Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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
_version_ 1783678436694294528
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
work_keys_str_mv AT alavidarazamilad roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT shokouhishervin roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT pourhoseingholimohamadamin roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT naghibiirvaniseyedsina roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT mokhtarimajid roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT shabaniminoosh roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT amirdosaramahdi roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT torabinavidparham roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT golmohammadimaryam roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT hashemisayedpayam roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT azimiarsalan roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT jafarazadehmaivanmohammadhossein roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT rezaeiomidvar roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT zalialireza roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT hajiesmaeilimohammadreza roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT shabanpourdehbsnehhadiseh roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT hoseynikushaakram roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT talebshoushtarimaryam roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT khalilinegar roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT soleymaniniaazam roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT gachkarlatif roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial
AT khoshkarali roleofinterferontherapyinseverecovid19thecoviferonrandomizedcontrolledtrial