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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-...

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Autores principales: Beers, David R., Zhao, Weihua, Thonhoff, Jason R., Faridar, Alireza, Thome, Aaron D., Wen, Shixiang, Wang, Jinghong, Appel, Stanley H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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.
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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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