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Limited HIV-2 reservoirs in central-memory CD4 T-cells associated to CXCR6 co-receptor expression in attenuated HIV-2 infection
dc.rights.license | open | en_US |
dc.contributor.author | SAMRI, A. | |
dc.contributor.author | CHARPENTIER, C. | |
dc.contributor.author | DIALLO, M. | |
dc.contributor.author | BERTINE, M. | |
dc.contributor.author | EVEN, S. | |
dc.contributor.author | MORIN, V. | |
dc.contributor.author | OUDIN, A. | |
dc.contributor.author | PARIZOT, C. | |
dc.contributor.author | COLLIN, G. | |
dc.contributor.author | HOSMALIN, A. | |
dc.contributor.author | CHEYNIER, R. | |
hal.structure.identifier | Statistics In System biology and Translational Medicine [SISTM] | |
hal.structure.identifier | Bordeaux population health [BPH] | |
dc.contributor.author | THIEBAUT, Rodolphe | |
dc.contributor.author | MATHERON, S. | |
hal.structure.identifier | Statistics In System biology and Translational Medicine [SISTM] | |
hal.structure.identifier | Bordeaux population health [BPH] | |
dc.contributor.author | COLLIN, Fideline | |
dc.contributor.author | ZOOROB, R. | |
dc.contributor.author | BRUN-VEZINET, F. | |
dc.contributor.author | AUTRAN, B. | |
dc.date.accessioned | 2020-07-13T11:55:17Z | |
dc.date.available | 2020-07-13T11:55:17Z | |
dc.date.issued | 2019-05-16 | |
dc.identifier.issn | 1553-7366 | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/10432 | |
dc.description.abstractEn | The low pathogenicity and replicative potential of HIV-2 are still poorly understood. We investigated whether HIV-2 reservoirs might follow the peculiar distribution reported in models of attenuated HIV-1/SIV infections, i.e. limited infection of central-memory CD4 T lymphocytes (TCM). Antiretroviral-naive HIV-2 infected individuals from the ANRS-CO5 (12 non-progressors, 2 progressors) were prospectively included. Peripheral blood mononuclear cells (PBMCs) were sorted into monocytes and resting CD4 T-cell subsets (naive [TN], central- [TCM], transitional- [TTM] and effector-memory [TEM]). Reactivation of HIV-2 was tested in 30-day cultures of CD8-depleted PBMCs. HIV-2 DNA was quantified by real-time PCR. Cell surface markers, co-receptors and restriction factors were analyzed by flow-cytometry and multiplex transcriptomic study. HIV-2 DNA was undetectable in monocytes from all individuals and was quantifiable in TTM from 4 individuals (median: 2.25 log10 copies/106 cells [IQR: 1.99-2.94]) but in TCM from only 1 individual (1.75 log10 copies/106 cells). HIV-2 DNA levels in PBMCs (median: 1.94 log10 copies/106 PBMC [IQR = 1.53-2.13]) positively correlated with those in TTM (r = 0.66, p = 0.01) but not TCM. HIV-2 reactivation was observed in the cells from only 3 individuals. The CCR5 co-receptor was distributed similarly in cell populations from individuals and donors. TCM had a lower expression of CXCR6 transcripts (p = 0.002) than TTM confirmed by FACS analysis, and a higher expression of TRIM5 transcripts (p = 0.004). Thus the low HIV-2 reservoirs differ from HIV-1 reservoirs by the lack of monocytic infection and a limited infection of TCM associated to a lower expression of a potential alternative HIV-2 co-receptor, CXCR6 and a higher expression of a restriction factor, TRIM5. These findings shed new light on the low pathogenicity of HIV-2 infection suggesting mechanisms close to those reported in other models of attenuated HIV/SIV infection models. | |
dc.language.iso | EN | en_US |
dc.rights | Attribution 3.0 United States | |
dc.rights.uri | https://creativecommons.org/licenses/by/3.0/us/ | |
dc.subject.en | SISTM | |
dc.title.en | Limited HIV-2 reservoirs in central-memory CD4 T-cells associated to CXCR6 co-receptor expression in attenuated HIV-2 infection | |
dc.title.alternative | PLoS Pathog | en_US |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.1371/journal.ppat.1007758 | |
dc.subject.hal | Sciences du Vivant [q-bio]/Santé publique et épidémiologie | en_US |
dc.identifier.pubmed | 31095640 | en_US |
bordeaux.journal | Plos Pathogens | en_US |
bordeaux.page | e1007758 | en_US |
bordeaux.volume | 15 | en_US |
bordeaux.hal.laboratories | Bordeaux Population Health Research Center (BPH) - UMR 1219 | en_US |
bordeaux.issue | 5 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.team | SISTM_BPH | |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
hal.identifier | hal-03160709 | |
hal.version | 1 | |
hal.date.transferred | 2021-03-15T09:17:19Z | |
hal.export | true | |
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