Beneficial effect of combinational methylprednisolone and remdesivir in hamster model of SARS-CoV-2 infection

Effective treatments for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Dexamethasone has been shown to confer survival benefits to certain groups of hospitalized patients, but whether glucocorticoids such as dexamethas...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Emerging microbes & infections 2021-01, Vol.10 (1), p.291-304
Hauptverfasser: Ye, Zi-Wei, Yuan, Shuofeng, Chan, Jasper Fuk-Woo, Zhang, Anna Jinxia, Yu, Ching-Yun, Ong, Chon Phin, Yang, Dong, Chan, Chris Chun-Yiu, Tang, Kaiming, Cao, Jianli, Poon, Vincent Kwok-Man, Chan, Chris Chung-Sing, Cai, Jian-Piao, Chu, Hin, Yuen, Kwok-Yung, Jin, Dong-Yan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 304
container_issue 1
container_start_page 291
container_title Emerging microbes & infections
container_volume 10
creator Ye, Zi-Wei
Yuan, Shuofeng
Chan, Jasper Fuk-Woo
Zhang, Anna Jinxia
Yu, Ching-Yun
Ong, Chon Phin
Yang, Dong
Chan, Chris Chun-Yiu
Tang, Kaiming
Cao, Jianli
Poon, Vincent Kwok-Man
Chan, Chris Chung-Sing
Cai, Jian-Piao
Chu, Hin
Yuen, Kwok-Yung
Jin, Dong-Yan
description Effective treatments for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Dexamethasone has been shown to confer survival benefits to certain groups of hospitalized patients, but whether glucocorticoids such as dexamethasone and methylprednisolone should be used together with antivirals to prevent a boost of SARS-CoV-2 replication remains to be determined. Here, we show the beneficial effect of methylprednisolone alone and in combination with remdesivir in the hamster model of SARS-CoV-2 infection. Treatment with methylprednisolone boosted RNA replication of SARS-CoV-2 but suppressed viral induction of proinflammatory cytokines in human monocyte-derived macrophages. Although methylprednisolone monotherapy alleviated body weight loss as well as nasal and pulmonary inflammation, viral loads increased and antibody response against the receptor-binding domain of spike protein attenuated. In contrast, a combination of methylprednisolone with remdesivir not only prevented body weight loss and inflammation, but also dampened viral protein expression and viral loads. In addition, the suppressive effect of methylprednisolone on antibody response was alleviated in the presence of remdesivir. Thus, combinational anti-inflammatory and antiviral therapy might be an effective, safer and more versatile treatment option for COVID-19. These data support testing of the efficacy of a combination of methylprednisolone and remdesivir for the treatment of COVID-19 in randomized controlled clinical trials.
doi_str_mv 10.1080/22221751.2021.1885998
format Article
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1080_22221751_2021_1885998</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_7b85688b98f94ddbba93c4479cc9dc95</doaj_id><sourcerecordid>33538646</sourcerecordid><originalsourceid>FETCH-LOGICAL-c534t-13063fa70cf231333901220fdf0163597749ede9bec9b2809ff5166e08d6f29d3</originalsourceid><addsrcrecordid>eNp9kd9KHTEQxhdpqWJ9hMq-wJ7mzyab3JTaQ2sFoVCrtyGbTDyRbHJItsp5-2Y9KnrTuUn4vpnfwHxN8wmjFUYCfSa18MDwiiCCV1gIJqU4aI4WvVuMd6_-h81JKXeo1oB4j_sPzSGljAre86Nm-gYRnDdehxacAzO3ybUmTaOPevYpVn2CebML2ww2-pJCitDqaNsMk4Xi731ufWw3eioz5HZKFsLCuDr7fdWt001Hqr2AK-xj897pUODk6T1urn98_7P-2V3-Or9Yn112htF-7jBFnDo9IOMIxZRSiTAhyFmHMKdMDkMvwYIcwciRCCSdY5hzQMJyR6Slx83FnmuTvlPb7Ceddypprx6FlG-VzrM3AdQwCsaFGKVwsrd2HLWkpu8HaYy0RrLK-rJnbf-OE1gDcc46vIG-daLfqNt0rwaJZU2mAtgeYHIqJYN7mcVILXGq5zjVEqd6irPOnb5e_DL1HF5t-LpvqPdNedIPKQerZr0LKbuso_FF0f_v-AcDh7Bq</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Beneficial effect of combinational methylprednisolone and remdesivir in hamster model of SARS-CoV-2 infection</title><source>Taylor &amp; Francis Open Access</source><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Ye, Zi-Wei ; Yuan, Shuofeng ; Chan, Jasper Fuk-Woo ; Zhang, Anna Jinxia ; Yu, Ching-Yun ; Ong, Chon Phin ; Yang, Dong ; Chan, Chris Chun-Yiu ; Tang, Kaiming ; Cao, Jianli ; Poon, Vincent Kwok-Man ; Chan, Chris Chung-Sing ; Cai, Jian-Piao ; Chu, Hin ; Yuen, Kwok-Yung ; Jin, Dong-Yan</creator><creatorcontrib>Ye, Zi-Wei ; Yuan, Shuofeng ; Chan, Jasper Fuk-Woo ; Zhang, Anna Jinxia ; Yu, Ching-Yun ; Ong, Chon Phin ; Yang, Dong ; Chan, Chris Chun-Yiu ; Tang, Kaiming ; Cao, Jianli ; Poon, Vincent Kwok-Man ; Chan, Chris Chung-Sing ; Cai, Jian-Piao ; Chu, Hin ; Yuen, Kwok-Yung ; Jin, Dong-Yan</creatorcontrib><description>Effective treatments for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Dexamethasone has been shown to confer survival benefits to certain groups of hospitalized patients, but whether glucocorticoids such as dexamethasone and methylprednisolone should be used together with antivirals to prevent a boost of SARS-CoV-2 replication remains to be determined. Here, we show the beneficial effect of methylprednisolone alone and in combination with remdesivir in the hamster model of SARS-CoV-2 infection. Treatment with methylprednisolone boosted RNA replication of SARS-CoV-2 but suppressed viral induction of proinflammatory cytokines in human monocyte-derived macrophages. Although methylprednisolone monotherapy alleviated body weight loss as well as nasal and pulmonary inflammation, viral loads increased and antibody response against the receptor-binding domain of spike protein attenuated. In contrast, a combination of methylprednisolone with remdesivir not only prevented body weight loss and inflammation, but also dampened viral protein expression and viral loads. In addition, the suppressive effect of methylprednisolone on antibody response was alleviated in the presence of remdesivir. Thus, combinational anti-inflammatory and antiviral therapy might be an effective, safer and more versatile treatment option for COVID-19. These data support testing of the efficacy of a combination of methylprednisolone and remdesivir for the treatment of COVID-19 in randomized controlled clinical trials.</description><identifier>ISSN: 2222-1751</identifier><identifier>EISSN: 2222-1751</identifier><identifier>DOI: 10.1080/22221751.2021.1885998</identifier><identifier>PMID: 33538646</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>Adenosine Monophosphate - analogs &amp; derivatives ; Adenosine Monophosphate - pharmacology ; Adenosine Monophosphate - therapeutic use ; Alanine - analogs &amp; derivatives ; Alanine - pharmacology ; Alanine - therapeutic use ; Animals ; Antibodies, Viral - blood ; Antiviral Agents - pharmacology ; Antiviral Agents - therapeutic use ; combination therapy ; Coronaviruses ; corticosteroid ; COVID-19 ; COVID-19 - drug therapy ; COVID-19 - pathology ; COVID-19 - virology ; Cytokines - biosynthesis ; Cytokines - immunology ; Disease Models, Animal ; Drug Therapy, Combination ; Female ; Humans ; Macrophages - immunology ; Macrophages - virology ; Male ; Mesocricetus ; Methylprednisolone - pharmacology ; Methylprednisolone - therapeutic use ; remdesivir ; Respiratory System - pathology ; Respiratory System - virology ; RNA, Viral ; SARS-CoV-2 ; SARS-CoV-2 - drug effects ; SARS-CoV-2 - physiology ; Spike Glycoprotein, Coronavirus - immunology ; Viral Load - drug effects ; Virus Replication - drug effects</subject><ispartof>Emerging microbes &amp; infections, 2021-01, Vol.10 (1), p.291-304</ispartof><rights>2021 The Author(s). Published by Informa UK Limited, trading as Taylor &amp; Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd 2021</rights><rights>2021 The Author(s). Published by Informa UK Limited, trading as Taylor &amp; Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd 2021 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c534t-13063fa70cf231333901220fdf0163597749ede9bec9b2809ff5166e08d6f29d3</citedby><cites>FETCH-LOGICAL-c534t-13063fa70cf231333901220fdf0163597749ede9bec9b2809ff5166e08d6f29d3</cites><orcidid>0000-0002-6446-4299 ; 0000-0001-6336-6657 ; 0000-0001-7996-1119 ; 0000-0002-2778-3530 ; 0000-0003-2855-9837 ; 0000-0002-2083-1552 ; 0000-0002-5087-3614 ; 0000-0001-6137-7926</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919885/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919885/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,27501,27923,27924,53790,53792,59142,59143</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33538646$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ye, Zi-Wei</creatorcontrib><creatorcontrib>Yuan, Shuofeng</creatorcontrib><creatorcontrib>Chan, Jasper Fuk-Woo</creatorcontrib><creatorcontrib>Zhang, Anna Jinxia</creatorcontrib><creatorcontrib>Yu, Ching-Yun</creatorcontrib><creatorcontrib>Ong, Chon Phin</creatorcontrib><creatorcontrib>Yang, Dong</creatorcontrib><creatorcontrib>Chan, Chris Chun-Yiu</creatorcontrib><creatorcontrib>Tang, Kaiming</creatorcontrib><creatorcontrib>Cao, Jianli</creatorcontrib><creatorcontrib>Poon, Vincent Kwok-Man</creatorcontrib><creatorcontrib>Chan, Chris Chung-Sing</creatorcontrib><creatorcontrib>Cai, Jian-Piao</creatorcontrib><creatorcontrib>Chu, Hin</creatorcontrib><creatorcontrib>Yuen, Kwok-Yung</creatorcontrib><creatorcontrib>Jin, Dong-Yan</creatorcontrib><title>Beneficial effect of combinational methylprednisolone and remdesivir in hamster model of SARS-CoV-2 infection</title><title>Emerging microbes &amp; infections</title><addtitle>Emerg Microbes Infect</addtitle><description>Effective treatments for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Dexamethasone has been shown to confer survival benefits to certain groups of hospitalized patients, but whether glucocorticoids such as dexamethasone and methylprednisolone should be used together with antivirals to prevent a boost of SARS-CoV-2 replication remains to be determined. Here, we show the beneficial effect of methylprednisolone alone and in combination with remdesivir in the hamster model of SARS-CoV-2 infection. Treatment with methylprednisolone boosted RNA replication of SARS-CoV-2 but suppressed viral induction of proinflammatory cytokines in human monocyte-derived macrophages. Although methylprednisolone monotherapy alleviated body weight loss as well as nasal and pulmonary inflammation, viral loads increased and antibody response against the receptor-binding domain of spike protein attenuated. In contrast, a combination of methylprednisolone with remdesivir not only prevented body weight loss and inflammation, but also dampened viral protein expression and viral loads. In addition, the suppressive effect of methylprednisolone on antibody response was alleviated in the presence of remdesivir. Thus, combinational anti-inflammatory and antiviral therapy might be an effective, safer and more versatile treatment option for COVID-19. These data support testing of the efficacy of a combination of methylprednisolone and remdesivir for the treatment of COVID-19 in randomized controlled clinical trials.</description><subject>Adenosine Monophosphate - analogs &amp; derivatives</subject><subject>Adenosine Monophosphate - pharmacology</subject><subject>Adenosine Monophosphate - therapeutic use</subject><subject>Alanine - analogs &amp; derivatives</subject><subject>Alanine - pharmacology</subject><subject>Alanine - therapeutic use</subject><subject>Animals</subject><subject>Antibodies, Viral - blood</subject><subject>Antiviral Agents - pharmacology</subject><subject>Antiviral Agents - therapeutic use</subject><subject>combination therapy</subject><subject>Coronaviruses</subject><subject>corticosteroid</subject><subject>COVID-19</subject><subject>COVID-19 - drug therapy</subject><subject>COVID-19 - pathology</subject><subject>COVID-19 - virology</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - immunology</subject><subject>Disease Models, Animal</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Humans</subject><subject>Macrophages - immunology</subject><subject>Macrophages - virology</subject><subject>Male</subject><subject>Mesocricetus</subject><subject>Methylprednisolone - pharmacology</subject><subject>Methylprednisolone - therapeutic use</subject><subject>remdesivir</subject><subject>Respiratory System - pathology</subject><subject>Respiratory System - virology</subject><subject>RNA, Viral</subject><subject>SARS-CoV-2</subject><subject>SARS-CoV-2 - drug effects</subject><subject>SARS-CoV-2 - physiology</subject><subject>Spike Glycoprotein, Coronavirus - immunology</subject><subject>Viral Load - drug effects</subject><subject>Virus Replication - drug effects</subject><issn>2222-1751</issn><issn>2222-1751</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNp9kd9KHTEQxhdpqWJ9hMq-wJ7mzyab3JTaQ2sFoVCrtyGbTDyRbHJItsp5-2Y9KnrTuUn4vpnfwHxN8wmjFUYCfSa18MDwiiCCV1gIJqU4aI4WvVuMd6_-h81JKXeo1oB4j_sPzSGljAre86Nm-gYRnDdehxacAzO3ybUmTaOPevYpVn2CebML2ww2-pJCitDqaNsMk4Xi731ufWw3eioz5HZKFsLCuDr7fdWt001Hqr2AK-xj897pUODk6T1urn98_7P-2V3-Or9Yn112htF-7jBFnDo9IOMIxZRSiTAhyFmHMKdMDkMvwYIcwciRCCSdY5hzQMJyR6Slx83FnmuTvlPb7Ceddypprx6FlG-VzrM3AdQwCsaFGKVwsrd2HLWkpu8HaYy0RrLK-rJnbf-OE1gDcc46vIG-daLfqNt0rwaJZU2mAtgeYHIqJYN7mcVILXGq5zjVEqd6irPOnb5e_DL1HF5t-LpvqPdNedIPKQerZr0LKbuso_FF0f_v-AcDh7Bq</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Ye, Zi-Wei</creator><creator>Yuan, Shuofeng</creator><creator>Chan, Jasper Fuk-Woo</creator><creator>Zhang, Anna Jinxia</creator><creator>Yu, Ching-Yun</creator><creator>Ong, Chon Phin</creator><creator>Yang, Dong</creator><creator>Chan, Chris Chun-Yiu</creator><creator>Tang, Kaiming</creator><creator>Cao, Jianli</creator><creator>Poon, Vincent Kwok-Man</creator><creator>Chan, Chris Chung-Sing</creator><creator>Cai, Jian-Piao</creator><creator>Chu, Hin</creator><creator>Yuen, Kwok-Yung</creator><creator>Jin, Dong-Yan</creator><general>Taylor &amp; Francis</general><general>Taylor &amp; Francis Group</general><scope>0YH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6446-4299</orcidid><orcidid>https://orcid.org/0000-0001-6336-6657</orcidid><orcidid>https://orcid.org/0000-0001-7996-1119</orcidid><orcidid>https://orcid.org/0000-0002-2778-3530</orcidid><orcidid>https://orcid.org/0000-0003-2855-9837</orcidid><orcidid>https://orcid.org/0000-0002-2083-1552</orcidid><orcidid>https://orcid.org/0000-0002-5087-3614</orcidid><orcidid>https://orcid.org/0000-0001-6137-7926</orcidid></search><sort><creationdate>20210101</creationdate><title>Beneficial effect of combinational methylprednisolone and remdesivir in hamster model of SARS-CoV-2 infection</title><author>Ye, Zi-Wei ; Yuan, Shuofeng ; Chan, Jasper Fuk-Woo ; Zhang, Anna Jinxia ; Yu, Ching-Yun ; Ong, Chon Phin ; Yang, Dong ; Chan, Chris Chun-Yiu ; Tang, Kaiming ; Cao, Jianli ; Poon, Vincent Kwok-Man ; Chan, Chris Chung-Sing ; Cai, Jian-Piao ; Chu, Hin ; Yuen, Kwok-Yung ; Jin, Dong-Yan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-13063fa70cf231333901220fdf0163597749ede9bec9b2809ff5166e08d6f29d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenosine Monophosphate - analogs &amp; derivatives</topic><topic>Adenosine Monophosphate - pharmacology</topic><topic>Adenosine Monophosphate - therapeutic use</topic><topic>Alanine - analogs &amp; derivatives</topic><topic>Alanine - pharmacology</topic><topic>Alanine - therapeutic use</topic><topic>Animals</topic><topic>Antibodies, Viral - blood</topic><topic>Antiviral Agents - pharmacology</topic><topic>Antiviral Agents - therapeutic use</topic><topic>combination therapy</topic><topic>Coronaviruses</topic><topic>corticosteroid</topic><topic>COVID-19</topic><topic>COVID-19 - drug therapy</topic><topic>COVID-19 - pathology</topic><topic>COVID-19 - virology</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - immunology</topic><topic>Disease Models, Animal</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Humans</topic><topic>Macrophages - immunology</topic><topic>Macrophages - virology</topic><topic>Male</topic><topic>Mesocricetus</topic><topic>Methylprednisolone - pharmacology</topic><topic>Methylprednisolone - therapeutic use</topic><topic>remdesivir</topic><topic>Respiratory System - pathology</topic><topic>Respiratory System - virology</topic><topic>RNA, Viral</topic><topic>SARS-CoV-2</topic><topic>SARS-CoV-2 - drug effects</topic><topic>SARS-CoV-2 - physiology</topic><topic>Spike Glycoprotein, Coronavirus - immunology</topic><topic>Viral Load - drug effects</topic><topic>Virus Replication - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ye, Zi-Wei</creatorcontrib><creatorcontrib>Yuan, Shuofeng</creatorcontrib><creatorcontrib>Chan, Jasper Fuk-Woo</creatorcontrib><creatorcontrib>Zhang, Anna Jinxia</creatorcontrib><creatorcontrib>Yu, Ching-Yun</creatorcontrib><creatorcontrib>Ong, Chon Phin</creatorcontrib><creatorcontrib>Yang, Dong</creatorcontrib><creatorcontrib>Chan, Chris Chun-Yiu</creatorcontrib><creatorcontrib>Tang, Kaiming</creatorcontrib><creatorcontrib>Cao, Jianli</creatorcontrib><creatorcontrib>Poon, Vincent Kwok-Man</creatorcontrib><creatorcontrib>Chan, Chris Chung-Sing</creatorcontrib><creatorcontrib>Cai, Jian-Piao</creatorcontrib><creatorcontrib>Chu, Hin</creatorcontrib><creatorcontrib>Yuen, Kwok-Yung</creatorcontrib><creatorcontrib>Jin, Dong-Yan</creatorcontrib><collection>Taylor &amp; Francis Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Emerging microbes &amp; infections</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ye, Zi-Wei</au><au>Yuan, Shuofeng</au><au>Chan, Jasper Fuk-Woo</au><au>Zhang, Anna Jinxia</au><au>Yu, Ching-Yun</au><au>Ong, Chon Phin</au><au>Yang, Dong</au><au>Chan, Chris Chun-Yiu</au><au>Tang, Kaiming</au><au>Cao, Jianli</au><au>Poon, Vincent Kwok-Man</au><au>Chan, Chris Chung-Sing</au><au>Cai, Jian-Piao</au><au>Chu, Hin</au><au>Yuen, Kwok-Yung</au><au>Jin, Dong-Yan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Beneficial effect of combinational methylprednisolone and remdesivir in hamster model of SARS-CoV-2 infection</atitle><jtitle>Emerging microbes &amp; infections</jtitle><addtitle>Emerg Microbes Infect</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>10</volume><issue>1</issue><spage>291</spage><epage>304</epage><pages>291-304</pages><issn>2222-1751</issn><eissn>2222-1751</eissn><abstract>Effective treatments for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Dexamethasone has been shown to confer survival benefits to certain groups of hospitalized patients, but whether glucocorticoids such as dexamethasone and methylprednisolone should be used together with antivirals to prevent a boost of SARS-CoV-2 replication remains to be determined. Here, we show the beneficial effect of methylprednisolone alone and in combination with remdesivir in the hamster model of SARS-CoV-2 infection. Treatment with methylprednisolone boosted RNA replication of SARS-CoV-2 but suppressed viral induction of proinflammatory cytokines in human monocyte-derived macrophages. Although methylprednisolone monotherapy alleviated body weight loss as well as nasal and pulmonary inflammation, viral loads increased and antibody response against the receptor-binding domain of spike protein attenuated. In contrast, a combination of methylprednisolone with remdesivir not only prevented body weight loss and inflammation, but also dampened viral protein expression and viral loads. In addition, the suppressive effect of methylprednisolone on antibody response was alleviated in the presence of remdesivir. Thus, combinational anti-inflammatory and antiviral therapy might be an effective, safer and more versatile treatment option for COVID-19. These data support testing of the efficacy of a combination of methylprednisolone and remdesivir for the treatment of COVID-19 in randomized controlled clinical trials.</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>33538646</pmid><doi>10.1080/22221751.2021.1885998</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-6446-4299</orcidid><orcidid>https://orcid.org/0000-0001-6336-6657</orcidid><orcidid>https://orcid.org/0000-0001-7996-1119</orcidid><orcidid>https://orcid.org/0000-0002-2778-3530</orcidid><orcidid>https://orcid.org/0000-0003-2855-9837</orcidid><orcidid>https://orcid.org/0000-0002-2083-1552</orcidid><orcidid>https://orcid.org/0000-0002-5087-3614</orcidid><orcidid>https://orcid.org/0000-0001-6137-7926</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2222-1751
ispartof Emerging microbes & infections, 2021-01, Vol.10 (1), p.291-304
issn 2222-1751
2222-1751
language eng
recordid cdi_crossref_primary_10_1080_22221751_2021_1885998
source Taylor & Francis Open Access; MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Adenosine Monophosphate - analogs & derivatives
Adenosine Monophosphate - pharmacology
Adenosine Monophosphate - therapeutic use
Alanine - analogs & derivatives
Alanine - pharmacology
Alanine - therapeutic use
Animals
Antibodies, Viral - blood
Antiviral Agents - pharmacology
Antiviral Agents - therapeutic use
combination therapy
Coronaviruses
corticosteroid
COVID-19
COVID-19 - drug therapy
COVID-19 - pathology
COVID-19 - virology
Cytokines - biosynthesis
Cytokines - immunology
Disease Models, Animal
Drug Therapy, Combination
Female
Humans
Macrophages - immunology
Macrophages - virology
Male
Mesocricetus
Methylprednisolone - pharmacology
Methylprednisolone - therapeutic use
remdesivir
Respiratory System - pathology
Respiratory System - virology
RNA, Viral
SARS-CoV-2
SARS-CoV-2 - drug effects
SARS-CoV-2 - physiology
Spike Glycoprotein, Coronavirus - immunology
Viral Load - drug effects
Virus Replication - drug effects
title Beneficial effect of combinational methylprednisolone and remdesivir in hamster model of SARS-CoV-2 infection
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T03%3A53%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Beneficial%20effect%20of%20combinational%20methylprednisolone%20and%20remdesivir%20in%20hamster%20model%20of%20SARS-CoV-2%20infection&rft.jtitle=Emerging%20microbes%20&%20infections&rft.au=Ye,%20Zi-Wei&rft.date=2021-01-01&rft.volume=10&rft.issue=1&rft.spage=291&rft.epage=304&rft.pages=291-304&rft.issn=2222-1751&rft.eissn=2222-1751&rft_id=info:doi/10.1080/22221751.2021.1885998&rft_dat=%3Cpubmed_cross%3E33538646%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/33538646&rft_doaj_id=oai_doaj_org_article_7b85688b98f94ddbba93c4479cc9dc95&rfr_iscdi=true