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Serum programmed cell death proteins in amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a multifactorial, multisystem pro-inflammatory neuromuscular disorder. Activation of programmed cell death-1 (PD-1), and its ligands, programmed cell death-ligand 1 and 2 (PD-L1/L2), leads to immune suppression. Serum soluble forms of these proteins, sPD-1/sPD-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474632/ https://www.ncbi.nlm.nih.gov/pubmed/34589734 http://dx.doi.org/10.1016/j.bbih.2021.100209 |
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author | Beers, David R. Zhao, Weihua Thonhoff, Jason R. Faridar, Alireza Thome, Aaron D. Wen, Shixiang Wang, Jinghong Appel, Stanley H. |
author_facet | Beers, David R. Zhao, Weihua Thonhoff, Jason R. Faridar, Alireza Thome, Aaron D. Wen, Shixiang Wang, Jinghong Appel, Stanley H. |
author_sort | Beers, David R. |
collection | PubMed |
description | Amyotrophic lateral sclerosis (ALS) is a multifactorial, multisystem pro-inflammatory neuromuscular disorder. Activation of programmed cell death-1 (PD-1), and its ligands, programmed cell death-ligand 1 and 2 (PD-L1/L2), leads to immune suppression. Serum soluble forms of these proteins, sPD-1/sPD-L1/sPD-L2, inhibit this suppression and promote pro-inflammatory responses. The purpose of this study was to determine if sPD-1, sPD-L1, and sPD-L2 were increased in sera of patients with ALS. sPD-1 and sPD-L2 were elevated in sera of patients and accurately reflected patients’ disease burdens. Increased sera levels of programmed cell death proteins reinforce the concept that peripheral pro-inflammatory responses contribute to systemic inflammation in patients with ALS. |
format | Online Article Text |
id | pubmed-8474632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-84746322021-09-28 Serum programmed cell death proteins in amyotrophic lateral sclerosis Beers, David R. Zhao, Weihua Thonhoff, Jason R. Faridar, Alireza Thome, Aaron D. Wen, Shixiang Wang, Jinghong Appel, Stanley H. Brain Behav Immun Health Short Communication Amyotrophic lateral sclerosis (ALS) is a multifactorial, multisystem pro-inflammatory neuromuscular disorder. Activation of programmed cell death-1 (PD-1), and its ligands, programmed cell death-ligand 1 and 2 (PD-L1/L2), leads to immune suppression. Serum soluble forms of these proteins, sPD-1/sPD-L1/sPD-L2, inhibit this suppression and promote pro-inflammatory responses. The purpose of this study was to determine if sPD-1, sPD-L1, and sPD-L2 were increased in sera of patients with ALS. sPD-1 and sPD-L2 were elevated in sera of patients and accurately reflected patients’ disease burdens. Increased sera levels of programmed cell death proteins reinforce the concept that peripheral pro-inflammatory responses contribute to systemic inflammation in patients with ALS. Elsevier 2021-01-26 /pmc/articles/PMC8474632/ /pubmed/34589734 http://dx.doi.org/10.1016/j.bbih.2021.100209 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Short Communication Beers, David R. Zhao, Weihua Thonhoff, Jason R. Faridar, Alireza Thome, Aaron D. Wen, Shixiang Wang, Jinghong Appel, Stanley H. Serum programmed cell death proteins in amyotrophic lateral sclerosis |
title | Serum programmed cell death proteins in amyotrophic lateral sclerosis |
title_full | Serum programmed cell death proteins in amyotrophic lateral sclerosis |
title_fullStr | Serum programmed cell death proteins in amyotrophic lateral sclerosis |
title_full_unstemmed | Serum programmed cell death proteins in amyotrophic lateral sclerosis |
title_short | Serum programmed cell death proteins in amyotrophic lateral sclerosis |
title_sort | serum programmed cell death proteins in amyotrophic lateral sclerosis |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474632/ https://www.ncbi.nlm.nih.gov/pubmed/34589734 http://dx.doi.org/10.1016/j.bbih.2021.100209 |
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