APOBEC3G-depleted resting CD4+ T cells remain refractory to HIV1 infection.
<h4>Background</h4>CD4+ T lymphocytes are the primary targets of HIV1 but cannot be infected when fully quiescent, due to a post-entry block preventing the completion of reverse transcription. Chiu et al. recently proposed that this restriction reflects the action of APOBEC3G (A3G). They...
Guardado en:
Autores principales: | Francesca R Santoni de Sio, Didier Trono |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2009
|
Materias: | |
Acceso en línea: | https://doaj.org/article/1b1000cfba5c4167bed75b030dedd744 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Prestimulation of CD2 confers resistance to HIV-1 latent infection in blood resting CD4 T cells
por: Sijia He, et al.
Publicado: (2021) -
Directly infected resting CD4+T cells can produce HIV Gag without spreading infection in a model of HIV latency.
por: Matthew J Pace, et al.
Publicado: (2012) -
RNA-dependent oligomerization of APOBEC3G is required for restriction of HIV-1.
por: Hendrik Huthoff, et al.
Publicado: (2009) -
Apobec 3G efficiently reduces infectivity of the human exogenous gammaretrovirus XMRV.
por: Kristin Stieler, et al.
Publicado: (2010) -
The role of innate APOBEC3G and adaptive AID immune responses in HLA-HIV/SIV immunized SHIV infected macaques.
por: Yufei Wang, et al.
Publicado: (2012)