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Anti-Integrin Therapy for Multiple Sclerosis

Integrins are the foremost family of cell adhesion molecules that regulate immune cell trafficking in health and diseases. Integrin alpha4 mediates organ-specific migration of immune cells to the inflamed brain, thereby playing the critical role in the pathogenesis of multiple sclerosis. Anti-alpha4...

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Detalles Bibliográficos
Autores principales: Kawamoto, Eiji, Nakahashi, Susumu, Okamoto, Takayuki, Imai, Hiroshi, Shimaoka, Motomu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533681/
https://www.ncbi.nlm.nih.gov/pubmed/23346387
http://dx.doi.org/10.1155/2012/357101
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author Kawamoto, Eiji
Nakahashi, Susumu
Okamoto, Takayuki
Imai, Hiroshi
Shimaoka, Motomu
author_facet Kawamoto, Eiji
Nakahashi, Susumu
Okamoto, Takayuki
Imai, Hiroshi
Shimaoka, Motomu
author_sort Kawamoto, Eiji
collection PubMed
description Integrins are the foremost family of cell adhesion molecules that regulate immune cell trafficking in health and diseases. Integrin alpha4 mediates organ-specific migration of immune cells to the inflamed brain, thereby playing the critical role in the pathogenesis of multiple sclerosis. Anti-alpha4 integrin therapy aiming to block infiltration of autoreactive lymphocytes to the inflamed brain has been validated in several clinical trials for the treatment of multiple sclerosis. This paper provides readers with an overview of the molecular and structural bases of integrin activation as well as rationale for using anti-alpha4 integrin therapy for multiple sclerosis and then chronicles the rise and fall of this treatment strategy using natalizumab, a humanized anti-alpha4 integrin.
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spelling pubmed-35336812013-01-23 Anti-Integrin Therapy for Multiple Sclerosis Kawamoto, Eiji Nakahashi, Susumu Okamoto, Takayuki Imai, Hiroshi Shimaoka, Motomu Autoimmune Dis Review Article Integrins are the foremost family of cell adhesion molecules that regulate immune cell trafficking in health and diseases. Integrin alpha4 mediates organ-specific migration of immune cells to the inflamed brain, thereby playing the critical role in the pathogenesis of multiple sclerosis. Anti-alpha4 integrin therapy aiming to block infiltration of autoreactive lymphocytes to the inflamed brain has been validated in several clinical trials for the treatment of multiple sclerosis. This paper provides readers with an overview of the molecular and structural bases of integrin activation as well as rationale for using anti-alpha4 integrin therapy for multiple sclerosis and then chronicles the rise and fall of this treatment strategy using natalizumab, a humanized anti-alpha4 integrin. Hindawi Publishing Corporation 2012 2012-12-17 /pmc/articles/PMC3533681/ /pubmed/23346387 http://dx.doi.org/10.1155/2012/357101 Text en Copyright © 2012 Eiji Kawamoto et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kawamoto, Eiji
Nakahashi, Susumu
Okamoto, Takayuki
Imai, Hiroshi
Shimaoka, Motomu
Anti-Integrin Therapy for Multiple Sclerosis
title Anti-Integrin Therapy for Multiple Sclerosis
title_full Anti-Integrin Therapy for Multiple Sclerosis
title_fullStr Anti-Integrin Therapy for Multiple Sclerosis
title_full_unstemmed Anti-Integrin Therapy for Multiple Sclerosis
title_short Anti-Integrin Therapy for Multiple Sclerosis
title_sort anti-integrin therapy for multiple sclerosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533681/
https://www.ncbi.nlm.nih.gov/pubmed/23346387
http://dx.doi.org/10.1155/2012/357101
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