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Human Monoclonal Antibody Cocktail for the Treatment or Prophylaxis of Middle East Respiratory Syndrome Coronavirus

BACKGROUND: REGN3048 and REGN3051 are human monoclonal antibodies (mAb) targeting the spike glycoprotein on the Middle East respiratory syndrome coronavirus (MERS-CoV), which binds to the receptor dipeptidyl peptidase-4 (DPP4) and is necessary for infection of susceptible cells. METHODS: Preclinical...

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Autores principales: Sivapalasingam, Sumathi, Saviolakis, George A, Kulcsar, Kirsten, Nakamura, Aya, Conrad, Thomas, Hassanein, Mohamed, Sumner, Giane, Elango, Chinnasamy, Kamal, Mohamed A, Eng, Simon, Kyratsous, Christos A, Musser, Bret J, Frieman, Matthew, Kantrowitz, Joel, Weinreich, David M, Yancopoulos, George, Stahl, Neil, Lipsich, Leah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7928873/
https://www.ncbi.nlm.nih.gov/pubmed/33507266
http://dx.doi.org/10.1093/infdis/jiab036
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author Sivapalasingam, Sumathi
Saviolakis, George A
Kulcsar, Kirsten
Nakamura, Aya
Conrad, Thomas
Hassanein, Mohamed
Sumner, Giane
Elango, Chinnasamy
Kamal, Mohamed A
Eng, Simon
Kyratsous, Christos A
Musser, Bret J
Frieman, Matthew
Kantrowitz, Joel
Weinreich, David M
Yancopoulos, George
Stahl, Neil
Lipsich, Leah
author_facet Sivapalasingam, Sumathi
Saviolakis, George A
Kulcsar, Kirsten
Nakamura, Aya
Conrad, Thomas
Hassanein, Mohamed
Sumner, Giane
Elango, Chinnasamy
Kamal, Mohamed A
Eng, Simon
Kyratsous, Christos A
Musser, Bret J
Frieman, Matthew
Kantrowitz, Joel
Weinreich, David M
Yancopoulos, George
Stahl, Neil
Lipsich, Leah
author_sort Sivapalasingam, Sumathi
collection PubMed
description BACKGROUND: REGN3048 and REGN3051 are human monoclonal antibodies (mAb) targeting the spike glycoprotein on the Middle East respiratory syndrome coronavirus (MERS-CoV), which binds to the receptor dipeptidyl peptidase-4 (DPP4) and is necessary for infection of susceptible cells. METHODS: Preclinical study: REGN3048, REGN3051 and isotype immunoglobulin G (IgG) were administered to humanized DPP4 (huDPP4) mice 1 day prior to and 1 day after infection with MERS-CoV (Jordan strain). Virus titers and lung pathology were assessed. Phase 1 study: healthy adults received the combined mAb (n = 36) or placebo (n = 12) and followed for 121 days. Six dose levels were studied. Strict safety criteria were met prior to dose escalation. RESULTS: Preclinical study: REGN3048 plus REGN3051, prophylactically or therapeutically, was substantially more effective for reducing viral titer, lung inflammation, and pathology in huDPP4 mice compared with control antibodies and to each antibody monotherapy. Phase 1 study: REGN3048 plus REGN3051 was well tolerated with no dose-limiting adverse events, deaths, serious adverse events, or infusion reactions. Each mAb displayed pharmacokinetics expected of human IgG1 antibodies; it was not immunogenic. CONCLUSIONS: REGN3048 and REGN3051 in combination were well tolerated. The clinical and preclinical data support further development for the treatment or prophylaxis of MERS-CoV infection.
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spelling pubmed-79288732021-03-04 Human Monoclonal Antibody Cocktail for the Treatment or Prophylaxis of Middle East Respiratory Syndrome Coronavirus Sivapalasingam, Sumathi Saviolakis, George A Kulcsar, Kirsten Nakamura, Aya Conrad, Thomas Hassanein, Mohamed Sumner, Giane Elango, Chinnasamy Kamal, Mohamed A Eng, Simon Kyratsous, Christos A Musser, Bret J Frieman, Matthew Kantrowitz, Joel Weinreich, David M Yancopoulos, George Stahl, Neil Lipsich, Leah J Infect Dis Major Articles and Brief Reports BACKGROUND: REGN3048 and REGN3051 are human monoclonal antibodies (mAb) targeting the spike glycoprotein on the Middle East respiratory syndrome coronavirus (MERS-CoV), which binds to the receptor dipeptidyl peptidase-4 (DPP4) and is necessary for infection of susceptible cells. METHODS: Preclinical study: REGN3048, REGN3051 and isotype immunoglobulin G (IgG) were administered to humanized DPP4 (huDPP4) mice 1 day prior to and 1 day after infection with MERS-CoV (Jordan strain). Virus titers and lung pathology were assessed. Phase 1 study: healthy adults received the combined mAb (n = 36) or placebo (n = 12) and followed for 121 days. Six dose levels were studied. Strict safety criteria were met prior to dose escalation. RESULTS: Preclinical study: REGN3048 plus REGN3051, prophylactically or therapeutically, was substantially more effective for reducing viral titer, lung inflammation, and pathology in huDPP4 mice compared with control antibodies and to each antibody monotherapy. Phase 1 study: REGN3048 plus REGN3051 was well tolerated with no dose-limiting adverse events, deaths, serious adverse events, or infusion reactions. Each mAb displayed pharmacokinetics expected of human IgG1 antibodies; it was not immunogenic. CONCLUSIONS: REGN3048 and REGN3051 in combination were well tolerated. The clinical and preclinical data support further development for the treatment or prophylaxis of MERS-CoV infection. Oxford University Press 2021-01-28 /pmc/articles/PMC7928873/ /pubmed/33507266 http://dx.doi.org/10.1093/infdis/jiab036 Text en © The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Articles and Brief Reports
Sivapalasingam, Sumathi
Saviolakis, George A
Kulcsar, Kirsten
Nakamura, Aya
Conrad, Thomas
Hassanein, Mohamed
Sumner, Giane
Elango, Chinnasamy
Kamal, Mohamed A
Eng, Simon
Kyratsous, Christos A
Musser, Bret J
Frieman, Matthew
Kantrowitz, Joel
Weinreich, David M
Yancopoulos, George
Stahl, Neil
Lipsich, Leah
Human Monoclonal Antibody Cocktail for the Treatment or Prophylaxis of Middle East Respiratory Syndrome Coronavirus
title Human Monoclonal Antibody Cocktail for the Treatment or Prophylaxis of Middle East Respiratory Syndrome Coronavirus
title_full Human Monoclonal Antibody Cocktail for the Treatment or Prophylaxis of Middle East Respiratory Syndrome Coronavirus
title_fullStr Human Monoclonal Antibody Cocktail for the Treatment or Prophylaxis of Middle East Respiratory Syndrome Coronavirus
title_full_unstemmed Human Monoclonal Antibody Cocktail for the Treatment or Prophylaxis of Middle East Respiratory Syndrome Coronavirus
title_short Human Monoclonal Antibody Cocktail for the Treatment or Prophylaxis of Middle East Respiratory Syndrome Coronavirus
title_sort human monoclonal antibody cocktail for the treatment or prophylaxis of middle east respiratory syndrome coronavirus
topic Major Articles and Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7928873/
https://www.ncbi.nlm.nih.gov/pubmed/33507266
http://dx.doi.org/10.1093/infdis/jiab036
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