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Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease
Activation of T lymphocytes is the initiating factor of the occurrence of acute graft-versus-host disease (aGVHD), and cytotoxic T lymphocyte antigen-4 (CTLA-4) is the inhibitory receptor for activating T cells. T cell immune response cDNA 7 (TIRC7) is considered an upstream regulator of CTLA-4; how...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577082/ https://www.ncbi.nlm.nih.gov/pubmed/33101494 http://dx.doi.org/10.3892/ol.2020.12163 |
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author | Zhu, Feng Xu, Yanqiu Fan, Xiaohui Zhang, Fan Wang, Dong Qiao, Jianlin Zhu, Shengyun Zhao, Kai Pan, Bin Chen, Chong Zeng, Lingyu Li, Zhenyu Xu, Kailin |
author_facet | Zhu, Feng Xu, Yanqiu Fan, Xiaohui Zhang, Fan Wang, Dong Qiao, Jianlin Zhu, Shengyun Zhao, Kai Pan, Bin Chen, Chong Zeng, Lingyu Li, Zhenyu Xu, Kailin |
author_sort | Zhu, Feng |
collection | PubMed |
description | Activation of T lymphocytes is the initiating factor of the occurrence of acute graft-versus-host disease (aGVHD), and cytotoxic T lymphocyte antigen-4 (CTLA-4) is the inhibitory receptor for activating T cells. T cell immune response cDNA 7 (TIRC7) is considered an upstream regulator of CTLA-4; however, little is understood regarding the effects of TIRC7 on the regulation of CTLA-4 in aGVHD. The purpose of the present study was to evaluate the regulatory effects of TIRC7 on aGVHD, mainly in the pathology. Recipient mice were exposed to a preconditioning dose of 7.5 Gy irradiation on the day of the transplantation and were divided into the following groups: Blank control group, bone marrow transplantation control group, total body irradiation group, mild-moderate aGVHD group and severe aGVHD group. According to the different administration of CTLA-4 and TIRC7 monoclonal antibodies, the mild-moderate and severe aGVHD groups were randomly divided into the hematopoietic stem cell transplantation (HSCT) and HSCT + CTLA-4/TIRC7 groups. Recipient mice were sacrificed at different time points post-HSCT for histopathological analysis by hematoxylin and eosin staining. Compared with the control and other experimental groups, the mice in the combined CTLA-4 and TIRC7 group exhibited ameliorated pathological injury, and lower pathology scores of the liver, lung and intestine. These data revealed that intraperitoneal injection of anti-TIRC7 and/or anti-CTLA-4 monoclonal antibody into mice could effectively alleviate the severity of aGVHD. |
format | Online Article Text |
id | pubmed-7577082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-75770822020-10-22 Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease Zhu, Feng Xu, Yanqiu Fan, Xiaohui Zhang, Fan Wang, Dong Qiao, Jianlin Zhu, Shengyun Zhao, Kai Pan, Bin Chen, Chong Zeng, Lingyu Li, Zhenyu Xu, Kailin Oncol Lett Articles Activation of T lymphocytes is the initiating factor of the occurrence of acute graft-versus-host disease (aGVHD), and cytotoxic T lymphocyte antigen-4 (CTLA-4) is the inhibitory receptor for activating T cells. T cell immune response cDNA 7 (TIRC7) is considered an upstream regulator of CTLA-4; however, little is understood regarding the effects of TIRC7 on the regulation of CTLA-4 in aGVHD. The purpose of the present study was to evaluate the regulatory effects of TIRC7 on aGVHD, mainly in the pathology. Recipient mice were exposed to a preconditioning dose of 7.5 Gy irradiation on the day of the transplantation and were divided into the following groups: Blank control group, bone marrow transplantation control group, total body irradiation group, mild-moderate aGVHD group and severe aGVHD group. According to the different administration of CTLA-4 and TIRC7 monoclonal antibodies, the mild-moderate and severe aGVHD groups were randomly divided into the hematopoietic stem cell transplantation (HSCT) and HSCT + CTLA-4/TIRC7 groups. Recipient mice were sacrificed at different time points post-HSCT for histopathological analysis by hematoxylin and eosin staining. Compared with the control and other experimental groups, the mice in the combined CTLA-4 and TIRC7 group exhibited ameliorated pathological injury, and lower pathology scores of the liver, lung and intestine. These data revealed that intraperitoneal injection of anti-TIRC7 and/or anti-CTLA-4 monoclonal antibody into mice could effectively alleviate the severity of aGVHD. D.A. Spandidos 2020-12 2020-09-28 /pmc/articles/PMC7577082/ /pubmed/33101494 http://dx.doi.org/10.3892/ol.2020.12163 Text en Copyright: © Zhu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zhu, Feng Xu, Yanqiu Fan, Xiaohui Zhang, Fan Wang, Dong Qiao, Jianlin Zhu, Shengyun Zhao, Kai Pan, Bin Chen, Chong Zeng, Lingyu Li, Zhenyu Xu, Kailin Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease |
title | Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease |
title_full | Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease |
title_fullStr | Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease |
title_full_unstemmed | Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease |
title_short | Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease |
title_sort | role of t cell immune response cdna 7 on the pathology of acute graft-versus-host disease |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577082/ https://www.ncbi.nlm.nih.gov/pubmed/33101494 http://dx.doi.org/10.3892/ol.2020.12163 |
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