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Live Imaging of Immune Responses in Experimental Models of Multiple Sclerosis
Experimental autoimmune encephalomyelitis (EAE) is the most common animal model of multiple sclerosis (MS), a chronic inflammatory autoimmune disease of the central nervous system (CNS) characterized by multifocal perivascular infiltrates that predominantly comprise lymphocytes and macrophages. Duri...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116921/ https://www.ncbi.nlm.nih.gov/pubmed/27917173 http://dx.doi.org/10.3389/fimmu.2016.00506 |
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author | Rossi, Barbara Constantin, Gabriela |
author_facet | Rossi, Barbara Constantin, Gabriela |
author_sort | Rossi, Barbara |
collection | PubMed |
description | Experimental autoimmune encephalomyelitis (EAE) is the most common animal model of multiple sclerosis (MS), a chronic inflammatory autoimmune disease of the central nervous system (CNS) characterized by multifocal perivascular infiltrates that predominantly comprise lymphocytes and macrophages. During EAE, autoreactive T cells first become active in the secondary lymphoid organs upon contact with antigen-presenting cells (APCs), and then gain access to CNS parenchyma, through a compromised blood–brain barrier, subsequently inducing inflammation and demyelination. Two-photon laser scanning microscopy (TPLSM) is an ideal tool for intravital imaging because of its low phototoxicity, deep tissue penetration, and high resolution. In the last decade, TPLSM has been used to visualize the behavior of T cells and their contact with APCs in the lymph nodes (LNs) and target tissues in several models of autoimmune diseases. The leptomeninges and cerebrospinal fluid represent particularly important points for T cell entry into the CNS and reactivation following contact with local APCs during the preclinical phase of EAE. In this review, we highlight recent findings concerning the pathogenesis of EAE and MS, emphasizing the use of TPLSM to characterize T cell activation in the LNs and CNS, as well as the mechanisms of tolerance induction. Furthermore, we discuss how advanced imaging unveils disease mechanisms and helps to identify novel therapeutic strategies to treat CNS autoimmunity and inflammation. |
format | Online Article Text |
id | pubmed-5116921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51169212016-12-02 Live Imaging of Immune Responses in Experimental Models of Multiple Sclerosis Rossi, Barbara Constantin, Gabriela Front Immunol Immunology Experimental autoimmune encephalomyelitis (EAE) is the most common animal model of multiple sclerosis (MS), a chronic inflammatory autoimmune disease of the central nervous system (CNS) characterized by multifocal perivascular infiltrates that predominantly comprise lymphocytes and macrophages. During EAE, autoreactive T cells first become active in the secondary lymphoid organs upon contact with antigen-presenting cells (APCs), and then gain access to CNS parenchyma, through a compromised blood–brain barrier, subsequently inducing inflammation and demyelination. Two-photon laser scanning microscopy (TPLSM) is an ideal tool for intravital imaging because of its low phototoxicity, deep tissue penetration, and high resolution. In the last decade, TPLSM has been used to visualize the behavior of T cells and their contact with APCs in the lymph nodes (LNs) and target tissues in several models of autoimmune diseases. The leptomeninges and cerebrospinal fluid represent particularly important points for T cell entry into the CNS and reactivation following contact with local APCs during the preclinical phase of EAE. In this review, we highlight recent findings concerning the pathogenesis of EAE and MS, emphasizing the use of TPLSM to characterize T cell activation in the LNs and CNS, as well as the mechanisms of tolerance induction. Furthermore, we discuss how advanced imaging unveils disease mechanisms and helps to identify novel therapeutic strategies to treat CNS autoimmunity and inflammation. Frontiers Media S.A. 2016-11-21 /pmc/articles/PMC5116921/ /pubmed/27917173 http://dx.doi.org/10.3389/fimmu.2016.00506 Text en Copyright © 2016 Rossi and Constantin. 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) or licensor 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 | Immunology Rossi, Barbara Constantin, Gabriela Live Imaging of Immune Responses in Experimental Models of Multiple Sclerosis |
title | Live Imaging of Immune Responses in Experimental Models of Multiple Sclerosis |
title_full | Live Imaging of Immune Responses in Experimental Models of Multiple Sclerosis |
title_fullStr | Live Imaging of Immune Responses in Experimental Models of Multiple Sclerosis |
title_full_unstemmed | Live Imaging of Immune Responses in Experimental Models of Multiple Sclerosis |
title_short | Live Imaging of Immune Responses in Experimental Models of Multiple Sclerosis |
title_sort | live imaging of immune responses in experimental models of multiple sclerosis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116921/ https://www.ncbi.nlm.nih.gov/pubmed/27917173 http://dx.doi.org/10.3389/fimmu.2016.00506 |
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