H1N1 nanobody development and therapeutic efficacy verification in H1N1-challenged mice
- PMID: 38805966
- DOI: 10.1016/j.biopha.2024.116781
H1N1 nanobody development and therapeutic efficacy verification in H1N1-challenged mice
Erratum in
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Corrigendum to "H1N1 nanobody development and therapeutic efficacy verification in H1N1-challenged mice" [Biomed. Pharmacother. 176 (2024) 116781].Biomed Pharmacother. 2025 Jul;188:118212. doi: 10.1016/j.biopha.2025.118212. Epub 2025 May 30. Biomed Pharmacother. 2025. PMID: 40450463 No abstract available.
Abstract
Influenza A virus causes numerous deaths and infections worldwide annually. Therefore, we have considered nanobodies as a potential treatment for patients with severe cases of influenza. We developed a nanobody that was expected to have protective efficacy against the A/California/04/2009 (CA/04; pandemic 2009 flu strain) and evaluated its therapeutic efficacy against CA/04 in mice experiments. This nanobody was derived from the immunization of the alpaca, and the inactivated CA/04 virus was used as an immunogen. We successfully generated a nanobody library through bio-panning, phage ELISA, and Bio-layer interferometry. Moreover, we confirmed that administering nanobodies after lethal doses of CA/04 reduced viral replication in the lungs and influenza-induced clinical signs in mice. These research findings will help to develop nanobodies as viral therapeutics for CA/04 and other infectious viruses.
Keywords: Influenza; Mice experiment; Nanobody; Pandemic 2009 flu; Viral therapeutic.
Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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