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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Type 1 interferons as a potential treatment against COVID-19</title>
<author><name sortKey="Sallard, Erwan" sort="Sallard, Erwan" uniqKey="Sallard E" first="Erwan" last="Sallard">Erwan Sallard</name>
<affiliation><nlm:aff id="aff1">École Normale Supérieure de Paris, 45 Rue D'Ulm, 75005, Paris, France</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Lescure, Francois Xavier" sort="Lescure, Francois Xavier" uniqKey="Lescure F" first="François-Xavier" last="Lescure">François-Xavier Lescure</name>
<affiliation><nlm:aff id="aff2">Université de Paris, IAME, INSERM, F-75018, Paris, France</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff3">Department of Infectious and Tropical Diseases, Assistance Publique - Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, 75018, Paris, France</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Yazdanpanah, Yazdan" sort="Yazdanpanah, Yazdan" uniqKey="Yazdanpanah Y" first="Yazdan" last="Yazdanpanah">Yazdan Yazdanpanah</name>
<affiliation><nlm:aff id="aff2">Université de Paris, IAME, INSERM, F-75018, Paris, France</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff3">Department of Infectious and Tropical Diseases, Assistance Publique - Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, 75018, Paris, France</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Mentre, France" sort="Mentre, France" uniqKey="Mentre F" first="France" last="Mentre">France Mentre</name>
<affiliation><nlm:aff id="aff2">Université de Paris, IAME, INSERM, F-75018, Paris, France</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Peiffer Smadja, Nathan" sort="Peiffer Smadja, Nathan" uniqKey="Peiffer Smadja N" first="Nathan" last="Peiffer-Smadja">Nathan Peiffer-Smadja</name>
<affiliation><nlm:aff id="aff2">Université de Paris, IAME, INSERM, F-75018, Paris, France</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff3">Department of Infectious and Tropical Diseases, Assistance Publique - Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, 75018, Paris, France</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">32275914</idno>
<idno type="pmc">7138382</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138382</idno>
<idno type="RBID">PMC:7138382</idno>
<idno type="doi">10.1016/j.antiviral.2020.104791</idno>
<date when="2020">2020</date>
<idno type="wicri:Area/Pmc/Corpus">000827</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000827</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Type 1 interferons as a potential treatment against COVID-19</title>
<author><name sortKey="Sallard, Erwan" sort="Sallard, Erwan" uniqKey="Sallard E" first="Erwan" last="Sallard">Erwan Sallard</name>
<affiliation><nlm:aff id="aff1">École Normale Supérieure de Paris, 45 Rue D'Ulm, 75005, Paris, France</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Lescure, Francois Xavier" sort="Lescure, Francois Xavier" uniqKey="Lescure F" first="François-Xavier" last="Lescure">François-Xavier Lescure</name>
<affiliation><nlm:aff id="aff2">Université de Paris, IAME, INSERM, F-75018, Paris, France</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff3">Department of Infectious and Tropical Diseases, Assistance Publique - Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, 75018, Paris, France</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Yazdanpanah, Yazdan" sort="Yazdanpanah, Yazdan" uniqKey="Yazdanpanah Y" first="Yazdan" last="Yazdanpanah">Yazdan Yazdanpanah</name>
<affiliation><nlm:aff id="aff2">Université de Paris, IAME, INSERM, F-75018, Paris, France</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff3">Department of Infectious and Tropical Diseases, Assistance Publique - Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, 75018, Paris, France</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Mentre, France" sort="Mentre, France" uniqKey="Mentre F" first="France" last="Mentre">France Mentre</name>
<affiliation><nlm:aff id="aff2">Université de Paris, IAME, INSERM, F-75018, Paris, France</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Peiffer Smadja, Nathan" sort="Peiffer Smadja, Nathan" uniqKey="Peiffer Smadja N" first="Nathan" last="Peiffer-Smadja">Nathan Peiffer-Smadja</name>
<affiliation><nlm:aff id="aff2">Université de Paris, IAME, INSERM, F-75018, Paris, France</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff3">Department of Infectious and Tropical Diseases, Assistance Publique - Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, 75018, Paris, France</nlm:aff>
</affiliation>
</author>
</analytic>
<series><title level="j">Antiviral Research</title>
<idno type="ISSN">0166-3542</idno>
<idno type="eISSN">1872-9096</idno>
<imprint><date when="2020">2020</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p>Type 1 interferons have a broad antiviral activity <italic>in vitro</italic>
and are currently evaluated in a clinical trial to treat MERS-CoV. In this review, we discuss preliminary data concerning the potential activity of type 1 interferons on SARS-CoV-2, and the relevance of evaluating these molecules in clinical trials for the treatment of COVID-19.</p>
</div>
</front>
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</TEI>
<pmc article-type="brief-report"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Antiviral Res</journal-id>
<journal-id journal-id-type="iso-abbrev">Antiviral Res</journal-id>
<journal-title-group><journal-title>Antiviral Research</journal-title>
</journal-title-group>
<issn pub-type="ppub">0166-3542</issn>
<issn pub-type="epub">1872-9096</issn>
<publisher><publisher-name>Elsevier B.V.</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">32275914</article-id>
<article-id pub-id-type="pmc">7138382</article-id>
<article-id pub-id-type="publisher-id">S0166-3542(20)30205-9</article-id>
<article-id pub-id-type="doi">10.1016/j.antiviral.2020.104791</article-id>
<article-id pub-id-type="publisher-id">104791</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Type 1 interferons as a potential treatment against COVID-19</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" id="au1"><name><surname>Sallard</surname>
<given-names>Erwan</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author" id="au2"><name><surname>Lescure</surname>
<given-names>François-Xavier</given-names>
</name>
<xref rid="aff2" ref-type="aff">b</xref>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author" id="au3"><name><surname>Yazdanpanah</surname>
<given-names>Yazdan</given-names>
</name>
<xref rid="aff2" ref-type="aff">b</xref>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author" id="au4"><name><surname>Mentre</surname>
<given-names>France</given-names>
</name>
<xref rid="aff2" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author" id="au5"><name><surname>Peiffer-Smadja</surname>
<given-names>Nathan</given-names>
</name>
<email>nathan.peiffer-smadja@inserm.fr</email>
<xref rid="aff2" ref-type="aff">b</xref>
<xref rid="aff3" ref-type="aff">c</xref>
<xref rid="cor1" ref-type="corresp">∗</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>a</label>
École Normale Supérieure de Paris, 45 Rue D'Ulm, 75005, Paris, France</aff>
<aff id="aff2"><label>b</label>
Université de Paris, IAME, INSERM, F-75018, Paris, France</aff>
<aff id="aff3"><label>c</label>
Department of Infectious and Tropical Diseases, Assistance Publique - Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, 75018, Paris, France</aff>
<author-notes><corresp id="cor1"><label>∗</label>
Corresponding author. Department of Infectious and Tropical Diseases, Assistance Publique - Hôpitaux de Paris, Bichat-Claude Bernard University Hospital, 46 Rue Henri Huchard, 75018, Paris, Paris, France. <email>nathan.peiffer-smadja@inserm.fr</email>
</corresp>
</author-notes>
<pub-date pub-type="pmc-release"><day>7</day>
<month>4</month>
<year>2020</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>6</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub"><day>7</day>
<month>4</month>
<year>2020</year>
</pub-date>
<volume>178</volume>
<fpage>104791</fpage>
<lpage>104791</lpage>
<history><date date-type="received"><day>26</day>
<month>3</month>
<year>2020</year>
</date>
<date date-type="accepted"><day>3</day>
<month>4</month>
<year>2020</year>
</date>
</history>
<permissions><copyright-statement>© 2020 Elsevier B.V. All rights reserved.</copyright-statement>
<copyright-year>2020</copyright-year>
<copyright-holder>Elsevier B.V.</copyright-holder>
<license><license-p>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.</license-p>
</license>
</permissions>
<abstract id="abs0010"><p>Type 1 interferons have a broad antiviral activity <italic>in vitro</italic>
and are currently evaluated in a clinical trial to treat MERS-CoV. In this review, we discuss preliminary data concerning the potential activity of type 1 interferons on SARS-CoV-2, and the relevance of evaluating these molecules in clinical trials for the treatment of COVID-19.</p>
</abstract>
<abstract abstract-type="author-highlights" id="abs0015"><title>Highlights</title>
<p><list list-type="simple" id="ulist0010"><list-item id="u0010"><label>•</label>
<p id="p0010">Interferon treatment has shown mixed efficiency against SARS-CoV and MERS-CoV.</p>
</list-item>
<list-item id="u0015"><label>•</label>
<p id="p0015">SARS-CoV-2 is probably more sensitive to interferon than the other coronaviruses.</p>
</list-item>
<list-item id="u0020"><label>•</label>
<p id="p0020">The IFNβ subtype appears to be the most suited for COVID-19 treatment.</p>
</list-item>
<list-item id="u0025"><label>•</label>
<p id="p0025">Interferon treatment should be performed in the early stages of the infection.</p>
</list-item>
<list-item id="u0030"><label>•</label>
<p id="p0030">Investigation on interferon-based COVID-19 treatment is warranted.</p>
</list-item>
</list>
</p>
</abstract>
<kwd-group id="kwrds0010"><title>Keywords</title>
<kwd>Interferon</kwd>
<kwd>COVID-19</kwd>
<kwd>SARS-CoV-2</kwd>
</kwd-group>
</article-meta>
</front>
<body><sec id="sec1"><title>Funding</title>
<p id="p0035">This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.</p>
</sec>
<sec id="sec2"><label>1</label>
<title>Main text</title>
<p id="p0040">SARS-CoV-2 is a human coronavirus causing the COVID-19 disease. It emerged in China in December 2019 and rapidly propagated in numerous countries, having contaminated more than one million people and killing more than 55,000 up to April 3, 2020. Antiviral treatments are warranted to contain the epidemics. Several candidates are already being investigated, including type 1 interferon (IFN–I) (<xref rid="bib24" ref-type="bibr">Martinez, 2020</xref>
; <xref rid="bib5" ref-type="bibr">Belhadi et al., 2020</xref>
). Indeed, in the context of emerging viral infections, IFN-I are often evaluated (usually in combination with other drugs) before specific treatments are developed, due to their unspecific antiviral effects (<xref rid="bib13" ref-type="bibr">Gao et al., 2010</xref>
; <xref rid="bib21" ref-type="bibr">Loutfy et al., 2003</xref>
; <xref rid="bib27" ref-type="bibr">Omrani et al., 2014</xref>
). We aimed to review the evidence supporting the evaluation of IFN-1 in the treatment of coronaviruses and to discuss its potential in SARS-CoV-2.</p>
<p id="p0045">Type 1 interferons (IFN–I) designate a group of cytokines comprising the ubiquitous α and β subtypes (themselves subdivided in several isoforms), as well as the ε, ω and κ subtypes (<xref rid="bib30" ref-type="bibr">Samuel, 2001</xref>
). They are secreted by various cell types, notably plasmacytoid dendritic cells, upon recognition of viral components by pattern recognition receptors (PRR) (<xref rid="bib19" ref-type="bibr">Liu, 2005</xref>
). IFN-I are thus among the first cytokines produced during a viral infection. They are recognized by the IFNAR receptor present at the plasma membrane in most cell types. Interferon fixation on IFNAR induces the phosphorylation of transcriptional factors such as STAT1 and their relocalization to the nucleus, where they activate interferon-stimulated genes (ISG). Most ISGs are involved in inflammation, signaling and immunomodulation. They interfere with viral replication and spread by several mechanisms such as a slowdown of cell metabolism or secretion of cytokines which promote the activation of the adaptive immunity. ISGs include PRRs, which further sensitize the cell to pathogens, proteins which decrease membrane fluidity, preventing viral egress or membrane fusion, and antivirals that specifically inhibit one step of the viral cycle (<xref rid="bib32" ref-type="bibr">Schneider et al., 2014</xref>
; <xref rid="bib39" ref-type="bibr">Totura and Baric, 2012</xref>
). IFN-I thus play a major role in antiviral immunity. Because of their immunomodulatory properties, IFN-I are used in the treatment of numerous diseases: for example, subcutaneous injections of IFNβ have been used for more than 20 years for the treatment of patients with multiple sclerosis. The role of IFNβ in the treatment of multiple sclerosis is still debated and likely results partly from the down-regulation of the major histocompatibility complex (MHC) class II expression in antigen-presenting cells, the induction of IL-10 secretion and the inhibition of T-cell migration (<xref rid="bib16" ref-type="bibr">Jakimovski et al., 2018</xref>
).</p>
<p id="p0050">MERS-CoV and SARS-CoV are coronaviruses closely linked with SARS-CoV-2 and presenting similar properties, despite differences in their epidemiology, pathology and in several of their proteins (<xref rid="bib18" ref-type="bibr">Lai et al., 2020</xref>
). IFN-I treatment has been studied against MERS-CoV and SARS-CoV (reviewed in <xref rid="bib37" ref-type="bibr">Stockman et al., 2006</xref>
), in numerous experiments, both <italic>in vitro</italic>
and <italic>in vivo</italic>
, and in combination or not with lopinavir/ritonavir (<xref rid="bib7" ref-type="bibr">Chan et al., 2015</xref>
; <xref rid="bib34" ref-type="bibr">Sheahan et al., 2020</xref>
), ribavirin (<xref rid="bib9" ref-type="bibr">Chen et al., 2004</xref>
; <xref rid="bib26" ref-type="bibr">Morgenstern et al., 2005</xref>
; <xref rid="bib27" ref-type="bibr">Omrani et al., 2014</xref>
), remdesivir, corticosteroids (<xref rid="bib21" ref-type="bibr">Loutfy et al., 2003</xref>
), or IFNγ (<xref rid="bib29" ref-type="bibr">Sainz et al., 2004</xref>
; <xref rid="bib31" ref-type="bibr">Scagnolari et al., 2004</xref>
). IFNα and β were systematically relatively efficient <italic>in vitro</italic>
and succeeded in certain animal models (<xref rid="bib7" ref-type="bibr">Chan et al., 2015</xref>
), but generally failed to significantly improve the disease in humans (<xref rid="bib37" ref-type="bibr">Stockman et al., 2006</xref>
). For example, a combination of IFNβ with lopinavir/ritonavir against MERS-CoV improved pulmonary function but did not significantly reduce virus replication or lung pathology severity (<xref rid="bib34" ref-type="bibr">Sheahan et al., 2020</xref>
), while a combination of IFNα2a with ribavirin delayed mortality without decreasing it on the long run (<xref rid="bib27" ref-type="bibr">Omrani et al., 2014</xref>
). Similarly, the combination of IFNα2b with ribavirin gave excellent results in the rhesus macaque (<xref rid="bib11" ref-type="bibr">Falzarano et al., 2013</xref>
), but was inconclusive in human (<xref rid="bib2" ref-type="bibr">Arabi et al., 2017</xref>
). The lack of significant disease improvement with IFN-I treatment in numerous studies can be explained by the mechanisms of inhibition of the IFN signaling pathway used by MERS-CoV and SARS-CoV, by the limited number of patients or animals used in the studies, or by the difficulty to decipher whether disease improvements were caused by IFN-I or the drugs used in combination with it. In addition, results often differ substantially between studies because of inconsistencies in the experimental settings or the clinical conditions (<xref rid="bib37" ref-type="bibr">Stockman et al., 2006</xref>
): for example, a study on SARS-CoV revealed a positive effect of IFN-I treatment (<xref rid="bib21" ref-type="bibr">Loutfy et al., 2003</xref>
), while another study with a larger cohort did not detect any significant effect (<xref rid="bib41" ref-type="bibr">Zhao et al., 2003</xref>
). It has also been proposed that interferon was efficient in patients only if they lacked comorbidities (<xref rid="bib1" ref-type="bibr">Al-Tawfiq et al., 2014</xref>
; <xref rid="bib33" ref-type="bibr">Shalhoub et al., 2015</xref>
). Subtype diversity could be another explanation of inconsistencies between studies. It was repeatedly shown that IFNβ is a more potent inhibitor of coronaviruses than IFNα (<xref rid="bib31" ref-type="bibr">Scagnolari et al., 2004</xref>
; <xref rid="bib37" ref-type="bibr">Stockman et al., 2006</xref>
): depending on the studies, IFNβ1b or IFNβ1a were the most potent IFN-I subtype in the inhibition of SARS-CoV (<xref rid="bib15" ref-type="bibr">Hensley et al., 2004</xref>
) and MERS-CoV (<xref rid="bib6" ref-type="bibr">Chan et al., 2013</xref>
; <xref rid="bib10" ref-type="bibr">Dong et al., 2020</xref>
; <xref rid="bib14" ref-type="bibr">Hart et al., 2014</xref>
). Consequently, IFNβ1 appears to be most relevant interferon to treat coronavirus infections. This fact can be related to the protective activity of IFNβ1 in the lung: it up-regulates cluster of differentiation 73 (CD73) in pulmonary endothelial cells, resulting in the secretion of anti-inflammatory adenosine and the maintenance of endothelial barrier function. This process explains why clinical data indicate a reduction of vascular leakage in acute respiratory distress syndrome (ARDS) with IFNβ1a treatment (<xref rid="bib4" ref-type="bibr">Bellingan et al., 2014</xref>
). However, this effect is insufficient to decrease ARDS mortality (<xref rid="bib28" ref-type="bibr">Ranieri et al., 2020</xref>
). It has been suggested from <italic>in vivo</italic>
studies in mice that the timing of IFN-I administration plays a crucial role: positive effects were observed if IFN-I was administered shortly after infection, but IFN-I failed to inhibit viral replication and had side-effects when administered later (<xref rid="bib8" ref-type="bibr">Channappanavar et al., 2019</xref>
). Following a study showing that IFNβ1b was as efficient as lopinavir/ritonavir against MERS-CoV in marmosets (<xref rid="bib7" ref-type="bibr">Chan et al., 2015</xref>
), the combination of IFNβ1b (injected intravenously) and lopinavir/ritonavir is currently investigated in a clinical trial in Saudi Arabia (<xref rid="bib3" ref-type="bibr">Arabi et al., 2018</xref>
). This is to our knowledge the only clinical trial against MERS-CoV.</p>
<p id="p0055">The knowledge gained from experiments of IFN-I treatment against SARS-CoV and MERS-CoV is valuable in the selection of potential treatments against SARS-CoV-2. SARS-CoV and MERS-CoV are able to disrupt the interferon signaling pathway. For example, the Orf6 protein of SARS-CoV disrupts karyopherin transport (<xref rid="bib12" ref-type="bibr">Frieman et al., 2007</xref>
; <xref rid="bib17" ref-type="bibr">Kopecky-Bromberg et al., 2007</xref>
) and consequently inhibits the import in the nucleus of transcriptional factors such as STAT1, resulting in the interferon response. Similarly, the Orf3b protein of SARS-CoV inhibits the phosphorylation of IRF3 (<xref rid="bib17" ref-type="bibr">Kopecky-Bromberg et al., 2007</xref>
), a protein involved in the activation of IFN expression. However, the Orf6 and Orf3b proteins of SARS-CoV-2 are truncated (<xref rid="bib20" ref-type="bibr">Lokugamage et al., 2020</xref>
) and may have lost their anti-interferon functions. It could explain why SARS-CoV-2 displays <italic>in vitro</italic>
a substantial sensitivity to IFNα (<xref rid="bib20" ref-type="bibr">Lokugamage et al., 2020</xref>
): although SARS-CoV-2 replication is not entirely suppressed by interferons, viral titers are decreased by several orders of magnitude. SARS-CoV2 is substantially more sensitive to IFN-I than SARS-CoV, which suggests that IFN-I treatment should be at least as effective for the former than for the latter. Supporting this hypothesis, it was shown that IFNα2b sprays can reduce the infection rate of SARS-CoV-2 (<xref rid="bib35" ref-type="bibr">Shen and Yang, 2020</xref>
). This study shows that IFN-I can be used as a prophylaxis against SARS-CoV-2, which is confirmed by the <italic>in vitro</italic>
efficacy of interferon pretreatment against the virus (<xref rid="bib20" ref-type="bibr">Lokugamage et al., 2020</xref>
), while the replication of MERS-CoV (<xref rid="bib34" ref-type="bibr">Sheahan et al., 2020</xref>
) and SARS-CoV (<xref rid="bib25" ref-type="bibr">Menachery et al., 2014</xref>
; <xref rid="bib38" ref-type="bibr">Thiel and Weber, 2008</xref>
), was reported to be indifferent to IFN-I prophylaxis.</p>
<p id="p0060">From the data presented above, IFN-I might be a safe and efficient treatment against SARS-CoV-2. Knowledge acquired during studies on MERS-CoV or SARS-CoV would be critical assets in that perspective: for example, they indicate that IFNβ should be the most relevant interferon subtype, and that IFN-I should be administered as early as possible to optimize antiviral therapy and avoid adverse events (<xref rid="bib8" ref-type="bibr">Channappanavar et al., 2019</xref>
). Furthermore, COVID-19 pathology, mainly consisting in pulmonary lesions, presents similar characteristics with interferonopathies: it may suggest that SARS-CoV-2 induces an excessive IFN-I mediated antiviral response, leading to tissue damage. IFN-I treatment should be limited to the early phases of the infection if this hypothesis is confirmed, as suggested in (<xref rid="bib36" ref-type="bibr">Siddiqi and Mehra, 2020</xref>
) and by early clinical data showing that inflammatory biomarkers are associated with increased mortality (<xref rid="bib42" ref-type="bibr">Zhou et al., 2020</xref>
). In the late phases, it is even possible that anti-interferon drugs should be used to mitigate the pathology (<xref rid="bib40" ref-type="bibr">Zhang et al., 2020</xref>
).</p>
<p id="p0065">In China, the guidelines for the treatment of COVID-19 recommend to administer 5 million U of IFNα by vapor inhalation twice a day to the patients, in combination with ribavirin (<xref rid="bib10" ref-type="bibr">Dong et al., 2020</xref>
; <xref rid="bib22" ref-type="bibr">Lu, 2020</xref>
). Clinical trials have been recently registered to evaluate a combination of lopinavir/ritonavir and IFNα2b (ChiCTR2000029387) or a combination of lopinavir/ritonavir with ribavirin and IFNβ1b administered subcutanously (NCT04276688) for the treatment of COVID-19. The administration by vapor inhalation currently performed in China offers the advantage of targeting specifically the respiratory tract; however, to the best of our knowledge, the pharmacodynamics and pharmacokinetics of this mode of administration have never been assessed. On the contrary, the intravenous and subcutaneous modes of administration are well-described, have already proven safe in several clinical trials, and have similar pharmacodynamics and pharmacokinetics (<xref rid="bib23" ref-type="bibr">Mager and Jusko, 2002</xref>
). The combination of IFN-I with lopinavir/ritonavir, ribavirin or remdesivir could improve its efficacy, because of the efficiency of such combinations observed <italic>in vitro</italic>
in other coronaviruses (<xref rid="bib34" ref-type="bibr">Sheahan et al., 2020</xref>
). It might also be relevant to evaluate type III IFN for the treatment of COVID-19 (<xref rid="bib20" ref-type="bibr">Lokugamage et al., 2020</xref>
), because of the protective effects of this interferon type in the respiratory tract. Subcutaneous IFNβ1a in combination with lopinavir/ritonavir is compared to lopinavir/ritonavir alone, hydroxychloroquine, and remdesivir in the DisCoVeRy trial (NCT04315948), which is the first clinical trial of the WHO Solidarity consortium of clinical trials.</p>
<p id="p0070">In conclusion, IFNβ1 may account for a safe and easy to upscale treatment against COVID-19 in the early stages of infection. Similar treatments had a mixed efficiency against MERS-CoV and SARS-CoV viruses, but <italic>in vitro</italic>
studies suggest that SARS-CoV-2 could be substantially more sensitive to IFN-I than other coronaviruses. The current lack of animal model for COVID-19 should not prevent the clinical evaluation of IFN-I treatment, since its safety has already been assessed in numerous independent clinical trials. Publications of data about IFN-based COVID-19 treatment performed in China in early 2020, expected in a near future, should give more accurate information on the relevance of this therapy.</p>
</sec>
<sec sec-type="COI-statement"><title>Declaration of competing interest</title>
<p id="p0075">None.</p>
</sec>
</body>
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<ack id="ACK0005"><title>Acknowledgments</title>
<p>The DisCoVeRy French Trial Management Committee includes the following members: Principal Investigator: Florence Ader. Scientific coordinator: Yazdan Yazdanpanah. Chief methodologist: France Mentre. Infectious diseases specialists: François-Xavier Lescure, Nathan Peiffer-Smadja. Intensivists: Lila Bouadma, Julien Poissy, Jean-François Timsit. Virologists: Bruno Lina, Florence Morfin-Sherpa. Pharmacologist: Gilles Peytavin. Genetic: Laurent Abel. Viral modeling: Jeremie Guedj. Clinical Trial Unit: Methodologists: Charles Burdet, Cedric Laouenan. Statisticians: Drifa Belhadi, Axelle Dupont. E-CRF designers and data managers: Basma Basli, Anissa Chair, Samira Laribi, Julie Level Marion Schneider, Marie-Capucine Tellier. Project manager: Aline Dechanet. INSERM sponsor: Sandrine Couffin-Cadiergues, Christelle Delmas, Hélène Esperou. Monitoring: Claire Fougerou, Ambre Gelley, Laëtitia Moinot, Linda Wittkop. ANRS coordination and Pharmacovigilance: Carole Cagnot, Alpha Diallo, Soizic Le Mestre, Delphine Lebrasseur-Longuet, Noemie Mercier, Ventzislava Petrov-Sanchez. Samples handling: Vinca Icard, Benjamin Leveau. Drug supply: Johanna Guillon, Anne-Marie Taburet. RENARCI: Marion Noret. REACTing: Eric D’ortenzio, Oriane Puechal, Juliette Saillard, Caroline Semaille.</p>
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