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New Anti-Flavivirus Fusion Loop Human Antibodies with Zika Virus-Neutralizing Potential

Zika virus infections exhibit recurrent outbreaks and can be responsible for disease complications such as congenital Zika virus syndrome. Effective therapeutic interventions are still a challenge. Antibodies can provide significant protection, although the antibody response may fail due to antibody...

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Autores principales: França, Renato Kaylan Alves de Oliveira, Silva, Jacyelle Medeiros, Rodrigues, Lucas Silva, Sokolowskei, Dimitri, Brigido, Marcelo Macedo, Maranhão, Andrea Queiroz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321016/
https://www.ncbi.nlm.nih.gov/pubmed/35887153
http://dx.doi.org/10.3390/ijms23147805
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author França, Renato Kaylan Alves de Oliveira
Silva, Jacyelle Medeiros
Rodrigues, Lucas Silva
Sokolowskei, Dimitri
Brigido, Marcelo Macedo
Maranhão, Andrea Queiroz
author_facet França, Renato Kaylan Alves de Oliveira
Silva, Jacyelle Medeiros
Rodrigues, Lucas Silva
Sokolowskei, Dimitri
Brigido, Marcelo Macedo
Maranhão, Andrea Queiroz
author_sort França, Renato Kaylan Alves de Oliveira
collection PubMed
description Zika virus infections exhibit recurrent outbreaks and can be responsible for disease complications such as congenital Zika virus syndrome. Effective therapeutic interventions are still a challenge. Antibodies can provide significant protection, although the antibody response may fail due to antibody-dependent enhancement reactions. The choice of the target antigen is a crucial part of the process to generate effective neutralizing antibodies. Human anti-Zika virus antibodies were selected by phage display technology. The antibodies were selected against a mimetic peptide based on the fusion loop region in the protein E of Zika virus, which is highly conserved among different flaviviruses. Four rounds of selection were performed using the synthetic peptide in two strategies: the first was using the acidic elution of bound phages, and the second was by applying a competing procedure. After panning, the selected VH and VL domains were determined by combining NGS and bioinformatic approaches. Three different human monoclonal antibodies were expressed as scFvs and further characterized. All showed a binding capacity to Zika (ZIKV) and showed cross-recognition with yellow fever (YFV) and dengue (DENV) viruses. Two of these antibodies, AZ1p and AZ6m, could neutralize the ZIKV infection in vitro. Due to the conservation of the fusion loop region, these new antibodies can potentially be used in therapeutic intervention against Zika virus and other flavivirus illnesses.
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spelling pubmed-93210162022-07-27 New Anti-Flavivirus Fusion Loop Human Antibodies with Zika Virus-Neutralizing Potential França, Renato Kaylan Alves de Oliveira Silva, Jacyelle Medeiros Rodrigues, Lucas Silva Sokolowskei, Dimitri Brigido, Marcelo Macedo Maranhão, Andrea Queiroz Int J Mol Sci Article Zika virus infections exhibit recurrent outbreaks and can be responsible for disease complications such as congenital Zika virus syndrome. Effective therapeutic interventions are still a challenge. Antibodies can provide significant protection, although the antibody response may fail due to antibody-dependent enhancement reactions. The choice of the target antigen is a crucial part of the process to generate effective neutralizing antibodies. Human anti-Zika virus antibodies were selected by phage display technology. The antibodies were selected against a mimetic peptide based on the fusion loop region in the protein E of Zika virus, which is highly conserved among different flaviviruses. Four rounds of selection were performed using the synthetic peptide in two strategies: the first was using the acidic elution of bound phages, and the second was by applying a competing procedure. After panning, the selected VH and VL domains were determined by combining NGS and bioinformatic approaches. Three different human monoclonal antibodies were expressed as scFvs and further characterized. All showed a binding capacity to Zika (ZIKV) and showed cross-recognition with yellow fever (YFV) and dengue (DENV) viruses. Two of these antibodies, AZ1p and AZ6m, could neutralize the ZIKV infection in vitro. Due to the conservation of the fusion loop region, these new antibodies can potentially be used in therapeutic intervention against Zika virus and other flavivirus illnesses. MDPI 2022-07-15 /pmc/articles/PMC9321016/ /pubmed/35887153 http://dx.doi.org/10.3390/ijms23147805 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
França, Renato Kaylan Alves de Oliveira
Silva, Jacyelle Medeiros
Rodrigues, Lucas Silva
Sokolowskei, Dimitri
Brigido, Marcelo Macedo
Maranhão, Andrea Queiroz
New Anti-Flavivirus Fusion Loop Human Antibodies with Zika Virus-Neutralizing Potential
title New Anti-Flavivirus Fusion Loop Human Antibodies with Zika Virus-Neutralizing Potential
title_full New Anti-Flavivirus Fusion Loop Human Antibodies with Zika Virus-Neutralizing Potential
title_fullStr New Anti-Flavivirus Fusion Loop Human Antibodies with Zika Virus-Neutralizing Potential
title_full_unstemmed New Anti-Flavivirus Fusion Loop Human Antibodies with Zika Virus-Neutralizing Potential
title_short New Anti-Flavivirus Fusion Loop Human Antibodies with Zika Virus-Neutralizing Potential
title_sort new anti-flavivirus fusion loop human antibodies with zika virus-neutralizing potential
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321016/
https://www.ncbi.nlm.nih.gov/pubmed/35887153
http://dx.doi.org/10.3390/ijms23147805
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