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Generation of “OP7 chimera” defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice
Influenza A virus (IAV) defective interfering particles (DIPs) are considered as new promising antiviral agents. Conventional DIPs (cDIPs) contain a deletion in the genome and can only replicate upon co-infection with infectious standard virus (STV), during which they suppress STV replication. We pr...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684881/ https://www.ncbi.nlm.nih.gov/pubmed/38017026 http://dx.doi.org/10.1038/s41598-023-47547-1 |
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author | Dogra, Tanya Pelz, Lars Boehme, Julia D. Kuechler, Jan Kershaw, Olivia Marichal-Gallardo, Pavel Baelkner, Maike Hein, Marc D. Gruber, Achim D. Benndorf, Dirk Genzel, Yvonne Bruder, Dunja Kupke, Sascha Y. Reichl, Udo |
author_facet | Dogra, Tanya Pelz, Lars Boehme, Julia D. Kuechler, Jan Kershaw, Olivia Marichal-Gallardo, Pavel Baelkner, Maike Hein, Marc D. Gruber, Achim D. Benndorf, Dirk Genzel, Yvonne Bruder, Dunja Kupke, Sascha Y. Reichl, Udo |
author_sort | Dogra, Tanya |
collection | PubMed |
description | Influenza A virus (IAV) defective interfering particles (DIPs) are considered as new promising antiviral agents. Conventional DIPs (cDIPs) contain a deletion in the genome and can only replicate upon co-infection with infectious standard virus (STV), during which they suppress STV replication. We previously discovered a new type of IAV DIP “OP7” that entails genomic point mutations and displays higher antiviral efficacy than cDIPs. To avoid safety concerns for the medical use of OP7 preparations, we developed a production system that does not depend on infectious IAV. We reconstituted a mixture of DIPs consisting of cDIPs and OP7 chimera DIPs, in which both harbor a deletion in their genome. To complement the defect, the deleted viral protein is expressed by the suspension cell line used for production in shake flasks. Here, DIP preparations harvested are not contaminated with infectious virions, and the fraction of OP7 chimera DIPs depended on the multiplicity of infection. Intranasal administration of OP7 chimera DIP material was well tolerated in mice. A rescue from an otherwise lethal IAV infection and no signs of disease upon OP7 chimera DIP co-infection demonstrated the remarkable antiviral efficacy. The clinical development of this new class of broad-spectrum antiviral may contribute to pandemic preparedness. |
format | Online Article Text |
id | pubmed-10684881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106848812023-11-30 Generation of “OP7 chimera” defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice Dogra, Tanya Pelz, Lars Boehme, Julia D. Kuechler, Jan Kershaw, Olivia Marichal-Gallardo, Pavel Baelkner, Maike Hein, Marc D. Gruber, Achim D. Benndorf, Dirk Genzel, Yvonne Bruder, Dunja Kupke, Sascha Y. Reichl, Udo Sci Rep Article Influenza A virus (IAV) defective interfering particles (DIPs) are considered as new promising antiviral agents. Conventional DIPs (cDIPs) contain a deletion in the genome and can only replicate upon co-infection with infectious standard virus (STV), during which they suppress STV replication. We previously discovered a new type of IAV DIP “OP7” that entails genomic point mutations and displays higher antiviral efficacy than cDIPs. To avoid safety concerns for the medical use of OP7 preparations, we developed a production system that does not depend on infectious IAV. We reconstituted a mixture of DIPs consisting of cDIPs and OP7 chimera DIPs, in which both harbor a deletion in their genome. To complement the defect, the deleted viral protein is expressed by the suspension cell line used for production in shake flasks. Here, DIP preparations harvested are not contaminated with infectious virions, and the fraction of OP7 chimera DIPs depended on the multiplicity of infection. Intranasal administration of OP7 chimera DIP material was well tolerated in mice. A rescue from an otherwise lethal IAV infection and no signs of disease upon OP7 chimera DIP co-infection demonstrated the remarkable antiviral efficacy. The clinical development of this new class of broad-spectrum antiviral may contribute to pandemic preparedness. Nature Publishing Group UK 2023-11-28 /pmc/articles/PMC10684881/ /pubmed/38017026 http://dx.doi.org/10.1038/s41598-023-47547-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Dogra, Tanya Pelz, Lars Boehme, Julia D. Kuechler, Jan Kershaw, Olivia Marichal-Gallardo, Pavel Baelkner, Maike Hein, Marc D. Gruber, Achim D. Benndorf, Dirk Genzel, Yvonne Bruder, Dunja Kupke, Sascha Y. Reichl, Udo Generation of “OP7 chimera” defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice |
title | Generation of “OP7 chimera” defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice |
title_full | Generation of “OP7 chimera” defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice |
title_fullStr | Generation of “OP7 chimera” defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice |
title_full_unstemmed | Generation of “OP7 chimera” defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice |
title_short | Generation of “OP7 chimera” defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice |
title_sort | generation of “op7 chimera” defective interfering influenza a particle preparations free of infectious virus that show antiviral efficacy in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684881/ https://www.ncbi.nlm.nih.gov/pubmed/38017026 http://dx.doi.org/10.1038/s41598-023-47547-1 |
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