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...
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Veröffentlicht in: | Emerging microbes & infections 2021-01, Vol.10 (1), p.291-304 |
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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 |
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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 & Francis</publisher><subject>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</subject><ispartof>Emerging microbes & infections, 2021-01, Vol.10 (1), p.291-304</ispartof><rights>2021 The Author(s). Published by Informa UK Limited, trading as Taylor & 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 & 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 & 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 & derivatives</subject><subject>Adenosine Monophosphate - pharmacology</subject><subject>Adenosine Monophosphate - therapeutic use</subject><subject>Alanine - analogs & 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 & Francis</general><general>Taylor & 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 & derivatives</topic><topic>Adenosine Monophosphate - pharmacology</topic><topic>Adenosine Monophosphate - therapeutic use</topic><topic>Alanine - analogs & 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 & 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 & 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 & 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. 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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 |
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