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Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration

AMD3100 (plerixafor, Mozobil®) was first identified as an anti-HIV agent specifically active against the T4-lymphotropic HIV strains, as it selectively blocked the CXCR4 receptor. Through interference with the interaction of CXCR4 with its natural ligand, SDF-1 (also named CXCL12), it also mobilized...

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Autor principal: De Clercq, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379795/
https://www.ncbi.nlm.nih.gov/pubmed/30776910
http://dx.doi.org/10.1177/2040206619829382
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author De Clercq, Erik
author_facet De Clercq, Erik
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description AMD3100 (plerixafor, Mozobil®) was first identified as an anti-HIV agent specifically active against the T4-lymphotropic HIV strains, as it selectively blocked the CXCR4 receptor. Through interference with the interaction of CXCR4 with its natural ligand, SDF-1 (also named CXCL12), it also mobilized the CD34(+)stem cells from the bone marrow into the peripheral blood stream. In December 2008, AMD3100 was formally approved by the US FDA for autologous transplantation in patients with Non-Hodgkin’s Lymphoma or multiple myeloma. It may be beneficially used in various other malignant diseases as well as hereditary immunological disorders such as WHIM syndrome, and physiopathological processes such as hepatopulmonary syndrome.
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spelling pubmed-63797952019-02-22 Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration De Clercq, Erik Antivir Chem Chemother Review Article AMD3100 (plerixafor, Mozobil®) was first identified as an anti-HIV agent specifically active against the T4-lymphotropic HIV strains, as it selectively blocked the CXCR4 receptor. Through interference with the interaction of CXCR4 with its natural ligand, SDF-1 (also named CXCL12), it also mobilized the CD34(+)stem cells from the bone marrow into the peripheral blood stream. In December 2008, AMD3100 was formally approved by the US FDA for autologous transplantation in patients with Non-Hodgkin’s Lymphoma or multiple myeloma. It may be beneficially used in various other malignant diseases as well as hereditary immunological disorders such as WHIM syndrome, and physiopathological processes such as hepatopulmonary syndrome. SAGE Publications 2019-02-18 /pmc/articles/PMC6379795/ /pubmed/30776910 http://dx.doi.org/10.1177/2040206619829382 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review Article
De Clercq, Erik
Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration
title Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration
title_full Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration
title_fullStr Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration
title_full_unstemmed Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration
title_short Mozobil® (Plerixafor, AMD3100), 10 years after its approval by the US Food and Drug Administration
title_sort mozobil® (plerixafor, amd3100), 10 years after its approval by the us food and drug administration
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379795/
https://www.ncbi.nlm.nih.gov/pubmed/30776910
http://dx.doi.org/10.1177/2040206619829382
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