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Identification of Novel Neutralizing Monoclonal Antibodies against SARS-CoV-2 Spike Glycoprotein.
Bordoloi, Devivasha; Xu, Ziyang; Ho, Michelle; Purwar, Mansi; Bhojnagarwala, Pratik; Cassel, Joel; Giron, Leila B; Walker, Susanne; Kulkarni, Abhijeet J; Ruiz, Edgar Tello; Choi, Jihae; Zaidi, Faraz I; Wu, Yuanhan; Wang, Shaoying; Patel, Ami; Ramos, Stephanie; Smith, Trevor; Kulp, Daniel; Ugen, Kenneth E; Srinivasan, Alagarsamy; Abdel-Mohsen, Mohamed; Humeau, Laurent; Weiner, David B; Muthumani, Kar.
  • Bordoloi D; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Xu Z; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Ho M; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Purwar M; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Bhojnagarwala P; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Cassel J; Molecular Screening Facility, The Wistar Institute, Philadelphia, Pennsylvania 19104,United States.
  • Giron LB; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Walker S; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Kulkarni AJ; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Ruiz ET; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Choi J; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Zaidi FI; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Wu Y; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Wang S; Synbio Technologies, Monmouth Junction, New Jersey 08852, United States.
  • Patel A; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Ramos S; Inovio Pharmaceuticals, Plymouth Meeting, Pennsylvania 19462, United States.
  • Smith T; Inovio Pharmaceuticals, Plymouth Meeting, Pennsylvania 19462, United States.
  • Kulp D; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Ugen KE; Department of Molecular Medicine, University of South Florida Morsani College of Medicine, Tampa, Florida 33612, United States.
  • Srinivasan A; NanoBio Diagnostics, West Chester, Pennsylvania 19382, United States.
  • Abdel-Mohsen M; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Humeau L; Inovio Pharmaceuticals, Plymouth Meeting, Pennsylvania 19462, United States.
  • Weiner DB; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
  • Muthumani K; Vaccine & Immunotherapy Center, The Wistar Institute, Philadelphia, Pennsylvania 19104-4205, United States.
ACS Pharmacol Transl Sci ; 4(4): 1349-1361, 2021 Aug 13.
Article in English | MEDLINE | ID: covidwho-1358338
ABSTRACT
Coronavirus disease 2019 (COVID-19) is caused by the newly emerged human coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Due to the highly contagious nature of SARS-CoV-2, it has infected more than 137 million individuals and caused more than 2.9 million deaths globally as of April 13, 2021. There is an urgent need to develop effective novel therapeutic strategies to treat or prevent this infection. Toward this goal, we focused on the development of monoclonal antibodies (mAbs) directed against the SARS-CoV-2 spike glycoprotein (SARS-CoV-2 Spike) present on the surface of virus particles as well as virus-infected cells. We isolated anti-SARS-CoV-2 Spike mAbs from animals immunized with a DNA vaccine. We then selected a highly potent set of mAbs against SARS-CoV-2 Spike protein and evaluated each candidate for their expression, target binding affinity, and neutralization potential using complementary ACE2-blocking and pseudovirus neutralization assays. We identified a total of 10 antibodies, which specifically and strongly bound to SARS-CoV-2 Spike, blocked the receptor binding domain (RBD) and angiotensin-converting enzyme 2 (ACE2) interaction, and neutralized SARS-CoV-2. Furthermore, the glycomic profile of the antibodies suggested that they have high Fc-mediated effector functions. These antibodies should be further investigated for elucidating the neutralizing epitopes on Spike for the design of next-generation vaccines and for their potential in diagnostic as well as therapeutic utilities against SARS-CoV-2.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Topics: Vaccines Language: English Journal: ACS Pharmacol Transl Sci Year: 2021 Document Type: Article Affiliation country: Acsptsci.1c00058

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Topics: Vaccines Language: English Journal: ACS Pharmacol Transl Sci Year: 2021 Document Type: Article Affiliation country: Acsptsci.1c00058