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SAMHD1: a new contributor to HIV-1 restriction in resting CD4(+) T-cells
Resting CD4(+) T-cells are critical for establishing HIV-1 reservoirs. It has been known for over two decades that resting CD4(+) T-cells are refractory to HIV-1 infection, but the underlying mechanisms are not fully understood. Compared with activated CD4(+) T-cells that support HIV-1 infection, re...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492151/ https://www.ncbi.nlm.nih.gov/pubmed/23092163 http://dx.doi.org/10.1186/1742-4690-9-88 |
Sumario: | Resting CD4(+) T-cells are critical for establishing HIV-1 reservoirs. It has been known for over two decades that resting CD4(+) T-cells are refractory to HIV-1 infection, but the underlying mechanisms are not fully understood. Compared with activated CD4(+) T-cells that support HIV-1 infection, resting CD4(+) T-cells have lower levels of dNTPs, which limit HIV-1 reverse transcription. The dNTPase SAMHD1 has been identified as an HIV-1 restriction factor in non-cycling myeloid cells. Two recent studies revealed that SAMHD1 restricts HIV-1 infection in resting CD4(+) T-cells, suggesting a common mechanism of HIV-1 restriction in non-cycling cells that may contribute to viral immunopathogenesis. |
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