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CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention

Authors :
Florian Klein
Daniela Weiland
Kathrin Held
Kanika Vanshylla
Christof Geldmacher
Kanika Jain
Ricarda Stumpf
Franziska Kleipass
Jan Münch
Berthold Grüttner
Henning Gruell
Tabea M. Eser
Source :
Vaccines, Volume 9, Issue 3, Vaccines, Vol 9, Iss 198, p 198 (2021)
Publication Year :
2021
Publisher :
Multidisciplinary Digital Publishing Institute, 2021.

Abstract

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.

Details

Language :
English
ISSN :
2076393X
Database :
OpenAIRE
Journal :
Vaccines
Accession number :
edsair.doi.dedup.....99324ff134a2f69a718611cacb047f4f
Full Text :
https://doi.org/10.3390/vaccines9030198