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Current utilization of interferon alpha for the treatment of coronavirus disease 2019: A comprehensive review
Recent studies have identified an association between perturbed type I interferon (IFN) responses and the severity of coronavirus disease 2019 (COVID-19). IFNα intervention may normalize the dysregulated innate immunity of COVID-19. However, details regarding its utilization and therapeutic evidence...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755267/ https://www.ncbi.nlm.nih.gov/pubmed/35115233 http://dx.doi.org/10.1016/j.cytogfr.2022.01.001 |
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author | Lu, Ling-Ying Feng, Po-Hao Yu, Ming-Sun Chen, Min-Chi Lin, Alex Jia-Hong Chen, Justin L. Yu, Lennex Hsueh-Lin |
author_facet | Lu, Ling-Ying Feng, Po-Hao Yu, Ming-Sun Chen, Min-Chi Lin, Alex Jia-Hong Chen, Justin L. Yu, Lennex Hsueh-Lin |
author_sort | Lu, Ling-Ying |
collection | PubMed |
description | Recent studies have identified an association between perturbed type I interferon (IFN) responses and the severity of coronavirus disease 2019 (COVID-19). IFNα intervention may normalize the dysregulated innate immunity of COVID-19. However, details regarding its utilization and therapeutic evidence have yet to be systematically evaluated. The aim of this comprehensive review was to summarize the current utilization of IFNα for COVID-19 treatment and to explore the evidence on safety and efficacy. A comprehensive review of clinical studies in the literature prior to December 1st(,) 2021, was performed to identify the current utilization of IFNα, which included details on the route of administration, the number of patients who received the treatment, the severity at the initiation of treatment, age range, the time from the onset of symptoms to treatment, dose, frequency, and duration as well as safety and efficacy. Encouragingly, no evidence was found against the safety of IFNα treatment for COVID-19. Early intervention, either within five days from the onset of symptoms or at hospital admission, confers better clinical outcomes, whereas late intervention may result in prolonged hospitalization. |
format | Online Article Text |
id | pubmed-8755267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Author(s). Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87552672022-01-13 Current utilization of interferon alpha for the treatment of coronavirus disease 2019: A comprehensive review Lu, Ling-Ying Feng, Po-Hao Yu, Ming-Sun Chen, Min-Chi Lin, Alex Jia-Hong Chen, Justin L. Yu, Lennex Hsueh-Lin Cytokine Growth Factor Rev Article Recent studies have identified an association between perturbed type I interferon (IFN) responses and the severity of coronavirus disease 2019 (COVID-19). IFNα intervention may normalize the dysregulated innate immunity of COVID-19. However, details regarding its utilization and therapeutic evidence have yet to be systematically evaluated. The aim of this comprehensive review was to summarize the current utilization of IFNα for COVID-19 treatment and to explore the evidence on safety and efficacy. A comprehensive review of clinical studies in the literature prior to December 1st(,) 2021, was performed to identify the current utilization of IFNα, which included details on the route of administration, the number of patients who received the treatment, the severity at the initiation of treatment, age range, the time from the onset of symptoms to treatment, dose, frequency, and duration as well as safety and efficacy. Encouragingly, no evidence was found against the safety of IFNα treatment for COVID-19. Early intervention, either within five days from the onset of symptoms or at hospital admission, confers better clinical outcomes, whereas late intervention may result in prolonged hospitalization. The Author(s). Published by Elsevier Ltd. 2022-02 2022-01-13 /pmc/articles/PMC8755267/ /pubmed/35115233 http://dx.doi.org/10.1016/j.cytogfr.2022.01.001 Text en © 2022 The Authors 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 Lu, Ling-Ying Feng, Po-Hao Yu, Ming-Sun Chen, Min-Chi Lin, Alex Jia-Hong Chen, Justin L. Yu, Lennex Hsueh-Lin Current utilization of interferon alpha for the treatment of coronavirus disease 2019: A comprehensive review |
title | Current utilization of interferon alpha for the treatment of coronavirus disease 2019: A comprehensive review |
title_full | Current utilization of interferon alpha for the treatment of coronavirus disease 2019: A comprehensive review |
title_fullStr | Current utilization of interferon alpha for the treatment of coronavirus disease 2019: A comprehensive review |
title_full_unstemmed | Current utilization of interferon alpha for the treatment of coronavirus disease 2019: A comprehensive review |
title_short | Current utilization of interferon alpha for the treatment of coronavirus disease 2019: A comprehensive review |
title_sort | current utilization of interferon alpha for the treatment of coronavirus disease 2019: a comprehensive review |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755267/ https://www.ncbi.nlm.nih.gov/pubmed/35115233 http://dx.doi.org/10.1016/j.cytogfr.2022.01.001 |
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