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Immunomodulatory therapies for SARS-CoV-2 infection: a systematic literature review to inform EULAR points to consider
OBJECTIVE: To summarise the available information on efficacy and safety of immunomodulatory agents in SARS-CoV-2 infection. METHODS: As part of a European League Against Rheumatism (EULAR) taskforce, a systematic literature search was conducted from January 2019 to 11 December 2020. Two reviewers i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142448/ https://www.ncbi.nlm.nih.gov/pubmed/33589438 http://dx.doi.org/10.1136/annrheumdis-2020-219725 |
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author | Alunno, Alessia Najm, Aurélie Mariette, Xavier De Marco, Gabriele Emmel, Jenny Mason, Laura McGonagle, Dennis G Machado, Pedro M |
author_facet | Alunno, Alessia Najm, Aurélie Mariette, Xavier De Marco, Gabriele Emmel, Jenny Mason, Laura McGonagle, Dennis G Machado, Pedro M |
author_sort | Alunno, Alessia |
collection | PubMed |
description | OBJECTIVE: To summarise the available information on efficacy and safety of immunomodulatory agents in SARS-CoV-2 infection. METHODS: As part of a European League Against Rheumatism (EULAR) taskforce, a systematic literature search was conducted from January 2019 to 11 December 2020. Two reviewers independently identified eligible studies according to the Population, Intervention, Comparator and Outcome framework and extracted data on efficacy and safety of immunomodulatory agents used therapeutically in SARS-CoV-2 infection at any stage. The risk of bias was assessed with validated tools. RESULTS: Of the 60 372 records, 401 articles were eligible for inclusion. Studies were at variable risk of bias. Randomised controlled trials (RCTs) were available for the following drugs: hydroxychloroquine (n=12), glucocorticoids (n=6), tocilizumab (n=4), convalescent plasma (n=4), interferon beta (n=2), intravenous immunoglobulins (IVIg) (n=2) and n=1 each for anakinra, baricitinib, colchicine, leflunomide, ruxolitinib, interferon kappa and vilobelimab. Glucocorticoids were able to reduce mortality in specific subsets of patients, while conflicting data were available about tocilizumab. Hydroxychloroquine was not beneficial at any disease stage, one RCT with anakinra was negative, one RCT with baricitinib+remdesivir was positive, and individual trials on some other compounds provided interesting, although preliminary, results. CONCLUSION: Although there is emerging evidence about immunomodulatory therapies for the management of COVID-19, conclusive data are scarce with some conflicting data. Since glucocorticoids seem to improve survival in some subsets of patients, RCTs comparing glucocorticoids alone versus glucocorticoids plus anticytokine/immunomodulatory treatment are warranted. This systematic literature review informed the initiative to formulate EULAR ‘points to consider’ on COVID-19 pathophysiology and immunomodulatory treatment from the rheumatology perspective. |
format | Online Article Text |
id | pubmed-8142448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-81424482021-06-07 Immunomodulatory therapies for SARS-CoV-2 infection: a systematic literature review to inform EULAR points to consider Alunno, Alessia Najm, Aurélie Mariette, Xavier De Marco, Gabriele Emmel, Jenny Mason, Laura McGonagle, Dennis G Machado, Pedro M Ann Rheum Dis Epidemiology OBJECTIVE: To summarise the available information on efficacy and safety of immunomodulatory agents in SARS-CoV-2 infection. METHODS: As part of a European League Against Rheumatism (EULAR) taskforce, a systematic literature search was conducted from January 2019 to 11 December 2020. Two reviewers independently identified eligible studies according to the Population, Intervention, Comparator and Outcome framework and extracted data on efficacy and safety of immunomodulatory agents used therapeutically in SARS-CoV-2 infection at any stage. The risk of bias was assessed with validated tools. RESULTS: Of the 60 372 records, 401 articles were eligible for inclusion. Studies were at variable risk of bias. Randomised controlled trials (RCTs) were available for the following drugs: hydroxychloroquine (n=12), glucocorticoids (n=6), tocilizumab (n=4), convalescent plasma (n=4), interferon beta (n=2), intravenous immunoglobulins (IVIg) (n=2) and n=1 each for anakinra, baricitinib, colchicine, leflunomide, ruxolitinib, interferon kappa and vilobelimab. Glucocorticoids were able to reduce mortality in specific subsets of patients, while conflicting data were available about tocilizumab. Hydroxychloroquine was not beneficial at any disease stage, one RCT with anakinra was negative, one RCT with baricitinib+remdesivir was positive, and individual trials on some other compounds provided interesting, although preliminary, results. CONCLUSION: Although there is emerging evidence about immunomodulatory therapies for the management of COVID-19, conclusive data are scarce with some conflicting data. Since glucocorticoids seem to improve survival in some subsets of patients, RCTs comparing glucocorticoids alone versus glucocorticoids plus anticytokine/immunomodulatory treatment are warranted. This systematic literature review informed the initiative to formulate EULAR ‘points to consider’ on COVID-19 pathophysiology and immunomodulatory treatment from the rheumatology perspective. BMJ Publishing Group 2021-06 2021-02-15 /pmc/articles/PMC8142448/ /pubmed/33589438 http://dx.doi.org/10.1136/annrheumdis-2020-219725 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Epidemiology Alunno, Alessia Najm, Aurélie Mariette, Xavier De Marco, Gabriele Emmel, Jenny Mason, Laura McGonagle, Dennis G Machado, Pedro M Immunomodulatory therapies for SARS-CoV-2 infection: a systematic literature review to inform EULAR points to consider |
title | Immunomodulatory therapies for SARS-CoV-2 infection: a systematic literature review to inform EULAR points to consider |
title_full | Immunomodulatory therapies for SARS-CoV-2 infection: a systematic literature review to inform EULAR points to consider |
title_fullStr | Immunomodulatory therapies for SARS-CoV-2 infection: a systematic literature review to inform EULAR points to consider |
title_full_unstemmed | Immunomodulatory therapies for SARS-CoV-2 infection: a systematic literature review to inform EULAR points to consider |
title_short | Immunomodulatory therapies for SARS-CoV-2 infection: a systematic literature review to inform EULAR points to consider |
title_sort | immunomodulatory therapies for sars-cov-2 infection: a systematic literature review to inform eular points to consider |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142448/ https://www.ncbi.nlm.nih.gov/pubmed/33589438 http://dx.doi.org/10.1136/annrheumdis-2020-219725 |
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