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CD34T+ Humanized Mouse Model to Study Mucosal HIV-1 Transmission and Prevention
- 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.
- Subjects :
- 0301 basic medicine
T cell
Immunology
lcsh:Medicine
Article
03 medical and health sciences
0302 clinical medicine
In vivo
Drug Discovery
medicine
Pharmacology (medical)
Pharmacology
biology
business.industry
mucosal HIV-1 prevention
broadly neutralizing antibodies
lcsh:R
3. Good health
Mucosal Infection
030104 developmental biology
Infectious Diseases
medicine.anatomical_structure
Lymphatic system
humanized mice
Viral replication
030220 oncology & carcinogenesis
Cord blood
Humanized mouse
biology.protein
Antibody
business
Subjects
Details
- Language :
- English
- ISSN :
- 2076393X
- Database :
- OpenAIRE
- Journal :
- Vaccines
- Accession number :
- edsair.doi.dedup.....99324ff134a2f69a718611cacb047f4f
- Full Text :
- https://doi.org/10.3390/vaccines9030198