4.7 Article

Antibody cocktail effective against variants of SARS-CoV-2

Journal

JOURNAL OF BIOMEDICAL SCIENCE
Volume 28, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12929-021-00777-9

Keywords

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2); Receptor-binding domain (RBD); Neutralizing antibody; Cocktail therapy

Funding

  1. Academia Sinica, the Emerging Infectious and Major Disease Research Program [AS-KPQ-110-EIMD]
  2. Ministry of Science and Technology [MOST-108-3114-Y-001-002, MOST-108-2823-8-001-001, MOST 109-3114-Y-001-001]

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The study showed that six antibodies had varying binding and neutralizing abilities against SARS-CoV-2 variants, with antibody cocktails demonstrating potent neutralizing activities and potential therapeutic and prophylactic effects against multiple variants.
Background Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), an RNA virus with a high mutation rate. Importantly, several currently circulating SARS-CoV-2 variants are associated with loss of efficacy for both vaccines and neutralizing antibodies. Methods We analyzed the binding activity of six highly potent antibodies to the spike proteins of SARS-CoV-2 variants, assessed their neutralizing abilities with pseudovirus and authentic SARS-CoV-2 variants and evaluate efficacy of antibody cocktail in Delta SARS-CoV-2-infected hamster models as prophylactic and post-infection treatments. Results The tested RBD-chAbs, except RBD-chAb-25, maintained binding ability to spike proteins from SARS-CoV-2 variants. However, only RBD-chAb-45 and -51 retained neutralizing activities; RBD-chAb-1, -15, -25 and -28 exhibited diminished neutralization for all SARS-CoV-2 variants. Notably, several cocktails of our antibodies showed low IC50 values (3.35-27.06 ng/ml) against the SARS-CoV-2 variant pseudoviruses including United Kingdom variant B.1.1.7 (Alpha), South Africa variant B.1.351 (Beta), Brazil variant P1 (Gamma), California variant B.1.429 (Epsilon), New York variant B.1.526 (Iota), and India variants, B.1.617.1 (Kappa) and B.1.617.2 (Delta). RBD-chAb-45, and -51 showed PRNT50 values 4.93-37.54 ng/ml when used as single treatments or in combination with RBD-chAb-15 or -28, according to plaque assays with authentic Alpha, Gamma and Delta SARS-CoV-2 variants. Furthermore, the antibody cocktail of RBD-chAb-15 and -45 exhibited potent prophylactic and therapeutic effects in Delta SARS-CoV-2 variant-infected hamsters. Conclusions The cocktail of RBD-chAbs exhibited potent neutralizing activities against SARS-CoV-2 variants. These antibody cocktails are highly promising candidate tools for controlling new SARS-CoV-2 variants, including Delta.

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