Evidence map›Paper›PMID 33216132›Full record

ArticleThe Journal of infectious diseases2021

Longitudinal Dynamics of Intact HIV Proviral DNA and Outgrowth Virus Frequencies in a Cohort of Individuals Receiving Antiretroviral Therapy.

Shane D Falcinelli, Kayla W Kilpatrick, Jenna Read, Ross Murtagh, Brigitte Allard, Simon Ghofrani, Jennifer Kirchherr, Katherine S James, Erin Stuelke, Caroline Baker and 6 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
6.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 79 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Shane D FalcinelliUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Kayla W KilpatrickBiostatistics Core, Center for AIDS Research, University of North Carolina, Chapel Hill, North Carolina, USA.
Jenna ReadUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Ross MurtaghUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Brigitte AllardUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Simon GhofraniUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Jennifer KirchherrUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Katherine S JamesUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Erin StuelkeUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Caroline BakerUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
JoAnn D KurucUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Joseph J EronDepartment of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
Michael G HudgensBiostatistics Core, Center for AIDS Research, University of North Carolina, Chapel Hill, North Carolina, USA.
Cynthia L GayUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
David M MargolisUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
Nancie M ArchinUniversity of North Carolina HIV Cure Center, University of North Carolina, Chapel Hill, North Carolina, USA.
University of North Carolina at Chapel Hill · USJohns Hopkins University Center for AIDS Research

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Collaboratory of AIDS Researchers for Eradication (CARE)UM1AI126619 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MARGOLIS, DAVID M. · 2016 to 2020
$23.2M
The HIV Reservoir in Women: Implications for HIV cure interventionsR01AI134363 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ARCHIN, NANCIE MARIE · 2017 to 2020
$2.2M
Reducing the HIV Reservoir: Next-Generation Latency Reversal Agents and T Cell Population TargetsF30AI145588 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FALCINELLI, SHANE DAVID · 2019 to 2023
$217k
NIAID NIH HHS F30 AI145588NIAID NIH HHS P30 AI050410NIAID NIH HHS R01 AI134363NIAID NIH HHS UM1 AI126619
6 · The paper itself

Abstract

backgroundThe replication-competent human immunodeficiency virus (HIV) reservoir is the major barrier to cure. The quantitative viral outgrowth assay (QVOA), the gold-standard method to quantify replication-competent HIV, is resource intensive, which limits its application in large clinical trials. The intact proviral DNA assay (IPDA) requires minimal cell input relative to QVOA and quantifies both defective and intact proviral HIV DNA, the latter potentially serving as a surrogate marker for replication-competent provirus. However, there are limited cross-sectional and longitudinal data on the relationship between IPDA and QVOA measurements.

methodsQVOA and IPDA measurements were performed on 156 resting CD4 T-cell (rCD4) samples from 83 antiretroviral therapy-suppressed HIV-positive participants. Longitudinal QVOA and IPDA measurements were performed on rCD4 from 29 of these participants.

resultsFrequencies of intact, defective, and total proviruses were positively associated with frequencies of replication-competent HIV. Longitudinally, decreases in intact proviral frequencies were strikingly similar to that of replication-competent virus in most participants. In contrast, defective proviral DNA frequencies appeared relatively stable over time in most individuals.

conclusionsChanges in frequencies of IPDA-derived intact proviral DNA and replication-competent HIV measured by QVOA are similar. IPDA is a promising high-throughput approach to estimate changes in the frequency of the replication-competent reservoir.

Indexed as

AdultAnti-Retroviral AgentsCross-Sectional StudiesDNA, ViralFemaleHIVHumansLongitudinal StudiesMaleMiddle AgedProvirusesRetrospective StudiesAnti-Retroviral AgentsDNA, ViralcuredecayHIVIPDAlongitudinalQVOAreservoir

Identifiers

PMID33216132
PMCPMC8253129
OpenAlexW3102823118

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.