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Treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens
Surgical brain injury (SBI) defines complications induced by intracranial surgery, such as cerebral edema and other secondary injuries. In our study, intrathymic and hepatic portal vein injection of allogeneic myelin basic protein (MBP) or autogeneic brain cell suspensions were administered to a sta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995514/ https://www.ncbi.nlm.nih.gov/pubmed/27554621 http://dx.doi.org/10.1038/srep32030 |
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author | Yang, Weijian Liu, Yong Liu, Baolong Tan, Huajun Lu, Hao Wang, Hong Yan, Hua |
author_facet | Yang, Weijian Liu, Yong Liu, Baolong Tan, Huajun Lu, Hao Wang, Hong Yan, Hua |
author_sort | Yang, Weijian |
collection | PubMed |
description | Surgical brain injury (SBI) defines complications induced by intracranial surgery, such as cerebral edema and other secondary injuries. In our study, intrathymic and hepatic portal vein injection of allogeneic myelin basic protein (MBP) or autogeneic brain cell suspensions were administered to a standard SBI model. Serum pro-inflammatory IL-2, anti-inflammatory IL-4 concentrations and the CD4(+)T/CD8(+)T ratio were measured at 1, 3, 7, 14 and 21 d after surgery to verify the establishment of immune tolerance. Furthermore, we confirmed neuroprotective effects by evaluating neurological scores at 1, 3, 7, 14 and 21 d after SBI. Anti-Fas ligand (FasL) immunohistochemistry and TUNEL assays of brain sections were tested at 21 d after surgery. Intrathymic injections of MBP or autogeneic brain cell suspensions functioned by both suppressing secondary inflammatory reactions and improving prognoses, whereas hepatic portal vein injections of autogeneic brain cell suspensions exerted a better effect than MBP. Intrathymic and hepatic portal vein injections of MBP had equal effects on reducing secondary inflammation and improving prognoses. Otherwise, hepatic portal vein injections of autogeneic brain cell suspensions had better outcomes than intrathymic injections of autogeneic brain cell suspensions. Moreover, the benefit of injecting antigens into the thymus was outweighed by hepatic portal vein injections. |
format | Online Article Text |
id | pubmed-4995514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49955142016-08-30 Treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens Yang, Weijian Liu, Yong Liu, Baolong Tan, Huajun Lu, Hao Wang, Hong Yan, Hua Sci Rep Article Surgical brain injury (SBI) defines complications induced by intracranial surgery, such as cerebral edema and other secondary injuries. In our study, intrathymic and hepatic portal vein injection of allogeneic myelin basic protein (MBP) or autogeneic brain cell suspensions were administered to a standard SBI model. Serum pro-inflammatory IL-2, anti-inflammatory IL-4 concentrations and the CD4(+)T/CD8(+)T ratio were measured at 1, 3, 7, 14 and 21 d after surgery to verify the establishment of immune tolerance. Furthermore, we confirmed neuroprotective effects by evaluating neurological scores at 1, 3, 7, 14 and 21 d after SBI. Anti-Fas ligand (FasL) immunohistochemistry and TUNEL assays of brain sections were tested at 21 d after surgery. Intrathymic injections of MBP or autogeneic brain cell suspensions functioned by both suppressing secondary inflammatory reactions and improving prognoses, whereas hepatic portal vein injections of autogeneic brain cell suspensions exerted a better effect than MBP. Intrathymic and hepatic portal vein injections of MBP had equal effects on reducing secondary inflammation and improving prognoses. Otherwise, hepatic portal vein injections of autogeneic brain cell suspensions had better outcomes than intrathymic injections of autogeneic brain cell suspensions. Moreover, the benefit of injecting antigens into the thymus was outweighed by hepatic portal vein injections. Nature Publishing Group 2016-08-24 /pmc/articles/PMC4995514/ /pubmed/27554621 http://dx.doi.org/10.1038/srep32030 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yang, Weijian Liu, Yong Liu, Baolong Tan, Huajun Lu, Hao Wang, Hong Yan, Hua Treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens |
title | Treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens |
title_full | Treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens |
title_fullStr | Treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens |
title_full_unstemmed | Treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens |
title_short | Treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens |
title_sort | treatment of surgical brain injury by immune tolerance induced by intrathymic and hepatic portal vein injection of brain antigens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995514/ https://www.ncbi.nlm.nih.gov/pubmed/27554621 http://dx.doi.org/10.1038/srep32030 |
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