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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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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. |
format | Online Article Text |
id | pubmed-10144178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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