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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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