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Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis
Sphingosine-1-phosphate receptor subtype 1 (S1P(1)) is essential for lymphocyte egress from lymphoid organs into systemic circulation and provides a well-defined drug target for autoimmune disorders. IMMH001, also called SYL930, is a specific S1P(1)/S1P(4)/S1P(5) modulator. Here, we investigated the...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761374/ https://www.ncbi.nlm.nih.gov/pubmed/31607926 http://dx.doi.org/10.3389/fphar.2019.01085 |
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author | Jin, Jing Ji, Ming Fu, Rong Wang, Mingjin Xue, Nina Xiao, Qiong Hu, Jingpin Wang, Xiaojian Lai, Fangfang Yin, Dali Chen, Xiaoguang |
author_facet | Jin, Jing Ji, Ming Fu, Rong Wang, Mingjin Xue, Nina Xiao, Qiong Hu, Jingpin Wang, Xiaojian Lai, Fangfang Yin, Dali Chen, Xiaoguang |
author_sort | Jin, Jing |
collection | PubMed |
description | Sphingosine-1-phosphate receptor subtype 1 (S1P(1)) is essential for lymphocyte egress from lymphoid organs into systemic circulation and provides a well-defined drug target for autoimmune disorders. IMMH001, also called SYL930, is a specific S1P(1)/S1P(4)/S1P(5) modulator. Here, we investigated the potential therapeutic effect of IMMH001 on rheumatoid arthritis (RA). IMMH001 rendered periphery blood lymphocytes insensitive to the egress signal from secondary lymphoid organs. Importantly, in both rat adjuvant-induced arthritis and collagen-induced arthritis models, IMMH001 treatment significantly inhibited the progression of RA and RA-associated histological changes in the joints of Sprague-Dawley rats, including hind paw swelling and arthritic index, and thus reduced the pathological score. Furthermore, IMMH001 markedly decreased proinflammatory cytokine and chemokine release from the damaged joints. These data demonstrated that IMMH001 is a promising drug candidate for RA treatment. |
format | Online Article Text |
id | pubmed-6761374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67613742019-10-13 Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis Jin, Jing Ji, Ming Fu, Rong Wang, Mingjin Xue, Nina Xiao, Qiong Hu, Jingpin Wang, Xiaojian Lai, Fangfang Yin, Dali Chen, Xiaoguang Front Pharmacol Pharmacology Sphingosine-1-phosphate receptor subtype 1 (S1P(1)) is essential for lymphocyte egress from lymphoid organs into systemic circulation and provides a well-defined drug target for autoimmune disorders. IMMH001, also called SYL930, is a specific S1P(1)/S1P(4)/S1P(5) modulator. Here, we investigated the potential therapeutic effect of IMMH001 on rheumatoid arthritis (RA). IMMH001 rendered periphery blood lymphocytes insensitive to the egress signal from secondary lymphoid organs. Importantly, in both rat adjuvant-induced arthritis and collagen-induced arthritis models, IMMH001 treatment significantly inhibited the progression of RA and RA-associated histological changes in the joints of Sprague-Dawley rats, including hind paw swelling and arthritic index, and thus reduced the pathological score. Furthermore, IMMH001 markedly decreased proinflammatory cytokine and chemokine release from the damaged joints. These data demonstrated that IMMH001 is a promising drug candidate for RA treatment. Frontiers Media S.A. 2019-09-19 /pmc/articles/PMC6761374/ /pubmed/31607926 http://dx.doi.org/10.3389/fphar.2019.01085 Text en Copyright © 2019 Jin, Ji, Fu, Wang, Xue, Xiao, Hu, Wang, Lai, Yin and Chen http://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 | Pharmacology Jin, Jing Ji, Ming Fu, Rong Wang, Mingjin Xue, Nina Xiao, Qiong Hu, Jingpin Wang, Xiaojian Lai, Fangfang Yin, Dali Chen, Xiaoguang Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis |
title | Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis |
title_full | Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis |
title_fullStr | Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis |
title_full_unstemmed | Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis |
title_short | Sphingosine-1-Phosphate Receptor Subtype 1 (S1P1) Modulator IMMH001 Regulates Adjuvant- and Collagen-Induced Arthritis |
title_sort | sphingosine-1-phosphate receptor subtype 1 (s1p1) modulator immh001 regulates adjuvant- and collagen-induced arthritis |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761374/ https://www.ncbi.nlm.nih.gov/pubmed/31607926 http://dx.doi.org/10.3389/fphar.2019.01085 |
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