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
Hauptverfasser: 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
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container_end_page 679
container_issue 3
container_start_page 671
container_title The Journal of infectious diseases
container_volume 229
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
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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 &lt; .001), and a steeper rate of decline through the first 5 days (P &lt; .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. 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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 &lt; .001), and a steeper rate of decline through the first 5 days (P &lt; .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 &amp; 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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 &lt; .001), and a steeper rate of decline through the first 5 days (P &lt; .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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ispartof The Journal of infectious diseases, 2024-03, Vol.229 (3), p.671-679
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1537-6613
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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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