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Brain gene therapy with Trojan horse lipid nanoparticles

The COVID-19 mRNA vaccine was developed by the scalable manufacture of lipid nanoparticles (LNPs) that encapsulate mRNA within the lipid. There are many potential applications for this large nucleic acid delivery technology, including the delivery of plasmid DNA for gene therapy. However, gene thera...

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Detalles Bibliográficos
Autor principal: Pardridge, William M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10005896/
https://www.ncbi.nlm.nih.gov/pubmed/36907687
http://dx.doi.org/10.1016/j.molmed.2023.02.004
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author Pardridge, William M.
author_facet Pardridge, William M.
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description The COVID-19 mRNA vaccine was developed by the scalable manufacture of lipid nanoparticles (LNPs) that encapsulate mRNA within the lipid. There are many potential applications for this large nucleic acid delivery technology, including the delivery of plasmid DNA for gene therapy. However, gene therapy for the brain requires LNP delivery across the blood–brain barrier (BBB). It is proposed that LNPs could be reformulated for brain delivery by conjugation of receptor-specific monoclonal antibodies (MAbs) to the LNP surface. The MAb acts as a molecular Trojan horse to trigger receptor-mediated transcytosis (RMT) of the LNP across the BBB and subsequent localization to the nucleus for transcription of the therapeutic gene. Trojan horse LNPs could enable new approaches to gene therapy of the brain.
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spelling pubmed-100058962023-03-13 Brain gene therapy with Trojan horse lipid nanoparticles Pardridge, William M. Trends Mol Med Opinion The COVID-19 mRNA vaccine was developed by the scalable manufacture of lipid nanoparticles (LNPs) that encapsulate mRNA within the lipid. There are many potential applications for this large nucleic acid delivery technology, including the delivery of plasmid DNA for gene therapy. However, gene therapy for the brain requires LNP delivery across the blood–brain barrier (BBB). It is proposed that LNPs could be reformulated for brain delivery by conjugation of receptor-specific monoclonal antibodies (MAbs) to the LNP surface. The MAb acts as a molecular Trojan horse to trigger receptor-mediated transcytosis (RMT) of the LNP across the BBB and subsequent localization to the nucleus for transcription of the therapeutic gene. Trojan horse LNPs could enable new approaches to gene therapy of the brain. The Author(s). Published by Elsevier Ltd. 2023-05 2023-03-11 /pmc/articles/PMC10005896/ /pubmed/36907687 http://dx.doi.org/10.1016/j.molmed.2023.02.004 Text en © 2023 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Opinion
Pardridge, William M.
Brain gene therapy with Trojan horse lipid nanoparticles
title Brain gene therapy with Trojan horse lipid nanoparticles
title_full Brain gene therapy with Trojan horse lipid nanoparticles
title_fullStr Brain gene therapy with Trojan horse lipid nanoparticles
title_full_unstemmed Brain gene therapy with Trojan horse lipid nanoparticles
title_short Brain gene therapy with Trojan horse lipid nanoparticles
title_sort brain gene therapy with trojan horse lipid nanoparticles
topic Opinion
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10005896/
https://www.ncbi.nlm.nih.gov/pubmed/36907687
http://dx.doi.org/10.1016/j.molmed.2023.02.004
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