Nasal delivery of single-domain antibody improves symptoms of SARS-CoV-2 infection in an animal model

PLoS Pathog. 2021 Oct 14;17(10):e1009542. doi: 10.1371/journal.ppat.1009542. eCollection 2021 Oct.

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes the disease COVID-19 can lead to serious symptoms, such as severe pneumonia, in the elderly and those with underlying medical conditions. While vaccines are now available, they do not work for everyone and therapeutic drugs are still needed, particularly for treating life-threatening conditions. Here, we showed nasal delivery of a new, unmodified camelid single-domain antibody (VHH), termed K-874A, effectively inhibited SARS-CoV-2 titers in infected lungs of Syrian hamsters without causing weight loss and cytokine induction. In vitro studies demonstrated that K-874A neutralized SARS-CoV-2 in both VeroE6/TMPRSS2 and human lung-derived alveolar organoid cells. Unlike other drug candidates, K-874A blocks viral membrane fusion rather than viral attachment. Cryo-electron microscopy revealed K-874A bound between the receptor binding domain and N-terminal domain of the virus S protein. Further, infected cells treated with K-874A produced fewer virus progeny that were less infective. We propose that direct administration of K-874A to the lung could be a new treatment for preventing the reinfection of amplified virus in COVID-19 patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Animals
  • Antibodies, Viral / administration & dosage*
  • Antiviral Agents / administration & dosage*
  • COVID-19*
  • Chlorocebus aethiops
  • Cricetinae
  • Disease Models, Animal
  • Humans
  • Mesocricetus
  • SARS-CoV-2
  • Single-Domain Antibodies / administration & dosage*
  • Spike Glycoprotein, Coronavirus / immunology
  • Vero Cells
  • Virus Attachment / drug effects*

Substances

  • Antibodies, Viral
  • Antiviral Agents
  • Single-Domain Antibodies
  • Spike Glycoprotein, Coronavirus

Grants and funding

This work is supported in part by the Japan Agency for Medical Research and Development (AMED) [20fk0108295s0101] (KK), Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)) from AMED [No. 2833] (KM) and the Kitasato project of COVID-19 Disease Control (KK).These funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This study was also supported by the Kitasato-Kao corp. collaboration research fund (KK), which had role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The Kitasato-Kao corp collaboration research fund (https://www.kao.com/global/en/worldwide/) The Kitasato Project of COVID-19 Disease Control (https://www.kitasato.ac.jp/jp/about/activities/covid-19/index.html).