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Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial
Type 1 Interferons (IFNs) have been associated with positive effects on Coronaviruses. Previous studies point towards the superior potency of IFNβ compared to IFNα against viral infections. We conducted a three-armed, individually-randomized, open-label, controlled trial of IFNβ1a and IFNβ1b, compar...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044200/ https://www.ncbi.nlm.nih.gov/pubmed/33850184 http://dx.doi.org/10.1038/s41598-021-86859-y |
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author | Alavi Darazam, Ilad Shokouhi, Shervin Pourhoseingholi, Mohamad Amin Naghibi Irvani, Seyed Sina Mokhtari, Majid Shabani, Minoosh Amirdosara, Mahdi Torabinavid, Parham Golmohammadi, Maryam Hashemi, SayedPayam Azimi, Arsalan Jafarazadeh Maivan, Mohammad Hossein Rezaei, Omidvar Zali, Alireza Hajiesmaeili, Mohammadreza Shabanpour Dehbsneh, Hadiseh Hoseyni Kusha, Akram Taleb Shoushtari, Maryam Khalili, Negar Soleymaninia, Azam Gachkar, Latif Khoshkar, Ali |
author_facet | Alavi Darazam, Ilad Shokouhi, Shervin Pourhoseingholi, Mohamad Amin Naghibi Irvani, Seyed Sina Mokhtari, Majid Shabani, Minoosh Amirdosara, Mahdi Torabinavid, Parham Golmohammadi, Maryam Hashemi, SayedPayam Azimi, Arsalan Jafarazadeh Maivan, Mohammad Hossein Rezaei, Omidvar Zali, Alireza Hajiesmaeili, Mohammadreza Shabanpour Dehbsneh, Hadiseh Hoseyni Kusha, Akram Taleb Shoushtari, Maryam Khalili, Negar Soleymaninia, Azam Gachkar, Latif Khoshkar, Ali |
author_sort | Alavi Darazam, Ilad |
collection | PubMed |
description | Type 1 Interferons (IFNs) have been associated with positive effects on Coronaviruses. Previous studies point towards the superior potency of IFNβ compared to IFNα against viral infections. We conducted a three-armed, individually-randomized, open-label, controlled trial of IFNβ1a and IFNβ1b, comparing them against each other and a control group. Patients were randomly assigned in a 1:1:1 ratio to IFNβ1a (subcutaneous injections of 12,000 IU on days 1, 3, 6), IFNβ1b (subcutaneous injections of 8,000,000 IU on days 1, 3, 6), or the control group. All three arms orally received Lopinavir/Ritonavir (400 mg/100 mg twice a day for ten days) and a single dose of Hydroxychloroquine 400 mg on the first day. Our utilized primary outcome measure was Time To Clinical Improvement (TTCI) defined as the time from enrollment to discharge or a decline of two steps on the clinical seven-step ordinal scale, whichsoever came first. A total of 60 severely ill patients with positive RT-PCR and Chest CT scans underwent randomization (20 patients to each arm). In the Intention-To-Treat population, IFNβ1a was associated with a significant difference against the control group, in the TTCI; (HR; 2.36, 95% CI 1.10–5.17, P-value = 0.031) while the IFNβ1b indicated no significant difference compared with the control; HR; 1.42, (95% CI 0.63–3.16, P-value = 0.395). The median TTCI for both of the intervention groups was five days vs. seven days for the control group. The mortality was numerically lower in both of the intervention groups (20% in the IFNβ1a group and 30% in the IFNβ1b group vs. 45% in the control group). There were no significant differences between the three arms regarding the adverse events. In patients with laboratory-confirmed SARS-CoV-2 infection, as compared with the base therapeutic regiment, the benefit of a significant reduction in TTCI was observed in the IFNβ1a arm. This finding needs further confirmation in larger studies. Trial Registration Number: ClinicalTrials.gov, NCT04343768. (Submitted: 08/04/2020; First Online: 13/04/2020) (Registration Number: NCT04343768). |
format | Online Article Text |
id | pubmed-8044200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80442002021-04-14 Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial Alavi Darazam, Ilad Shokouhi, Shervin Pourhoseingholi, Mohamad Amin Naghibi Irvani, Seyed Sina Mokhtari, Majid Shabani, Minoosh Amirdosara, Mahdi Torabinavid, Parham Golmohammadi, Maryam Hashemi, SayedPayam Azimi, Arsalan Jafarazadeh Maivan, Mohammad Hossein Rezaei, Omidvar Zali, Alireza Hajiesmaeili, Mohammadreza Shabanpour Dehbsneh, Hadiseh Hoseyni Kusha, Akram Taleb Shoushtari, Maryam Khalili, Negar Soleymaninia, Azam Gachkar, Latif Khoshkar, Ali Sci Rep Article Type 1 Interferons (IFNs) have been associated with positive effects on Coronaviruses. Previous studies point towards the superior potency of IFNβ compared to IFNα against viral infections. We conducted a three-armed, individually-randomized, open-label, controlled trial of IFNβ1a and IFNβ1b, comparing them against each other and a control group. Patients were randomly assigned in a 1:1:1 ratio to IFNβ1a (subcutaneous injections of 12,000 IU on days 1, 3, 6), IFNβ1b (subcutaneous injections of 8,000,000 IU on days 1, 3, 6), or the control group. All three arms orally received Lopinavir/Ritonavir (400 mg/100 mg twice a day for ten days) and a single dose of Hydroxychloroquine 400 mg on the first day. Our utilized primary outcome measure was Time To Clinical Improvement (TTCI) defined as the time from enrollment to discharge or a decline of two steps on the clinical seven-step ordinal scale, whichsoever came first. A total of 60 severely ill patients with positive RT-PCR and Chest CT scans underwent randomization (20 patients to each arm). In the Intention-To-Treat population, IFNβ1a was associated with a significant difference against the control group, in the TTCI; (HR; 2.36, 95% CI 1.10–5.17, P-value = 0.031) while the IFNβ1b indicated no significant difference compared with the control; HR; 1.42, (95% CI 0.63–3.16, P-value = 0.395). The median TTCI for both of the intervention groups was five days vs. seven days for the control group. The mortality was numerically lower in both of the intervention groups (20% in the IFNβ1a group and 30% in the IFNβ1b group vs. 45% in the control group). There were no significant differences between the three arms regarding the adverse events. In patients with laboratory-confirmed SARS-CoV-2 infection, as compared with the base therapeutic regiment, the benefit of a significant reduction in TTCI was observed in the IFNβ1a arm. This finding needs further confirmation in larger studies. Trial Registration Number: ClinicalTrials.gov, NCT04343768. (Submitted: 08/04/2020; First Online: 13/04/2020) (Registration Number: NCT04343768). Nature Publishing Group UK 2021-04-13 /pmc/articles/PMC8044200/ /pubmed/33850184 http://dx.doi.org/10.1038/s41598-021-86859-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Alavi Darazam, Ilad Shokouhi, Shervin Pourhoseingholi, Mohamad Amin Naghibi Irvani, Seyed Sina Mokhtari, Majid Shabani, Minoosh Amirdosara, Mahdi Torabinavid, Parham Golmohammadi, Maryam Hashemi, SayedPayam Azimi, Arsalan Jafarazadeh Maivan, Mohammad Hossein Rezaei, Omidvar Zali, Alireza Hajiesmaeili, Mohammadreza Shabanpour Dehbsneh, Hadiseh Hoseyni Kusha, Akram Taleb Shoushtari, Maryam Khalili, Negar Soleymaninia, Azam Gachkar, Latif Khoshkar, Ali Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial |
title | Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial |
title_full | Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial |
title_fullStr | Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial |
title_full_unstemmed | Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial |
title_short | Role of interferon therapy in severe COVID-19: the COVIFERON randomized controlled trial |
title_sort | role of interferon therapy in severe covid-19: the coviferon randomized controlled trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8044200/ https://www.ncbi.nlm.nih.gov/pubmed/33850184 http://dx.doi.org/10.1038/s41598-021-86859-y |
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