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Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19()
The emergence of SARS-CoV-2, and the ensuing global pandemic, has resulted in an unprecedented response to identify therapies that can limit uncontrolled inflammation observed in patients with moderate to severe COVID-19. The immune pathology behind COVID-19 is complex and involves the activation an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233062/ https://www.ncbi.nlm.nih.gov/pubmed/34182016 http://dx.doi.org/10.1016/j.addr.2021.113848 |
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author | Brain, Danielle Plant-Hately, Alex Heaton, Bethany Arshad, Usman David, Christopher Hedrich, Christian Owen, Andrew Liptrott, Neill J. |
author_facet | Brain, Danielle Plant-Hately, Alex Heaton, Bethany Arshad, Usman David, Christopher Hedrich, Christian Owen, Andrew Liptrott, Neill J. |
author_sort | Brain, Danielle |
collection | PubMed |
description | The emergence of SARS-CoV-2, and the ensuing global pandemic, has resulted in an unprecedented response to identify therapies that can limit uncontrolled inflammation observed in patients with moderate to severe COVID-19. The immune pathology behind COVID-19 is complex and involves the activation and interaction of multiple systems including, but not limited to, complement, inflammasomes, endothelial as well as innate and adaptive immune cells to bring about a convoluted profile of inflammation, coagulation and tissue damage. To date, therapeutic approaches have focussed on inhibition of coagulation, untargeted immune suppression and/or cytokine-directed blocking agents. Regardless of recently achieved improvements in individual patient outcomes and survival rates, improved and focussed approaches targeting individual systems involved is needed to further improve prognosis and wellbeing. This review summarizes the current understanding of molecular and cellular systems involved in the pathophysiology of COVID-19, and their contribution to pathogen clearance and damage to then discuss possible therapeutic options involving immunomodulatory drug delivery systems as well as summarising the complex interplay between them. |
format | Online Article Text |
id | pubmed-8233062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82330622021-06-28 Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19() Brain, Danielle Plant-Hately, Alex Heaton, Bethany Arshad, Usman David, Christopher Hedrich, Christian Owen, Andrew Liptrott, Neill J. Adv Drug Deliv Rev Article The emergence of SARS-CoV-2, and the ensuing global pandemic, has resulted in an unprecedented response to identify therapies that can limit uncontrolled inflammation observed in patients with moderate to severe COVID-19. The immune pathology behind COVID-19 is complex and involves the activation and interaction of multiple systems including, but not limited to, complement, inflammasomes, endothelial as well as innate and adaptive immune cells to bring about a convoluted profile of inflammation, coagulation and tissue damage. To date, therapeutic approaches have focussed on inhibition of coagulation, untargeted immune suppression and/or cytokine-directed blocking agents. Regardless of recently achieved improvements in individual patient outcomes and survival rates, improved and focussed approaches targeting individual systems involved is needed to further improve prognosis and wellbeing. This review summarizes the current understanding of molecular and cellular systems involved in the pathophysiology of COVID-19, and their contribution to pathogen clearance and damage to then discuss possible therapeutic options involving immunomodulatory drug delivery systems as well as summarising the complex interplay between them. Elsevier B.V. 2021-11 2021-06-25 /pmc/articles/PMC8233062/ /pubmed/34182016 http://dx.doi.org/10.1016/j.addr.2021.113848 Text en © 2021 Elsevier B.V. All rights reserved. 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 | Article Brain, Danielle Plant-Hately, Alex Heaton, Bethany Arshad, Usman David, Christopher Hedrich, Christian Owen, Andrew Liptrott, Neill J. Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19() |
title | Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19() |
title_full | Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19() |
title_fullStr | Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19() |
title_full_unstemmed | Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19() |
title_short | Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19() |
title_sort | drug delivery systems as immunomodulators for therapy of infectious disease: relevance to covid-19() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233062/ https://www.ncbi.nlm.nih.gov/pubmed/34182016 http://dx.doi.org/10.1016/j.addr.2021.113848 |
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