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CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention
Humanized mice are critical for HIV-1 research, but humanized mice generated from cord blood are inefficient at mucosal HIV-1 transmission. Most mucosal HIV-1 transmission studies in mice require fetal tissue-engraftment, the use of which is highly restricted or prohibited. We present a fetal tissue...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997265/ https://www.ncbi.nlm.nih.gov/pubmed/33673566 http://dx.doi.org/10.3390/vaccines9030198 |
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author | Vanshylla, Kanika Held, Kathrin Eser, Tabea M. Gruell, Henning Kleipass, Franziska Stumpf, Ricarda Jain, Kanika Weiland, Daniela Münch, Jan Grüttner, Berthold Geldmacher, Christof Klein, Florian |
author_facet | Vanshylla, Kanika Held, Kathrin Eser, Tabea M. Gruell, Henning Kleipass, Franziska Stumpf, Ricarda Jain, Kanika Weiland, Daniela Münch, Jan Grüttner, Berthold Geldmacher, Christof Klein, Florian |
author_sort | Vanshylla, Kanika |
collection | PubMed |
description | Humanized mice are critical for HIV-1 research, but humanized mice generated from cord blood are inefficient at mucosal HIV-1 transmission. Most mucosal HIV-1 transmission studies in mice require fetal tissue-engraftment, the use of which is highly restricted or prohibited. We present a fetal tissue-independent model called CD34T+ with enhanced human leukocyte levels in the blood and improved T cell homing to the gut-associated lymphoid tissue. CD34T+ mice are highly permissive to intra-rectal HIV-1 infection and also show normal env diversification in vivo despite high viral replication. Moreover, mucosal infection in CD34T+ mice can be prevented by infusion of broadly neutralizing antibodies. CD34T+ mice can be rapidly and easily generated using only cord blood cells and do not require any complicated surgical procedures for the humanization process. Therefore, CD34T+ mice provide a novel platform for mucosal HIV-1 transmission studies as well as rapid in vivo testing of novel prevention molecules against HIV-1. |
format | Online Article Text |
id | pubmed-7997265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79972652021-03-27 CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention Vanshylla, Kanika Held, Kathrin Eser, Tabea M. Gruell, Henning Kleipass, Franziska Stumpf, Ricarda Jain, Kanika Weiland, Daniela Münch, Jan Grüttner, Berthold Geldmacher, Christof Klein, Florian Vaccines (Basel) Article Humanized mice are critical for HIV-1 research, but humanized mice generated from cord blood are inefficient at mucosal HIV-1 transmission. Most mucosal HIV-1 transmission studies in mice require fetal tissue-engraftment, the use of which is highly restricted or prohibited. We present a fetal tissue-independent model called CD34T+ with enhanced human leukocyte levels in the blood and improved T cell homing to the gut-associated lymphoid tissue. CD34T+ mice are highly permissive to intra-rectal HIV-1 infection and also show normal env diversification in vivo despite high viral replication. Moreover, mucosal infection in CD34T+ mice can be prevented by infusion of broadly neutralizing antibodies. CD34T+ mice can be rapidly and easily generated using only cord blood cells and do not require any complicated surgical procedures for the humanization process. Therefore, CD34T+ mice provide a novel platform for mucosal HIV-1 transmission studies as well as rapid in vivo testing of novel prevention molecules against HIV-1. MDPI 2021-02-27 /pmc/articles/PMC7997265/ /pubmed/33673566 http://dx.doi.org/10.3390/vaccines9030198 Text en © 2021 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 (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Vanshylla, Kanika Held, Kathrin Eser, Tabea M. Gruell, Henning Kleipass, Franziska Stumpf, Ricarda Jain, Kanika Weiland, Daniela Münch, Jan Grüttner, Berthold Geldmacher, Christof Klein, Florian CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention |
title | CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention |
title_full | CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention |
title_fullStr | CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention |
title_full_unstemmed | CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention |
title_short | CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention |
title_sort | cd34t+ humanized mouse model to study mucosal hiv-1 transmission and prevention |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997265/ https://www.ncbi.nlm.nih.gov/pubmed/33673566 http://dx.doi.org/10.3390/vaccines9030198 |
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