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Monoclonal antibody treatment drives rapid culture conversion in SARS-CoV-2 infection

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) monoclonal antibodies (mAbs) are among the treatments recommended for high-risk ambulatory persons with coronavirus 2019 (COVID-19). Here, we study viral culture dynamics post-treatment in a subset of participants receiving the mAb bamlani...

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Autores principales: Boucau, Julie, Chew, Kara W., Choudhary, Manish C., Deo, Rinki, Regan, James, Flynn, James P., Crain, Charles R., Hughes, Michael D., Ritz, Justin, Moser, Carlee, Dragavon, Joan A., Javan, Arzhang C., Nirula, Ajay, Klekotka, Paul, Greninger, Alexander L., Coombs, Robert W., Fischer, William A., Daar, Eric S., Wohl, David A., Eron, Joseph J., Currier, Judith S., Smith, Davey M., Li, Jonathan Z., Barczak, Amy K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213028/
https://www.ncbi.nlm.nih.gov/pubmed/35793677
http://dx.doi.org/10.1016/j.xcrm.2022.100678
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author Boucau, Julie
Chew, Kara W.
Choudhary, Manish C.
Deo, Rinki
Regan, James
Flynn, James P.
Crain, Charles R.
Hughes, Michael D.
Ritz, Justin
Moser, Carlee
Dragavon, Joan A.
Javan, Arzhang C.
Nirula, Ajay
Klekotka, Paul
Greninger, Alexander L.
Coombs, Robert W.
Fischer, William A.
Daar, Eric S.
Wohl, David A.
Eron, Joseph J.
Currier, Judith S.
Smith, Davey M.
Li, Jonathan Z.
Barczak, Amy K.
author_facet Boucau, Julie
Chew, Kara W.
Choudhary, Manish C.
Deo, Rinki
Regan, James
Flynn, James P.
Crain, Charles R.
Hughes, Michael D.
Ritz, Justin
Moser, Carlee
Dragavon, Joan A.
Javan, Arzhang C.
Nirula, Ajay
Klekotka, Paul
Greninger, Alexander L.
Coombs, Robert W.
Fischer, William A.
Daar, Eric S.
Wohl, David A.
Eron, Joseph J.
Currier, Judith S.
Smith, Davey M.
Li, Jonathan Z.
Barczak, Amy K.
author_sort Boucau, Julie
collection PubMed
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) monoclonal antibodies (mAbs) are among the treatments recommended for high-risk ambulatory persons with coronavirus 2019 (COVID-19). Here, we study viral culture dynamics post-treatment in a subset of participants receiving the mAb bamlanivimab in the ACTIV-2 trial (ClinicalTrials.gov: NCT04518410). Viral load by qPCR and viral culture are performed from anterior nasal swabs collected on study days 0 (day of treatment), 1, 2, 3, and 7. Treatment with mAbs results in rapid clearance of culturable virus. One day after treatment, 0 of 28 (0%) participants receiving mAbs and 16 of 39 (41%) receiving placebo still have culturable virus (p < 0.0001). Recrudescence of culturable virus is detected in three participants with emerging mAb resistance and viral RNA rebound. While further studies are necessary to fully define the relationship between shed culturable virus and transmission, these results raise the possibility that mAbs may offer immediate (household) and public-health benefits by reducing onward transmission.
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spelling pubmed-92130282022-06-22 Monoclonal antibody treatment drives rapid culture conversion in SARS-CoV-2 infection Boucau, Julie Chew, Kara W. Choudhary, Manish C. Deo, Rinki Regan, James Flynn, James P. Crain, Charles R. Hughes, Michael D. Ritz, Justin Moser, Carlee Dragavon, Joan A. Javan, Arzhang C. Nirula, Ajay Klekotka, Paul Greninger, Alexander L. Coombs, Robert W. Fischer, William A. Daar, Eric S. Wohl, David A. Eron, Joseph J. Currier, Judith S. Smith, Davey M. Li, Jonathan Z. Barczak, Amy K. Cell Rep Med Report Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) monoclonal antibodies (mAbs) are among the treatments recommended for high-risk ambulatory persons with coronavirus 2019 (COVID-19). Here, we study viral culture dynamics post-treatment in a subset of participants receiving the mAb bamlanivimab in the ACTIV-2 trial (ClinicalTrials.gov: NCT04518410). Viral load by qPCR and viral culture are performed from anterior nasal swabs collected on study days 0 (day of treatment), 1, 2, 3, and 7. Treatment with mAbs results in rapid clearance of culturable virus. One day after treatment, 0 of 28 (0%) participants receiving mAbs and 16 of 39 (41%) receiving placebo still have culturable virus (p < 0.0001). Recrudescence of culturable virus is detected in three participants with emerging mAb resistance and viral RNA rebound. While further studies are necessary to fully define the relationship between shed culturable virus and transmission, these results raise the possibility that mAbs may offer immediate (household) and public-health benefits by reducing onward transmission. Elsevier 2022-06-20 /pmc/articles/PMC9213028/ /pubmed/35793677 http://dx.doi.org/10.1016/j.xcrm.2022.100678 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Report
Boucau, Julie
Chew, Kara W.
Choudhary, Manish C.
Deo, Rinki
Regan, James
Flynn, James P.
Crain, Charles R.
Hughes, Michael D.
Ritz, Justin
Moser, Carlee
Dragavon, Joan A.
Javan, Arzhang C.
Nirula, Ajay
Klekotka, Paul
Greninger, Alexander L.
Coombs, Robert W.
Fischer, William A.
Daar, Eric S.
Wohl, David A.
Eron, Joseph J.
Currier, Judith S.
Smith, Davey M.
Li, Jonathan Z.
Barczak, Amy K.
Monoclonal antibody treatment drives rapid culture conversion in SARS-CoV-2 infection
title Monoclonal antibody treatment drives rapid culture conversion in SARS-CoV-2 infection
title_full Monoclonal antibody treatment drives rapid culture conversion in SARS-CoV-2 infection
title_fullStr Monoclonal antibody treatment drives rapid culture conversion in SARS-CoV-2 infection
title_full_unstemmed Monoclonal antibody treatment drives rapid culture conversion in SARS-CoV-2 infection
title_short Monoclonal antibody treatment drives rapid culture conversion in SARS-CoV-2 infection
title_sort monoclonal antibody treatment drives rapid culture conversion in sars-cov-2 infection
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213028/
https://www.ncbi.nlm.nih.gov/pubmed/35793677
http://dx.doi.org/10.1016/j.xcrm.2022.100678
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