Effect of Neutralizing Monoclonal Antibody Treatment on Early Trajectories of Virologic and Immunologic Biomarkers in Patients Hospitalized With COVID-19
Abstract Background Neutralizing monoclonal antibodies (nmAbs) failed to show clear benefit for hospitalized patients with coronavirus disease 2019 (COVID-19). Dynamics of virologic and immunologic biomarkers remain poorly understood. Methods Participants enrolled in the Therapeutics for Inpatients...
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Veröffentlicht in: | The Journal of infectious diseases 2024-03, Vol.229 (3), p.671-679 |
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creator | Jensen, Tomas O Grandits, Greg A Jain, Mamta K Murray, Thomas A Grund, Birgit Shaw-Saliba, Kathryn Matthay, Michael A Abassi, Mahsa Ardelt, Magdalena Baker, Jason V Chen, Peter Dewar, Robin L Goodman, Anna L Hatlen, Timothy J Highbarger, Helene C Holodniy, Mark Lallemand, Perrine Laverdure, Sylvain Leshnower, Bradley G Looney, David Moschopoulos, Charalampos D Mugerwa, Henry Murray, Daniel D Mylonakis, Eleftherios Nagy-Agren, Stephanie Rehman, M Tauseef Rupert, Adam Stevens, Randy A Turville, Stuart Weintrob, Amy Wick, Katherine Lundgren, Jens Ko, Emily R |
description | Abstract
Background
Neutralizing monoclonal antibodies (nmAbs) failed to show clear benefit for hospitalized patients with coronavirus disease 2019 (COVID-19). Dynamics of virologic and immunologic biomarkers remain poorly understood.
Methods
Participants enrolled in the Therapeutics for Inpatients with COVID-19 trials were randomized to nmAb versus placebo. Longitudinal differences between treatment and placebo groups in levels of plasma nucleocapsid antigen (N-Ag), anti-nucleocapsid antibody, C-reactive protein, interleukin-6, and D-dimer at enrollment, day 1, 3, and 5 were estimated using linear mixed models. A 7-point pulmonary ordinal scale assessed at day 5 was compared using proportional odds models.
Results
Analysis included 2149 participants enrolled between August 2020 and September 2021. Treatment resulted in 20% lower levels of plasma N-Ag compared with placebo (95% confidence interval, 12%–27%; P < .001), and a steeper rate of decline through the first 5 days (P < .001). The treatment difference did not vary between subgroups, and no difference was observed in trajectories of other biomarkers or the day 5 pulmonary ordinal scale.
Conclusions
Our study suggests that nmAb has an antiviral effect assessed by plasma N-Ag among hospitalized patients with COVID-19, with no blunting of the endogenous anti-nucleocapsid antibody response. No effect on systemic inflammation or day 5 clinical status was observed.
Clinical Trials Registration
NCT04501978.
Treatment with neutralizing monoclonal antibody lowered the trajectory of plasma nucleocapsid antigen over 5 days in patients hospitalized with COVID-19. No effect was seen on anti-nucleocapsid antibody, C-reactive protein, interleukin-6, D-dimer, or early clinical outcome by day 5. |
doi_str_mv | 10.1093/infdis/jiad446 |
format | Article |
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Background
Neutralizing monoclonal antibodies (nmAbs) failed to show clear benefit for hospitalized patients with coronavirus disease 2019 (COVID-19). Dynamics of virologic and immunologic biomarkers remain poorly understood.
Methods
Participants enrolled in the Therapeutics for Inpatients with COVID-19 trials were randomized to nmAb versus placebo. Longitudinal differences between treatment and placebo groups in levels of plasma nucleocapsid antigen (N-Ag), anti-nucleocapsid antibody, C-reactive protein, interleukin-6, and D-dimer at enrollment, day 1, 3, and 5 were estimated using linear mixed models. A 7-point pulmonary ordinal scale assessed at day 5 was compared using proportional odds models.
Results
Analysis included 2149 participants enrolled between August 2020 and September 2021. Treatment resulted in 20% lower levels of plasma N-Ag compared with placebo (95% confidence interval, 12%–27%; P < .001), and a steeper rate of decline through the first 5 days (P < .001). The treatment difference did not vary between subgroups, and no difference was observed in trajectories of other biomarkers or the day 5 pulmonary ordinal scale.
Conclusions
Our study suggests that nmAb has an antiviral effect assessed by plasma N-Ag among hospitalized patients with COVID-19, with no blunting of the endogenous anti-nucleocapsid antibody response. No effect on systemic inflammation or day 5 clinical status was observed.
Clinical Trials Registration
NCT04501978.
Treatment with neutralizing monoclonal antibody lowered the trajectory of plasma nucleocapsid antigen over 5 days in patients hospitalized with COVID-19. No effect was seen on anti-nucleocapsid antibody, C-reactive protein, interleukin-6, D-dimer, or early clinical outcome by day 5.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiad446</identifier><identifier>PMID: 37948759</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Antibodies ; Antibodies, Monoclonal - therapeutic use ; Antibodies, Neutralizing ; Antibody response ; Biomarkers ; C-reactive protein ; Clinical trials ; Coronaviruses ; COVID-19 ; Hospitalization ; Humans ; Interleukin 6 ; Major ; Monoclonal antibodies ; Nucleocapsids ; Patients ; Placebos ; SARS-CoV-2</subject><ispartof>The Journal of infectious diseases, 2024-03, Vol.229 (3), p.671-679</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2023</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c408t-49b7baff377d45ab046671cd14bb785f1df5ee7ee7529428c99458b18fe6a3183</cites><orcidid>0000-0001-8901-7850 ; 0000-0003-0398-4431 ; 0000-0003-2292-6544 ; 0000-0001-9601-3006 ; 0000-0002-6655-7982 ; 0000-0002-4624-0777</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37948759$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jensen, Tomas O</creatorcontrib><creatorcontrib>Grandits, Greg A</creatorcontrib><creatorcontrib>Jain, Mamta K</creatorcontrib><creatorcontrib>Murray, Thomas A</creatorcontrib><creatorcontrib>Grund, Birgit</creatorcontrib><creatorcontrib>Shaw-Saliba, Kathryn</creatorcontrib><creatorcontrib>Matthay, Michael A</creatorcontrib><creatorcontrib>Abassi, Mahsa</creatorcontrib><creatorcontrib>Ardelt, Magdalena</creatorcontrib><creatorcontrib>Baker, Jason V</creatorcontrib><creatorcontrib>Chen, Peter</creatorcontrib><creatorcontrib>Dewar, Robin L</creatorcontrib><creatorcontrib>Goodman, Anna L</creatorcontrib><creatorcontrib>Hatlen, Timothy J</creatorcontrib><creatorcontrib>Highbarger, Helene C</creatorcontrib><creatorcontrib>Holodniy, Mark</creatorcontrib><creatorcontrib>Lallemand, Perrine</creatorcontrib><creatorcontrib>Laverdure, Sylvain</creatorcontrib><creatorcontrib>Leshnower, Bradley G</creatorcontrib><creatorcontrib>Looney, David</creatorcontrib><creatorcontrib>Moschopoulos, Charalampos D</creatorcontrib><creatorcontrib>Mugerwa, Henry</creatorcontrib><creatorcontrib>Murray, Daniel D</creatorcontrib><creatorcontrib>Mylonakis, Eleftherios</creatorcontrib><creatorcontrib>Nagy-Agren, Stephanie</creatorcontrib><creatorcontrib>Rehman, M Tauseef</creatorcontrib><creatorcontrib>Rupert, Adam</creatorcontrib><creatorcontrib>Stevens, Randy A</creatorcontrib><creatorcontrib>Turville, Stuart</creatorcontrib><creatorcontrib>Weintrob, Amy</creatorcontrib><creatorcontrib>Wick, Katherine</creatorcontrib><creatorcontrib>Lundgren, Jens</creatorcontrib><creatorcontrib>Ko, Emily R</creatorcontrib><creatorcontrib>ACTIV-3/TICO Study Group</creatorcontrib><creatorcontrib>for the ACTIV-3/TICO Study Group</creatorcontrib><title>Effect of Neutralizing Monoclonal Antibody Treatment on Early Trajectories of Virologic and Immunologic Biomarkers in Patients Hospitalized With COVID-19</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Abstract
Background
Neutralizing monoclonal antibodies (nmAbs) failed to show clear benefit for hospitalized patients with coronavirus disease 2019 (COVID-19). Dynamics of virologic and immunologic biomarkers remain poorly understood.
Methods
Participants enrolled in the Therapeutics for Inpatients with COVID-19 trials were randomized to nmAb versus placebo. Longitudinal differences between treatment and placebo groups in levels of plasma nucleocapsid antigen (N-Ag), anti-nucleocapsid antibody, C-reactive protein, interleukin-6, and D-dimer at enrollment, day 1, 3, and 5 were estimated using linear mixed models. A 7-point pulmonary ordinal scale assessed at day 5 was compared using proportional odds models.
Results
Analysis included 2149 participants enrolled between August 2020 and September 2021. Treatment resulted in 20% lower levels of plasma N-Ag compared with placebo (95% confidence interval, 12%–27%; P < .001), and a steeper rate of decline through the first 5 days (P < .001). The treatment difference did not vary between subgroups, and no difference was observed in trajectories of other biomarkers or the day 5 pulmonary ordinal scale.
Conclusions
Our study suggests that nmAb has an antiviral effect assessed by plasma N-Ag among hospitalized patients with COVID-19, with no blunting of the endogenous anti-nucleocapsid antibody response. No effect on systemic inflammation or day 5 clinical status was observed.
Clinical Trials Registration
NCT04501978.
Treatment with neutralizing monoclonal antibody lowered the trajectory of plasma nucleocapsid antigen over 5 days in patients hospitalized with COVID-19. No effect was seen on anti-nucleocapsid antibody, C-reactive protein, interleukin-6, D-dimer, or early clinical outcome by day 5.</description><subject>Antibodies</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antibodies, Neutralizing</subject><subject>Antibody response</subject><subject>Biomarkers</subject><subject>C-reactive protein</subject><subject>Clinical trials</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Interleukin 6</subject><subject>Major</subject><subject>Monoclonal antibodies</subject><subject>Nucleocapsids</subject><subject>Patients</subject><subject>Placebos</subject><subject>SARS-CoV-2</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNqFkUFvFCEYhomxsWv16tGQeNHDtDDAACdT19Vu0loPtR4JM8CWdQZWmDGp_8R_K9vdNurFhIQAz_d-L-8HwAuMjjGS5MQHZ3w-WXttKG0egRlmhFdNg8ljMEOorisspDwET3NeI4QoafgTcEi4pIIzOQO_Fs7ZboTRwU92GpPu_U8fVvAihtj1MegenobRt9Hcwqtk9TjYUOgAFzr12yu9LuUxeZu3Gtc-xT6ufAd1MHA5DFPYn9_5OOj0zaYMfYCf9eiLUIZnMW_8uO1qDfzqxxs4v7xevq-wfAYOnO6zfb7fj8CXD4ur-Vl1fvlxOT89rzqKxFhR2fJWO0c4N5TpFtGm4bgzmLYtF8xh45i1vCxWS1qLTkrKRIuFs40mWJAj8Hanu5nawZqu2CopqE3yxe-titqrv1-Cv1Gr-ENt8xc1qovC671Cit8nm0c1-NzZvtfBximrWghZU4KYLOirf9B1nFJJOSuCG0brRjJSqOMd1aWYc7LuwQ1Gd23VbuxqP_ZS8PLPPzzg93MuwJsdEKfN_8R-AxzgvGw</recordid><startdate>20240314</startdate><enddate>20240314</enddate><creator>Jensen, Tomas O</creator><creator>Grandits, Greg A</creator><creator>Jain, Mamta K</creator><creator>Murray, Thomas A</creator><creator>Grund, Birgit</creator><creator>Shaw-Saliba, Kathryn</creator><creator>Matthay, Michael A</creator><creator>Abassi, Mahsa</creator><creator>Ardelt, Magdalena</creator><creator>Baker, Jason V</creator><creator>Chen, Peter</creator><creator>Dewar, Robin L</creator><creator>Goodman, Anna L</creator><creator>Hatlen, Timothy J</creator><creator>Highbarger, Helene C</creator><creator>Holodniy, Mark</creator><creator>Lallemand, Perrine</creator><creator>Laverdure, Sylvain</creator><creator>Leshnower, Bradley G</creator><creator>Looney, David</creator><creator>Moschopoulos, Charalampos D</creator><creator>Mugerwa, Henry</creator><creator>Murray, Daniel D</creator><creator>Mylonakis, Eleftherios</creator><creator>Nagy-Agren, Stephanie</creator><creator>Rehman, M Tauseef</creator><creator>Rupert, Adam</creator><creator>Stevens, Randy A</creator><creator>Turville, Stuart</creator><creator>Weintrob, Amy</creator><creator>Wick, Katherine</creator><creator>Lundgren, Jens</creator><creator>Ko, Emily R</creator><general>Oxford University Press</general><scope>TOX</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>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8901-7850</orcidid><orcidid>https://orcid.org/0000-0003-0398-4431</orcidid><orcidid>https://orcid.org/0000-0003-2292-6544</orcidid><orcidid>https://orcid.org/0000-0001-9601-3006</orcidid><orcidid>https://orcid.org/0000-0002-6655-7982</orcidid><orcidid>https://orcid.org/0000-0002-4624-0777</orcidid></search><sort><creationdate>20240314</creationdate><title>Effect of Neutralizing Monoclonal Antibody Treatment on Early Trajectories of Virologic and Immunologic Biomarkers in Patients Hospitalized With COVID-19</title><author>Jensen, Tomas O ; Grandits, Greg A ; Jain, Mamta K ; Murray, Thomas A ; Grund, Birgit ; Shaw-Saliba, Kathryn ; Matthay, Michael A ; Abassi, Mahsa ; Ardelt, Magdalena ; Baker, Jason V ; Chen, Peter ; Dewar, Robin L ; Goodman, Anna L ; Hatlen, Timothy J ; Highbarger, Helene C ; Holodniy, Mark ; Lallemand, Perrine ; Laverdure, Sylvain ; Leshnower, Bradley G ; Looney, David ; Moschopoulos, Charalampos D ; Mugerwa, Henry ; Murray, Daniel D ; Mylonakis, Eleftherios ; Nagy-Agren, Stephanie ; Rehman, M Tauseef ; Rupert, Adam ; Stevens, Randy A ; Turville, Stuart ; Weintrob, Amy ; Wick, Katherine ; Lundgren, Jens ; Ko, Emily R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-49b7baff377d45ab046671cd14bb785f1df5ee7ee7529428c99458b18fe6a3183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antibodies</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Antibodies, Neutralizing</topic><topic>Antibody response</topic><topic>Biomarkers</topic><topic>C-reactive protein</topic><topic>Clinical trials</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>Interleukin 6</topic><topic>Major</topic><topic>Monoclonal antibodies</topic><topic>Nucleocapsids</topic><topic>Patients</topic><topic>Placebos</topic><topic>SARS-CoV-2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jensen, Tomas O</creatorcontrib><creatorcontrib>Grandits, Greg A</creatorcontrib><creatorcontrib>Jain, Mamta K</creatorcontrib><creatorcontrib>Murray, Thomas A</creatorcontrib><creatorcontrib>Grund, Birgit</creatorcontrib><creatorcontrib>Shaw-Saliba, Kathryn</creatorcontrib><creatorcontrib>Matthay, Michael A</creatorcontrib><creatorcontrib>Abassi, Mahsa</creatorcontrib><creatorcontrib>Ardelt, Magdalena</creatorcontrib><creatorcontrib>Baker, Jason V</creatorcontrib><creatorcontrib>Chen, Peter</creatorcontrib><creatorcontrib>Dewar, Robin L</creatorcontrib><creatorcontrib>Goodman, Anna L</creatorcontrib><creatorcontrib>Hatlen, Timothy J</creatorcontrib><creatorcontrib>Highbarger, Helene C</creatorcontrib><creatorcontrib>Holodniy, Mark</creatorcontrib><creatorcontrib>Lallemand, Perrine</creatorcontrib><creatorcontrib>Laverdure, Sylvain</creatorcontrib><creatorcontrib>Leshnower, Bradley G</creatorcontrib><creatorcontrib>Looney, David</creatorcontrib><creatorcontrib>Moschopoulos, Charalampos D</creatorcontrib><creatorcontrib>Mugerwa, Henry</creatorcontrib><creatorcontrib>Murray, Daniel D</creatorcontrib><creatorcontrib>Mylonakis, Eleftherios</creatorcontrib><creatorcontrib>Nagy-Agren, Stephanie</creatorcontrib><creatorcontrib>Rehman, M Tauseef</creatorcontrib><creatorcontrib>Rupert, Adam</creatorcontrib><creatorcontrib>Stevens, Randy A</creatorcontrib><creatorcontrib>Turville, Stuart</creatorcontrib><creatorcontrib>Weintrob, Amy</creatorcontrib><creatorcontrib>Wick, Katherine</creatorcontrib><creatorcontrib>Lundgren, Jens</creatorcontrib><creatorcontrib>Ko, Emily R</creatorcontrib><creatorcontrib>ACTIV-3/TICO Study Group</creatorcontrib><creatorcontrib>for the ACTIV-3/TICO Study Group</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jensen, Tomas O</au><au>Grandits, Greg A</au><au>Jain, Mamta K</au><au>Murray, Thomas A</au><au>Grund, Birgit</au><au>Shaw-Saliba, Kathryn</au><au>Matthay, Michael A</au><au>Abassi, Mahsa</au><au>Ardelt, Magdalena</au><au>Baker, Jason V</au><au>Chen, Peter</au><au>Dewar, Robin L</au><au>Goodman, Anna L</au><au>Hatlen, Timothy J</au><au>Highbarger, Helene C</au><au>Holodniy, Mark</au><au>Lallemand, Perrine</au><au>Laverdure, Sylvain</au><au>Leshnower, Bradley G</au><au>Looney, David</au><au>Moschopoulos, Charalampos D</au><au>Mugerwa, Henry</au><au>Murray, Daniel D</au><au>Mylonakis, Eleftherios</au><au>Nagy-Agren, Stephanie</au><au>Rehman, M Tauseef</au><au>Rupert, Adam</au><au>Stevens, Randy A</au><au>Turville, Stuart</au><au>Weintrob, Amy</au><au>Wick, Katherine</au><au>Lundgren, Jens</au><au>Ko, Emily R</au><aucorp>ACTIV-3/TICO Study Group</aucorp><aucorp>for the ACTIV-3/TICO Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Neutralizing Monoclonal Antibody Treatment on Early Trajectories of Virologic and Immunologic Biomarkers in Patients Hospitalized With COVID-19</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2024-03-14</date><risdate>2024</risdate><volume>229</volume><issue>3</issue><spage>671</spage><epage>679</epage><pages>671-679</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>Abstract
Background
Neutralizing monoclonal antibodies (nmAbs) failed to show clear benefit for hospitalized patients with coronavirus disease 2019 (COVID-19). Dynamics of virologic and immunologic biomarkers remain poorly understood.
Methods
Participants enrolled in the Therapeutics for Inpatients with COVID-19 trials were randomized to nmAb versus placebo. Longitudinal differences between treatment and placebo groups in levels of plasma nucleocapsid antigen (N-Ag), anti-nucleocapsid antibody, C-reactive protein, interleukin-6, and D-dimer at enrollment, day 1, 3, and 5 were estimated using linear mixed models. A 7-point pulmonary ordinal scale assessed at day 5 was compared using proportional odds models.
Results
Analysis included 2149 participants enrolled between August 2020 and September 2021. Treatment resulted in 20% lower levels of plasma N-Ag compared with placebo (95% confidence interval, 12%–27%; P < .001), and a steeper rate of decline through the first 5 days (P < .001). The treatment difference did not vary between subgroups, and no difference was observed in trajectories of other biomarkers or the day 5 pulmonary ordinal scale.
Conclusions
Our study suggests that nmAb has an antiviral effect assessed by plasma N-Ag among hospitalized patients with COVID-19, with no blunting of the endogenous anti-nucleocapsid antibody response. No effect on systemic inflammation or day 5 clinical status was observed.
Clinical Trials Registration
NCT04501978.
Treatment with neutralizing monoclonal antibody lowered the trajectory of plasma nucleocapsid antigen over 5 days in patients hospitalized with COVID-19. No effect was seen on anti-nucleocapsid antibody, C-reactive protein, interleukin-6, D-dimer, or early clinical outcome by day 5.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>37948759</pmid><doi>10.1093/infdis/jiad446</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8901-7850</orcidid><orcidid>https://orcid.org/0000-0003-0398-4431</orcidid><orcidid>https://orcid.org/0000-0003-2292-6544</orcidid><orcidid>https://orcid.org/0000-0001-9601-3006</orcidid><orcidid>https://orcid.org/0000-0002-6655-7982</orcidid><orcidid>https://orcid.org/0000-0002-4624-0777</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE |
subjects | Antibodies Antibodies, Monoclonal - therapeutic use Antibodies, Neutralizing Antibody response Biomarkers C-reactive protein Clinical trials Coronaviruses COVID-19 Hospitalization Humans Interleukin 6 Major Monoclonal antibodies Nucleocapsids Patients Placebos SARS-CoV-2 |
title | Effect of Neutralizing Monoclonal Antibody Treatment on Early Trajectories of Virologic and Immunologic Biomarkers in Patients Hospitalized With COVID-19 |
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