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Immunomodulatory Potential of Cannabidiol in Multiple Sclerosis: a Systematic Review
Multiple sclerosis (MS) is the most common chronic autoimmune disease of the central nervous system. Efficacy of treatments for MS is associated with risk of adverse effects, and effective and well-tolerated drugs remain a major unmet need. Cannabis (Cannabis sativa L., fam. Cannabaceae) and cannabi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829325/ https://www.ncbi.nlm.nih.gov/pubmed/33492630 http://dx.doi.org/10.1007/s11481-021-09982-7 |
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author | Furgiuele, Alessia Cosentino, Marco Ferrari, Marco Marino, Franca |
author_facet | Furgiuele, Alessia Cosentino, Marco Ferrari, Marco Marino, Franca |
author_sort | Furgiuele, Alessia |
collection | PubMed |
description | Multiple sclerosis (MS) is the most common chronic autoimmune disease of the central nervous system. Efficacy of treatments for MS is associated with risk of adverse effects, and effective and well-tolerated drugs remain a major unmet need. Cannabis (Cannabis sativa L., fam. Cannabaceae) and cannabinoids are popular among MS patients to treat spasticity and pain. Cannabinoids are endowed with remarkable immunomodulating properties, and in particular the non-psychotropic cannabinoid cannabidiol (CBD) is increasingly recognized as anti-inflammatory and immunosuppressive, nevertheless with excellent tolerability even at high doses. In this systematic review, we retrieved and critically evaluated available evidence regarding the immune and disease-modifying effects of CBD in experimental autoimmune encephalomyelitis (EAE) and in MS. Evidence in rodent models of EAE strongly supports CBD as effective, while clinical evidence is still limited and usually negative, due to paucity of studies and possibly to the use of suboptimal dosing regimens. Better characterization of targets acted upon by CBD in MS should be obtained in ex vivo/in vitro studies in human immune cells, and higher doses should be tested in well-designed clinical trials with clinically relevant efficacy endpoints. [Figure: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11481-021-09982-7. |
format | Online Article Text |
id | pubmed-7829325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-78293252021-01-25 Immunomodulatory Potential of Cannabidiol in Multiple Sclerosis: a Systematic Review Furgiuele, Alessia Cosentino, Marco Ferrari, Marco Marino, Franca J Neuroimmune Pharmacol Invited Review Multiple sclerosis (MS) is the most common chronic autoimmune disease of the central nervous system. Efficacy of treatments for MS is associated with risk of adverse effects, and effective and well-tolerated drugs remain a major unmet need. Cannabis (Cannabis sativa L., fam. Cannabaceae) and cannabinoids are popular among MS patients to treat spasticity and pain. Cannabinoids are endowed with remarkable immunomodulating properties, and in particular the non-psychotropic cannabinoid cannabidiol (CBD) is increasingly recognized as anti-inflammatory and immunosuppressive, nevertheless with excellent tolerability even at high doses. In this systematic review, we retrieved and critically evaluated available evidence regarding the immune and disease-modifying effects of CBD in experimental autoimmune encephalomyelitis (EAE) and in MS. Evidence in rodent models of EAE strongly supports CBD as effective, while clinical evidence is still limited and usually negative, due to paucity of studies and possibly to the use of suboptimal dosing regimens. Better characterization of targets acted upon by CBD in MS should be obtained in ex vivo/in vitro studies in human immune cells, and higher doses should be tested in well-designed clinical trials with clinically relevant efficacy endpoints. [Figure: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11481-021-09982-7. Springer US 2021-01-25 2021 /pmc/articles/PMC7829325/ /pubmed/33492630 http://dx.doi.org/10.1007/s11481-021-09982-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Invited Review Furgiuele, Alessia Cosentino, Marco Ferrari, Marco Marino, Franca Immunomodulatory Potential of Cannabidiol in Multiple Sclerosis: a Systematic Review |
title | Immunomodulatory Potential of Cannabidiol in Multiple Sclerosis: a Systematic Review |
title_full | Immunomodulatory Potential of Cannabidiol in Multiple Sclerosis: a Systematic Review |
title_fullStr | Immunomodulatory Potential of Cannabidiol in Multiple Sclerosis: a Systematic Review |
title_full_unstemmed | Immunomodulatory Potential of Cannabidiol in Multiple Sclerosis: a Systematic Review |
title_short | Immunomodulatory Potential of Cannabidiol in Multiple Sclerosis: a Systematic Review |
title_sort | immunomodulatory potential of cannabidiol in multiple sclerosis: a systematic review |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829325/ https://www.ncbi.nlm.nih.gov/pubmed/33492630 http://dx.doi.org/10.1007/s11481-021-09982-7 |
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