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Immunotherapy Deriving from CAR-T Cell Treatment in Autoimmune Diseases

Chimeric antigen receptor T (CAR-T) cells are T cells engineered to express specific synthetic antigen receptors that can recognize antigens expressed by tumor cells, which after the binding of these antigens to the receptors are eliminated, and have been adopted to treat several kinds of malignanci...

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Autores principales: Chen, Yuehong, Sun, Jianhong, Liu, Huan, Yin, Geng, Xie, Qibing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012264/
https://www.ncbi.nlm.nih.gov/pubmed/32083141
http://dx.doi.org/10.1155/2019/5727516
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author Chen, Yuehong
Sun, Jianhong
Liu, Huan
Yin, Geng
Xie, Qibing
author_facet Chen, Yuehong
Sun, Jianhong
Liu, Huan
Yin, Geng
Xie, Qibing
author_sort Chen, Yuehong
collection PubMed
description Chimeric antigen receptor T (CAR-T) cells are T cells engineered to express specific synthetic antigen receptors that can recognize antigens expressed by tumor cells, which after the binding of these antigens to the receptors are eliminated, and have been adopted to treat several kinds of malignancies. Autoimmune diseases (AIDs), a class of chronic disease conditions, can be broadly separated into autoantibody-mediated and T cell-mediated diseases. Treatments for AIDs are focused on restoring immune tolerance. However, current treatments have little effect on immune tolerance inverse; even the molecular target biologics like anti-TNFα inhibitors can only mildly restore immune balance. By using the idea of CAR-T cell treatment in tumors, CAR-T cell-derived immunotherapies, chimeric autoantibody receptor T (CAAR-T) cells, and CAR regulatory T (CAR-T) cells bring new hope of treatment choice for AIDs.
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spelling pubmed-70122642020-02-20 Immunotherapy Deriving from CAR-T Cell Treatment in Autoimmune Diseases Chen, Yuehong Sun, Jianhong Liu, Huan Yin, Geng Xie, Qibing J Immunol Res Review Article Chimeric antigen receptor T (CAR-T) cells are T cells engineered to express specific synthetic antigen receptors that can recognize antigens expressed by tumor cells, which after the binding of these antigens to the receptors are eliminated, and have been adopted to treat several kinds of malignancies. Autoimmune diseases (AIDs), a class of chronic disease conditions, can be broadly separated into autoantibody-mediated and T cell-mediated diseases. Treatments for AIDs are focused on restoring immune tolerance. However, current treatments have little effect on immune tolerance inverse; even the molecular target biologics like anti-TNFα inhibitors can only mildly restore immune balance. By using the idea of CAR-T cell treatment in tumors, CAR-T cell-derived immunotherapies, chimeric autoantibody receptor T (CAAR-T) cells, and CAR regulatory T (CAR-T) cells bring new hope of treatment choice for AIDs. Hindawi 2019-12-31 /pmc/articles/PMC7012264/ /pubmed/32083141 http://dx.doi.org/10.1155/2019/5727516 Text en Copyright © 2019 Yuehong Chen et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Chen, Yuehong
Sun, Jianhong
Liu, Huan
Yin, Geng
Xie, Qibing
Immunotherapy Deriving from CAR-T Cell Treatment in Autoimmune Diseases
title Immunotherapy Deriving from CAR-T Cell Treatment in Autoimmune Diseases
title_full Immunotherapy Deriving from CAR-T Cell Treatment in Autoimmune Diseases
title_fullStr Immunotherapy Deriving from CAR-T Cell Treatment in Autoimmune Diseases
title_full_unstemmed Immunotherapy Deriving from CAR-T Cell Treatment in Autoimmune Diseases
title_short Immunotherapy Deriving from CAR-T Cell Treatment in Autoimmune Diseases
title_sort immunotherapy deriving from car-t cell treatment in autoimmune diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012264/
https://www.ncbi.nlm.nih.gov/pubmed/32083141
http://dx.doi.org/10.1155/2019/5727516
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