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dc.creatorDe Oliveira, MF
dc.creatorGianella, S
dc.creatorLetendre, S
dc.creatorScheffler, K
dc.creatorPond, SLK
dc.creatorSmith, DM
dc.creatorStrain, M
dc.creatorEllis, RJ
dc.date.accessioned2021-01-29T17:53:34Z
dc.date.available2021-01-29T17:53:34Z
dc.date.issued2015-10-02
dc.identifier.issn1932-6203
dc.identifier.issn1932-6203
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/5172
dc.identifier.other26431315 (pubmed)
dc.identifier.urihttp://hdl.handle.net/20.500.12613/5190
dc.description.abstractBackground Measurement of HIV DNA-bearing cells in cerebrospinal fluid (CSF) is challenging because few cells are present. We present a novel application of the sensitive droplet digital (dd) PCR in this context. Methods We analyzed CSF cell pellets and paired peripheral blood mononuclear cells (PBMC) from 28 subjects, 19 of whom had undetectable HIV RNA (<48 copies/mL) in both compartments. We extracted DNA from PBMC using silica-based columns and used direct lysis on CSF cells. HIV DNA and the host housekeeping gene (RPP30) were measured in CSF and PBMC by (dd)PCR. We compared HIV DNA levels in virally-suppressed and-unsuppressed subgroups and calculated correlations between HIV DNA and RNA levels in both compartments using non-parametric tests. Results HIV DNA was detected in 18/28 (64%) CSF cell pellets, including 10/19 (53%) samples with undetectable HIV RNA. HIV DNA levels in CSF cell pellets were not correlated with RPP30 (p = 0.3), but correlated positively with HIV RNA in CSF (p = 0.04) and HIV DNA in PBMC (p = 0.03). Cellular HIV DNA in CSF was detected in comparable levels in HIV RNA-suppressed and unsuppressed subjects (p = 0.14). In contrast, HIV DNA levels in PBMC were significantly lower in HIV RNA-suppressed than in unsuppressed subjects (p = 0.014). Among subjects with detectable HIV DNA in both compartments, HIV DNA levels in CSF were significantly higher than in PBMC (p<0.001). Conclusions Despite low mononuclear cell numbers in CSF, HIV DNA was detected in most virally suppressed individuals. In contrast to PBMC, suppressive ART was not associated with lower HIV DNA levels in CSF cells, compared to no ART, perhaps due to poorer ART penetration, slower decay of HIV DNA, or enrichment of HIV DNA-bearing mononuclear cells into the CSF, compared to blood. Future studies should determine what fraction of HIV DNA is replication- competent in CSF leukocytes, compared to PBMC.
dc.format.extente0139510-e0139510
dc.language.isoen
dc.relation.haspartPLoS ONE
dc.relation.isreferencedbyPublic Library of Science (PLoS)
dc.rights.urihttps://creativecommons.org/publicdomain/zero/1.0/
dc.subjectAnti-HIV Agents
dc.subjectAntiretroviral Therapy, Highly Active
dc.subjectCD4-Positive T-Lymphocytes
dc.subjectCerebrospinal Fluid
dc.subjectDNA, Viral
dc.subjectHIV Infections
dc.subjectHIV-1
dc.subjectHumans
dc.subjectLeukocytes, Mononuclear
dc.subjectOrgan Specificity
dc.subjectPolymerase Chain Reaction
dc.subjectRNA, Viral
dc.subjectRetrospective Studies
dc.subjectViral Load
dc.subjectViremia
dc.subjectVirus Replication
dc.titleComparative analysis of cell-associated HIV DNA levels in cerebrospinal fluid and peripheral blood by droplet digital PCR
dc.typeArticle
dc.type.genreJournal Article
dc.relation.doi10.1371/journal.pone.0139510
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.creator.orcidPond, Sergei L. Kosakovsky|0000-0003-4817-4029
dc.date.updated2021-01-29T17:53:31Z
refterms.dateFOA2021-01-29T17:53:35Z


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