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A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection

Individuals with Down syndrome (DS) are more prone to develop severe respiratory tract infections. Although a RSV infection has a high clinical impact and severe outcome in individuals with DS, no vaccine nor effective therapeutics are available. Any research into infection pathophysiology or prophy...

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Autores principales: Tielemans, Birger, De Herdt, Lander, Pollenus, Emilie, Vanhulle, Emiel, Seldeslachts, Laura, Marain, Fopke, Belmans, Flore, Ahookhosh, Kaveh, Vanoirbeek, Jeroen, Vermeire, Kurt, Van den Steen, Philippe E., Vande Velde, Greetje
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10144178/
https://www.ncbi.nlm.nih.gov/pubmed/37112973
http://dx.doi.org/10.3390/v15040993
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author Tielemans, Birger
De Herdt, Lander
Pollenus, Emilie
Vanhulle, Emiel
Seldeslachts, Laura
Marain, Fopke
Belmans, Flore
Ahookhosh, Kaveh
Vanoirbeek, Jeroen
Vermeire, Kurt
Van den Steen, Philippe E.
Vande Velde, Greetje
author_facet Tielemans, Birger
De Herdt, Lander
Pollenus, Emilie
Vanhulle, Emiel
Seldeslachts, Laura
Marain, Fopke
Belmans, Flore
Ahookhosh, Kaveh
Vanoirbeek, Jeroen
Vermeire, Kurt
Van den Steen, Philippe E.
Vande Velde, Greetje
author_sort Tielemans, Birger
collection PubMed
description Individuals with Down syndrome (DS) are more prone to develop severe respiratory tract infections. Although a RSV infection has a high clinical impact and severe outcome in individuals with DS, no vaccine nor effective therapeutics are available. Any research into infection pathophysiology or prophylactic and therapeutic antiviral strategies in the specific context of DS would greatly benefit this patient population, but currently such relevant animal models are lacking. This study aimed to develop and characterize the first mouse model of RSV infection in a DS-specific context. Ts65Dn mice and wild type littermates were inoculated with a bioluminescence imaging-enabled recombinant human RSV to longitudinally track viral replication in host cells throughout infection progression. This resulted in an active infection in the upper airways and lungs with similar viral load in Ts65Dn mice and euploid mice. Flow cytometric analysis of leukocytes in lungs and spleen demonstrated immune alterations with lower CD8+ T cells and B-cells in Ts65Dn mice. Overall, our study presents a novel DS-specific mouse model of hRSV infection and shows that potential in using the Ts65Dn preclinical model to study immune-specific responses of RSV in the context of DS and supports the need for models representing the pathological development.
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spelling pubmed-101441782023-04-29 A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection Tielemans, Birger De Herdt, Lander Pollenus, Emilie Vanhulle, Emiel Seldeslachts, Laura Marain, Fopke Belmans, Flore Ahookhosh, Kaveh Vanoirbeek, Jeroen Vermeire, Kurt Van den Steen, Philippe E. Vande Velde, Greetje Viruses Article Individuals with Down syndrome (DS) are more prone to develop severe respiratory tract infections. Although a RSV infection has a high clinical impact and severe outcome in individuals with DS, no vaccine nor effective therapeutics are available. Any research into infection pathophysiology or prophylactic and therapeutic antiviral strategies in the specific context of DS would greatly benefit this patient population, but currently such relevant animal models are lacking. This study aimed to develop and characterize the first mouse model of RSV infection in a DS-specific context. Ts65Dn mice and wild type littermates were inoculated with a bioluminescence imaging-enabled recombinant human RSV to longitudinally track viral replication in host cells throughout infection progression. This resulted in an active infection in the upper airways and lungs with similar viral load in Ts65Dn mice and euploid mice. Flow cytometric analysis of leukocytes in lungs and spleen demonstrated immune alterations with lower CD8+ T cells and B-cells in Ts65Dn mice. Overall, our study presents a novel DS-specific mouse model of hRSV infection and shows that potential in using the Ts65Dn preclinical model to study immune-specific responses of RSV in the context of DS and supports the need for models representing the pathological development. MDPI 2023-04-18 /pmc/articles/PMC10144178/ /pubmed/37112973 http://dx.doi.org/10.3390/v15040993 Text en © 2023 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
Tielemans, Birger
De Herdt, Lander
Pollenus, Emilie
Vanhulle, Emiel
Seldeslachts, Laura
Marain, Fopke
Belmans, Flore
Ahookhosh, Kaveh
Vanoirbeek, Jeroen
Vermeire, Kurt
Van den Steen, Philippe E.
Vande Velde, Greetje
A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection
title A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection
title_full A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection
title_fullStr A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection
title_full_unstemmed A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection
title_short A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection
title_sort multimodal imaging-supported down syndrome mouse model of rsv infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10144178/
https://www.ncbi.nlm.nih.gov/pubmed/37112973
http://dx.doi.org/10.3390/v15040993
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