Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783659900989079552 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7928873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sivapalasingamsumathi humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT saviolakisgeorgea humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT kulcsarkirsten humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT nakamuraaya humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT conradthomas humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT hassaneinmohamed humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT sumnergiane humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT elangochinnasamy humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT kamalmohameda humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT engsimon humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT kyratsouschristosa humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT musserbretj humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT friemanmatthew humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT kantrowitzjoel humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT weinreichdavidm humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT yancopoulosgeorge humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT stahlneil humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus AT lipsichleah humanmonoclonalantibodycocktailforthetreatmentorprophylaxisofmiddleeastrespiratorysyndromecoronavirus |