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Humanized Rag2(-/-)gammac(-/-) (RAG-hu) mice can sustain long-term chronic HIV-1 infection lasting more than a year.
- Source :
-
Virology [Virology] 2010 Feb 05; Vol. 397 (1), pp. 100-3. Date of Electronic Publication: 2009 Nov 18. - Publication Year :
- 2010
-
Abstract
- HIV-1 infection is characterized by life-long viral persistence and continued decline of helper CD4 T cells. The new generation of humanized mouse models that encompass RAG-hu, hNOG and BLT mice have been shown to be susceptible to HIV-1 infection and display CD4 T cell loss. Productive infection has been demonstrated with both R5 and X4 tropic strains of HIV-1 via direct injection as well as mucosal exposure. However the duration of infection in these mice was evaluated for a limited time lasting only weeks post infection, and it is not established how long the viremia can be sustained, and if the CD4 T cell loss persists throughout the life of the infected humanized mice. In the present study we followed the HIV-1 infected RAG-hu mice to determine the long-term viral persistence and CD4 T cell levels. Our results showed that viremia persists life-long lasting for more than a year, and that CD4 T cell levels display a continuous declining trend as seen in the human. These studies provide a chronic HIV-1 infection humanized mouse model that can be used to dissect viral latency, long-term drug evaluation and immune-based therapies.<br /> (Copyright 2009 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
CD4 Lymphocyte Count
HIV-1 growth & development
HIV-1 immunology
Humans
Mice
Mice, Inbred BALB C
Mice, Knockout
Mice, SCID
Time Factors
Viral Load
DNA-Binding Proteins deficiency
Disease Models, Animal
HIV Infections immunology
HIV Infections virology
HIV-1 pathogenicity
Immunoglobulin gamma-Chains genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0341
- Volume :
- 397
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Virology
- Publication Type :
- Academic Journal
- Accession number :
- 19922970
- Full Text :
- https://doi.org/10.1016/j.virol.2009.10.034