Evidence map›Paper›PMID 27045377›Full record

ArticleAIDS (London, England)2016

The plasma levels of soluble ST2 as a marker of gut mucosal damage in early HIV infection.

Vikram Mehraj, Mohammad-Ali Jenabian, Rosalie Ponte, Bertrand Lebouché, Cecilia Costiniuk, Réjean Thomas, Jean-Guy Baril, Roger LeBlanc, Joseph Cox, Cécile Tremblay and 2 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in AIDS (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04058392 (FULL TITLE), which is not on this map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.6field-weighted citation impact, top 7% 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.

NCT04058392 phase1completednot on this mapstarted 2020, after this paper: background citation

FULL TITLE: Camu Camu Effects on Circulating LPS and Systemic Immune Activation in ART-treated Participants: the Camu Camu Pilot Study

TypeinterventionalSponsorMcGill University Health Centre/Research Institute of the McGill University Health CentreRan2020 to 2022Enrolled22ConditionsHIV InfectionsArmsCamu Camu Capsules
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 37 citations in OpenAlex.

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  7. Circulating (1→3)-β-D-glucan Is Associated With Immune Activation During Human Immunodeficiency Virus Infection.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  8. Fungal Translocation: A Driving Force Behind the Occurrence of Non-AIDS Events?Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
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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

12 authors at 7 institutions in 3 countries.

Vikram MehrajaResearch Institute of the McGill University Health CentrebChronic Viral Illness Service, McGill University Health CentrecDepartment of Biological Sciences and BioMed Research Centre, Université du Québec à Montréal (UQAM)dDepartment of Family Medicine, McGill UniversityeClinique Médicale l'ActuelfClinique Médicale Quartier LatingClinique Médicale OPUShCentre de recherche du Centre Hospitalier de l'Université de MontréaliDépartement de Microbiologie, Infectiologie et Immunologie, Université de MontréaljDivision of Hematology, McGill University Health Centre, Montréal, Québec, Canada.
Mohammad-Ali Jenabian
Rosalie Ponte
Bertrand Lebouché
Cecilia Costiniuk
Réjean Thomas
Jean-Guy Baril
Roger LeBlanc
Joseph Cox
Cécile Tremblay
Jean-Pierre Routy
Montreal Primary HIV Infection, the Canadian Long-Term Non-Progressors Study Groups
McGill University Health Centre · CACentre Hospitalier de l’Université de Montréal · CACHI Health Immanuel · USClinique Claude-Bernard · FRGTx (United States) · USMcGill University · CAUniversité du Québec à Montréal · CA

Funding

CIHR HIG-133050
6 · The paper itself

Abstract

objectiveFollowing tissue barrier breaches, interleukin-33 (IL-33) is released as an 'alarmin' to induce inflammation. Soluble suppression of tumorigenicity 2 (sST2), as an IL-33 decoy receptor, contributes to limit inflammation. We assessed the relationship between the IL-33/ST2 axis and markers of gut mucosal damage in patients with early (EHI) and chronic HIV infection (CHI) and elite controllers.

designAnalyses on patients with EHI and CHI were conducted to determine IL-33/sST2 changes over time.

methodsIL-33 and sST2 levels were measured in plasma. Correlations between sST2 levels and plasma viral load, CD4 and CD8 T-cell counts, expression of T-cell activation/exhaustion markers, gut mucosal damage, microbial translocation and inflammation markers, as well as kynurenine/tryptophan ratio were assessed.

resultsPlasma sST2 levels were elevated in EHI compared with untreated CHI and uninfected controls, whereas IL-33 levels were comparable in all groups. In EHI, sST2 levels were positively correlated with the CD8 T-cell count and the percentage of T cells expressing activation and exhaustion markers, but not with viral load or CD4 T-cell count. Plasma sST2 levels also correlated with plasma levels of gut mucosal damage, microbial translocation and kynurenine/tryptophan ratio and for some markers of inflammation. Prospective analyses showed that early antiretroviral therapy had no impact on sST2 levels, whereas longer treatment duration initiated during CHI normalized sST2.

conclusionAs sST2 levels were elevated in EHI and were correlated with CD8 T-cell count, immune activation, and microbial translocation, sST2 may serve as a marker of disease progression, gut damage and may directly contribute to HIV pathogenesis.

Indexed as

AdultBacterial TranslocationCross-Sectional StudiesFemaleHIV InfectionsHumansInterleukin-1 Receptor-Like 1 ProteinInterleukin-33Intestinal MucosaLymphocyte ActivationLymphocyte CountMaleMiddle AgedPlasmaT-LymphocytesViral LoadIL1RL1 protein, humanIL33 protein, humanInterleukin-1 Receptor-Like 1 ProteinInterleukin-33

Identifiers

PMID27045377
PMCPMC4900419
OpenAlexW2337166321

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.