Evidence map›Paper›PMID 25904747›Full record

Trial reportSexually transmitted infections2015

Decreased monocyte activation with daily acyclovir use in HIV-1/HSV-2 coinfected women.

Andrew D Redd, Kevin Newell, Eshan U Patel, Fred Nalugoda, Paschal Ssebbowa, Sarah Kalibbala, Melanie A Frank, Aaron A R Tobian, Ronald H Gray, Thomas C Quinn and 2 more

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Sexually transmitted infections, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00405821 (A Randomized, Double-Blind, Placebo-Controlled Trial of Acyclovir Prophylaxis Versus Placebo Among HIV-1/HSV-2 Co-Infected Individuals in Uganda), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 23% 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.

NCT00405821 phase2completednot on this map

A Randomized, Double-Blind, Placebo-Controlled Trial of Acyclovir Prophylaxis Versus Placebo Among HIV-1/HSV-2 Co-Infected Individuals in Uganda

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2006 to 2010Enrolled440ConditionsHIV Infections, Herpes GenitalisArmsAcyclovir, Placebo
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
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

12 authors at 7 institutions in 2 countries.

Andrew D ReddDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Kevin NewellFrederick National Laboratory for Cancer Research, Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Frederick, Maryland, USA.
Eshan U PatelDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Fred NalugodaRakai Health Sciences Program, Entebbe, Uganda.
Paschal SsebbowaRakai Health Sciences Program, Entebbe, Uganda.
Sarah KalibbalaRakai Health Sciences Program, Entebbe, Uganda.
Melanie A FrankDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Aaron A R TobianDepartment of Pathology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Ronald H GrayDepartment of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA.
Thomas C QuinnDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
David SerwaddaRakai Health Sciences Program, Entebbe, Uganda Institute of Public Health, Makerere University, Kampala, Uganda.
Steven J ReynoldsDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Rakai Health Sciences Program · UGJohns Hopkins University · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USFrederick National Laboratory for Cancer Research · USJohns Hopkins Medicine · USMakerere University · UG

Funding

International Center for Excellence in Research (ICER) in Uganda: Impact of ARVsZIAAI001040 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI REYNOLDS, STEVEN · 2009 to 2025
$23.5M
International Studies of the Acquired Immune Deficiency Syndrome (AIDS)ZIAAI000361 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI REDD, ANDREW · 2009 to 2025
$15.8M
International Center for Excellence in Research (ICER) in Uganda: Impact of ARVsZ01AI001040 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI QUINN, THOMAS · 2008 to 2008
$2.2M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z01 AI001040Intramural NIH HHS Z99 AI999999NCI NIH HHS HHSN261200800001ENIAID NIH HHS AI001040
6 · The paper itself

Abstract

objectivesSeveral clinical trials have demonstrated that daily treatment of HIV-infected individuals with the antiherpes drug acyclovir slightly decreases HIV-1 viral load and slows disease progression. This study examines if this slowing in clinical progression is a direct cause of the decrease in viral load or an indirect effect of lower immune activation due to lower levels of herpetic reactivation.

methodsWomen who participated in a randomised clinical trial of daily acyclovir use (n=301) were monitored every 6 months for changes in immune activation. Soluble CD14 (sCD14), a marker for monocyte activation, and C-reactive protein (CRP), a marker for general immune activation, were measured by ELISA.

resultsInitial levels of sCD14 and CRP were not predictive of HIV disease progression when controlling for initial CD4+ cell count and HIV viral load. sCD14 levels, but not CRP, decreased in the acyclovir treatment arm at a significantly faster rate than the placebo group, which was independent of changes in HIV viral load and CD4+ cell count in a multivariant mixed-effects model (p=0.039). However, the magnitude of this decrease was relatively small with a total estimated decrease of sCD14 of 15% of initial levels.

conclusionsThese data suggest that decreased monocyte activation may play a minor role in the ability of daily acyclovir use to slow HIV disease progression. CLINICAL TRIAL REGISTRATION NUMBER: NCT00405821.

Indexed as

AcyclovirAdultAntiviral AgentsC-Reactive ProteinDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleHerpes GenitalisHerpesvirus 2, HumanHIV-1HIV InfectionsHumansLipopolysaccharide ReceptorsMiddle AgedMonocytesYoung AdultAcyclovirAntiviral AgentsC-Reactive ProteinLipopolysaccharide ReceptorsHERPESHERPES SIMPLEX (CLINICAL)HIVHIV IMMUNOLOGYHSV THERAPEUTICS

Identifiers

PMID25904747
PMCPMC11044024
OpenAlexW2166062307

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.