Evidence map›Paper›PMID 23658114›Full record

Trial reportJournal of the Royal Society, Interface2013

Modelling HIV-1 2-LTR dynamics following raltegravir intensification.

Rutao Luo, E Fabian Cardozo, Michael J Piovoso, Hulin Wu, Maria J Buzon, Javier Martinez-Picado, Ryan Zurakowski

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the Royal Society, Interface, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Modeling HIV persistence and cure studies.Current opinion in HIV and AIDS · 2018
    Review
  11. Article
  12. Review
  13. Article
  14. Implications of Measurement Assay Type in Design of HIV Experiments.Proceedings of the ... IEEE Conference on Decision & Control. IEEE Conference on Decision & Control · 2017
    Article
  15. Experiment Design for Early Molecular Events in HIV Infection.Proceedings of the ... American Control Conference. American Control Conference · 2017
    Article
  16. Order preservation of expected information content using Unscented Transform approximation of multivariate prior distributions in HIV 2-LTR experiment design.Proceedings of the ... IEEE Conference on Decision & Control. IEEE Conference on Decision & Control · 2016
    Article
  17. Article
  18. Review
  19. Prospective HIV Clinical Trial Comparison by Expected Kullback-Leibler Divergence.Proceedings of the ... American Control Conference. American Control Conference · 2016
    Article
  20. Article
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

7 authors.

Rutao LuoDepartment of Electrical and Computer Engineering, University of Delaware, Newark, DE, USA.
E Fabian Cardozo
Michael J Piovoso
Hulin Wu
Maria J Buzon
Javier Martinez-Picado
Ryan Zurakowski

Funding

Virology/Immunology CoreP30AI078498 · NIAID · UNIVERSITY OF ROCHESTER · PI DEWHURST, STEPHEN · 2008 to 2018
$14.6M
Statistical Methods for ODE Models in AIDS ResearchR01AI087135 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, HULIN · 2010 to 2019
$3.2M
Analysis of Differential Resistance Emergence Risk for Differential Treatment AppR21AI078842 · NIAID · UNIVERSITY OF DELAWARE · PI ZURAKOWSKI, RYAN M · 2009 to 2010
$396k
NIAID NIH HHS P30 AI078498NIAID NIH HHS R01 AI087135NIAID NIH HHS R01AI087135NIAID NIH HHS R21 AI078842NIAID NIH HHS R21AI078842
6 · The paper itself

Abstract

A model of reservoir activation and viral replication is introduced accounting for the production of 2-LTR HIV-1 DNA circles following antiviral intensification with the HIV integrase inhibitor raltegravir, considering contributions of de novo infection events and exogenous sources of infected cells, including quiescent infected cell activation. The model shows that a monotonic increase in measured 2-LTR concentration post intensification is consistent with limited de novo infection primarily maintained by sources of infected cells unaffected by raltegravir, such as quiescent cell activation, while a transient increase in measured 2-LTR concentration is consistent with significant levels of efficient (R0 > 1) de novo infection. The model is validated against patient data from the INTEGRAL study and is shown to have a statistically significant fit relative to the null hypothesis of random measurement variation about a mean. We obtain estimates and confidence intervals for the model parameters, including 2-LTR half-life. Seven of the 13 patients with detectable 2-LTR concentrations from the INTEGRAL study have measured 2-LTR dynamics consistent with significant levels of efficient replication of the virus prior to treatment intensification.

Indexed as

Models, BiologicalAntiretroviral Therapy, Highly ActiveDisease ReservoirsDNA, CircularDNA, ViralHIV-1HIV InfectionsHumansPyrrolidinonesRaltegravir PotassiumTime FactorsVirus ReplicationDNA, CircularDNA, ViralPyrrolidinonesRaltegravir Potassiumcryptic viremiaHIVmathematical biology

Identifiers

PMID23658114
PMCPMC3673152

What OpenQuestion holds

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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.