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TIGIT as a Promising Therapeutic Target in Autoimmune Diseases
Co-inhibitory receptors (IRs) are molecules that protect host against autoimmune reactions and maintain peripheral self-tolerance, playing an essential role in maintaining immune homeostasis. In view of the substantial clinical progresses of negative immune checkpoint blockade in cancer treatment, t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203892/ https://www.ncbi.nlm.nih.gov/pubmed/35720417 http://dx.doi.org/10.3389/fimmu.2022.911919 |
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author | Yue, Chenran Gao, Sheng Li, Shuting Xing, Zhouhang Qian, Hengrong Hu, Ying Wang, Wenqian Hua, Chunyan |
author_facet | Yue, Chenran Gao, Sheng Li, Shuting Xing, Zhouhang Qian, Hengrong Hu, Ying Wang, Wenqian Hua, Chunyan |
author_sort | Yue, Chenran |
collection | PubMed |
description | Co-inhibitory receptors (IRs) are molecules that protect host against autoimmune reactions and maintain peripheral self-tolerance, playing an essential role in maintaining immune homeostasis. In view of the substantial clinical progresses of negative immune checkpoint blockade in cancer treatment, the role of IRs in autoimmune diseases is also obvious. Several advances highlighted the substantial impacts of T cell immunoglobulin and ITIM domain (TIGIT), a novel IR, in autoimmunity. Blockade of TIGIT pathway exacerbates multiple autoimmune diseases, whereas enhancement of TIGIT function has been shown to alleviate autoimmune settings in mice. These data suggested that TIGIT pathway can be manipulated to achieve durable tolerance to treat autoimmune disorders. In this review, we provide an overview of characteristics of TIGIT and its role in autoimmunity. We then discuss recent approaches and future directions to leverage our knowledge of TIGIT as therapeutic target in autoimmune diseases. |
format | Online Article Text |
id | pubmed-9203892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92038922022-06-18 TIGIT as a Promising Therapeutic Target in Autoimmune Diseases Yue, Chenran Gao, Sheng Li, Shuting Xing, Zhouhang Qian, Hengrong Hu, Ying Wang, Wenqian Hua, Chunyan Front Immunol Immunology Co-inhibitory receptors (IRs) are molecules that protect host against autoimmune reactions and maintain peripheral self-tolerance, playing an essential role in maintaining immune homeostasis. In view of the substantial clinical progresses of negative immune checkpoint blockade in cancer treatment, the role of IRs in autoimmune diseases is also obvious. Several advances highlighted the substantial impacts of T cell immunoglobulin and ITIM domain (TIGIT), a novel IR, in autoimmunity. Blockade of TIGIT pathway exacerbates multiple autoimmune diseases, whereas enhancement of TIGIT function has been shown to alleviate autoimmune settings in mice. These data suggested that TIGIT pathway can be manipulated to achieve durable tolerance to treat autoimmune disorders. In this review, we provide an overview of characteristics of TIGIT and its role in autoimmunity. We then discuss recent approaches and future directions to leverage our knowledge of TIGIT as therapeutic target in autoimmune diseases. Frontiers Media S.A. 2022-06-03 /pmc/articles/PMC9203892/ /pubmed/35720417 http://dx.doi.org/10.3389/fimmu.2022.911919 Text en Copyright © 2022 Yue, Gao, Li, Xing, Qian, Hu, Wang and Hua https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Yue, Chenran Gao, Sheng Li, Shuting Xing, Zhouhang Qian, Hengrong Hu, Ying Wang, Wenqian Hua, Chunyan TIGIT as a Promising Therapeutic Target in Autoimmune Diseases |
title | TIGIT as a Promising Therapeutic Target in Autoimmune Diseases |
title_full | TIGIT as a Promising Therapeutic Target in Autoimmune Diseases |
title_fullStr | TIGIT as a Promising Therapeutic Target in Autoimmune Diseases |
title_full_unstemmed | TIGIT as a Promising Therapeutic Target in Autoimmune Diseases |
title_short | TIGIT as a Promising Therapeutic Target in Autoimmune Diseases |
title_sort | tigit as a promising therapeutic target in autoimmune diseases |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203892/ https://www.ncbi.nlm.nih.gov/pubmed/35720417 http://dx.doi.org/10.3389/fimmu.2022.911919 |
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