therapy, and explore novel directions and future prospects for these tolerogenic therapies.

摘要

在存在异常或过度免疫反应的情况下,如自身免疫性疾病 (AD)、移植物抗宿主病、移植排斥和超敏反应,这些都是对人类健康和福祉的严重危害。用于治疗这些疾病的传统免疫抑制剂会导致免疫功能下降、感染风险增加和肿瘤易感性增加。作为一种替代治疗方法,细胞疗法通常将完整和存活的细胞注入、移植或植入患者体内,具有克服传统药物治疗局限性和缓解许多难治性疾病症状的潜力。随着对免疫耐受机制的深入了解和新技术的发展,细胞疗法可能成为诱导免疫耐受和恢复免疫平衡的有力方法。本文旨在描述细胞疗法治疗免疫介导性疾病的当前全景范围,讨论不同类型细胞疗法的优缺点,并探索这些耐受疗法的新方向和未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/53a5dc2fe274/fimmu-11-00792-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/592b268c3976/fimmu-11-00792-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/2f55909be730/fimmu-11-00792-g0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/621d99b541cc/fimmu-11-00792-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/f1cda49852c1/fimmu-11-00792-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/53a5dc2fe274/fimmu-11-00792-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/592b268c3976/fimmu-11-00792-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/2f55909be730/fimmu-11-00792-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/82aac5975719/fimmu-11-00792-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/621d99b541cc/fimmu-11-00792-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/f1cda49852c1/fimmu-11-00792-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec46/7235417/53a5dc2fe274/fimmu-11-00792-g0006.jpg

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