Evidence map›Paper›PMID 26425694›Full record

ArticleEBioMedicine2015

A Novel Assay to Measure the Magnitude of the Inducible Viral Reservoir in HIV-infected Individuals.

Francesco Andrea Procopio, Rémi Fromentin, Deanna A Kulpa, Jessica H Brehm, Anne-Gaelle Bebin, Matthew C Strain, Douglas D Richman, Una O'Doherty, Sarah Palmer, Frederick M Hecht and 7 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 194 papers.

0numbers the graph read from it
0cells of the map it votes in
194citing papers in PubMed
15.9field-weighted citation impact, top 1% 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

194 citing papers in PubMed, 263 citations in OpenAlex.

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  18. HIV-1 latency reversal agent boosting is not limited by opioid use.medRxiv : the preprint server for health sciences · 2024
    Article
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134 more citing papers are in PubMed but not listed here.

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

17 authors at 7 institutions in 2 countries.

Francesco Andrea ProcopioVaccine and Gene Therapy Institute Florida, Port St. Lucie, FL, USA.
Rémi FromentinVaccine and Gene Therapy Institute Florida, Port St. Lucie, FL, USA.
Deanna A KulpaVaccine and Gene Therapy Institute Florida, Port St. Lucie, FL, USA.
Jessica H BrehmVaccine and Gene Therapy Institute Florida, Port St. Lucie, FL, USA.
Anne-Gaelle BebinVaccine and Gene Therapy Institute Florida, Port St. Lucie, FL, USA.
Matthew C StrainUniversity of California San Diego, La Jolla, California and Veterans Affairs San Diego Healthcare System, San Diego, CA, USA.
Douglas D RichmanUniversity of California San Diego, La Jolla, California and Veterans Affairs San Diego Healthcare System, San Diego, CA, USA.
Una O'DohertyDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Sarah PalmerCentre for Virus Research, Westmead Millennium Institute, Westmead, Australia ; Sydney Medical School, University of Sydney, Sydney, Australia.
Frederick M HechtDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
Rebecca HohDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
Richard J O BarnardInfectious Disease, Merck Research Laboratories, West Point, PA, USA.
Michael D MillerInfectious Disease, Merck Research Laboratories, West Point, PA, USA.
Daria J HazudaInfectious Disease, Merck Research Laboratories, West Point, PA, USA.
Steven G DeeksDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
Rafick-Pierre SékalyVaccine and Gene Therapy Institute Florida, Port St. Lucie, FL, USA.
Nicolas ChomontVaccine and Gene Therapy Institute Florida, Port St. Lucie, FL, USA.
Vaccine & Gene Therapy Institute of Florida · USUnited States Military Academy · USUniversity of California, San Francisco · USUniversity of California, San Diego · USUniversity of Pennsylvania · USUniversity of Sydney · AUVA San Diego Healthcare System · US

Funding

Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVEN Grant DEEKS · 1988 to 2026
$93.6M
Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROBERT GROSS · 1999 to 2026
$78.6M
Viral reservoirs and sanctuaries in HAART - treated patients: role and mechanismsU19AI096109 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DEEKS, STEVEN GRANT · 2011 to 2015
$29.5M
TILDA: A new sensitive and precise assay to measure the size of the latent HIV reservoirR21AI113096 · NIAID · VGTI FLORIDA · PI CHOMONT, NICOLAS · 2014 to 2015
$334k
NIAID NIH HHS P30 AI027763NIAID NIH HHS P30 AI045008NIAID NIH HHS R21 AI113096NIAID NIH HHS U19 AI096109
6 · The paper itself

Abstract

backgroundQuantifying latently infected cells is critical to evaluate the efficacy of therapeutic strategies aimed at reducing the size of the long-lived viral reservoir, but the low frequency of these cells makes this very challenging.

methodsWe developed TILDA (Tat/rev Induced Limiting Dilution Assay) to measure the frequency of cells with inducible multiply-spliced HIV RNA, as these transcripts are usually absent in latently infected cells but induced upon viral reactivation. TILDA requires less than a million cells, does not require RNA extraction and can be completed in two days.

findingsIn suppressed individuals on ART, we found the median frequency of latently infected CD4 + T cells as estimated by TILDA to be 24 cells/million, which was 48 times more than the frequency measured by the quantitative viral outgrowth assay, and 6-27 times less than the frequencies of cells harbouring viral DNA measured by PCR-based assays. TILDA measurements strongly correlated with most HIV DNA assays. The size of the latent reservoir measured by TILDA was lower in subjects who initiated ART during the early compared to late stage of infection (p = 0.011). In untreated HIV disease, the frequency of CD4 + cells carrying latent but inducible HIV largely exceeded the frequency of actively producing cells, demonstrating that the majority of infected cells are transcriptionally silent even in the absence of ART. INTERPRETATIONS: Our results suggest that TILDA is a reproducible and sensitive approach to measure the frequency of productively and latently infected cells in clinical settings. We demonstrate that the latent reservoir represents a substantial fraction of all infected cells prior to ART initiation. RESEARCH IN CONTEXT: In this manuscript, we describe the development of a novel assay that measures the magnitude of the latent HIV reservoir, the main barrier to HIV eradication. This novel assay, termed TILDA for Tat/rev Induced Limiting Dilution Assay, requires only 10 ml of blood, does not necessitate extraction of viral nucleic acids, is highly reproducible, covers a wide dynamic range of reservoir sizes and can be completed in two days. As such, TILDA may represent an alternative to existing assays used to evaluate the efficacy of therapeutic strategies aimed at reducing the size of the latent HIV reservoir.

Indexed as

Virus LatencyAdultAnti-Retroviral AgentsCD4-Positive T-LymphocytesDNA, ViralFemaleHIV-1HIV InfectionsHumansMaleMiddle AgedRNA, ViralAnti-Retroviral AgentsDNA, ViralRNA, ViralEradicationHIVInducible virusLatencyMultiply spliced RNAReservoirTILDA

Identifiers

PMID26425694
PMCPMC4563128
OpenAlexW2117633297

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.