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The Meaning of Immune Reconstitution after Alemtuzumab Therapy in Multiple Sclerosis

Alemtuzumab is a monoclonal antibody that binds to CD52, a protein present on the surface of mature lymphocytes, but not on the stem cells from which these lymphocytes are derived. It is currently used as an immune reconstitution therapy in patients with relapsing–remitting multiple sclerosis. Alemt...

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Detalles Bibliográficos
Autores principales: Rolla, Simona, Maglione, Alessandro, De Mercanti, Stefania Federica, Clerico, Marinella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348777/
https://www.ncbi.nlm.nih.gov/pubmed/32503344
http://dx.doi.org/10.3390/cells9061396
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author Rolla, Simona
Maglione, Alessandro
De Mercanti, Stefania Federica
Clerico, Marinella
author_facet Rolla, Simona
Maglione, Alessandro
De Mercanti, Stefania Federica
Clerico, Marinella
author_sort Rolla, Simona
collection PubMed
description Alemtuzumab is a monoclonal antibody that binds to CD52, a protein present on the surface of mature lymphocytes, but not on the stem cells from which these lymphocytes are derived. It is currently used as an immune reconstitution therapy in patients with relapsing–remitting multiple sclerosis. Alemtuzumab treatment is an intermittent infusion that induces long-term remission of Multiple Sclerosis also in the treatment-free period. After the robust T and B cell depletion induced by alemtuzumab, the immune system undergoes radical changes during its reconstitution. In this review, we will discuss the current knowledge on the reconstitution of the lymphocyte repertoire after alemtuzumab treatment and how it could affect the development of side effects, which led to its temporary suspension by the European Medical Agency.
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spelling pubmed-73487772020-07-20 The Meaning of Immune Reconstitution after Alemtuzumab Therapy in Multiple Sclerosis Rolla, Simona Maglione, Alessandro De Mercanti, Stefania Federica Clerico, Marinella Cells Review Alemtuzumab is a monoclonal antibody that binds to CD52, a protein present on the surface of mature lymphocytes, but not on the stem cells from which these lymphocytes are derived. It is currently used as an immune reconstitution therapy in patients with relapsing–remitting multiple sclerosis. Alemtuzumab treatment is an intermittent infusion that induces long-term remission of Multiple Sclerosis also in the treatment-free period. After the robust T and B cell depletion induced by alemtuzumab, the immune system undergoes radical changes during its reconstitution. In this review, we will discuss the current knowledge on the reconstitution of the lymphocyte repertoire after alemtuzumab treatment and how it could affect the development of side effects, which led to its temporary suspension by the European Medical Agency. MDPI 2020-06-03 /pmc/articles/PMC7348777/ /pubmed/32503344 http://dx.doi.org/10.3390/cells9061396 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rolla, Simona
Maglione, Alessandro
De Mercanti, Stefania Federica
Clerico, Marinella
The Meaning of Immune Reconstitution after Alemtuzumab Therapy in Multiple Sclerosis
title The Meaning of Immune Reconstitution after Alemtuzumab Therapy in Multiple Sclerosis
title_full The Meaning of Immune Reconstitution after Alemtuzumab Therapy in Multiple Sclerosis
title_fullStr The Meaning of Immune Reconstitution after Alemtuzumab Therapy in Multiple Sclerosis
title_full_unstemmed The Meaning of Immune Reconstitution after Alemtuzumab Therapy in Multiple Sclerosis
title_short The Meaning of Immune Reconstitution after Alemtuzumab Therapy in Multiple Sclerosis
title_sort meaning of immune reconstitution after alemtuzumab therapy in multiple sclerosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348777/
https://www.ncbi.nlm.nih.gov/pubmed/32503344
http://dx.doi.org/10.3390/cells9061396
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