| Literature DB >> 33644255 |
Emilie Battivelli1,2,3, Eric Verdin1,2,3.
Abstract
While able to suppress HIV replication in HIV infected individuals, combination antiretroviral therapy (ART) fails to eliminate viral latent reservoir, which consists in integrated transcriptional silenced HIV provirus. So far, identification of latently-infected cells has relied on activating cells to induce expression of HIV proteins which can then be detected. Unfortunately, this activation significantly changed the cell phenotype. We developed a novel HIV reporter, named HIVGKO, that allows the purification of latently-infected cells in absence of reactivation. Indeed, latent cells can be identified by expression of the EF1a-driven mKO2 and lack of expression of the LTR-driven csGFP. This protocol can be used to study the effectiveness of LRAs (Latency Reversal Agents) in reactivating latent HIV in primary cells.Entities:
Keywords: Dual-fluorescence reporter; Flow cytometry; HIV-1 latency; HIVGKO; Human cells; Latency reversal; Latency reversal agents; Reservoirs
Year: 2018 PMID: 33644255 PMCID: PMC7909466 DOI: 10.21769/bioprotoc.3050
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325