Evidence map›Paper›PMID 31504638›Full record

ArticleThe Journal of infectious diseases2020

Plasma Levels of C-Type Lectin REG3α and Gut Damage in People With Human Immunodeficiency Virus.

Stéphane Isnard, Rayoun Ramendra, Franck P Dupuy, John Lin, Brandon Fombuena, Nikola Kokinov, Ido Kema, Mohammad-Ali Jenabian, Bertrand Lebouché, Cecilia T Costiniuk and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

38 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

18 authors at 6 institutions in 3 countries.

Stéphane IsnardInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Rayoun RamendraInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Franck P DupuyInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
John LinInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Brandon FombuenaInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Nikola KokinovInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Ido KemaDepartment of Laboratory Medicine, University Medical Center, University of Groningen, The Netherlands.
Mohammad-Ali JenabianDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
Bertrand LebouchéInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Cecilia T CostiniukInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Petronela AncutaCentre de recherche du Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada.
Nicole F BernardInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Michael S SilvermanDepartment of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western University, London, Ontario.
Peter L LakatosDivision of Gastroenterology and Hepatology, McGill University Health Centre, McGill University Health Centre, Montreal, Quebec, Canada.
Madeleine DurandCentre de recherche du Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada.
Cécile TremblayCentre de recherche du Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada.
Jean-Pierre RoutyInfectious Diseases and Immunity in Global Health Program, Research Institute, McGill University, Montreal, Quebec, Canada.
Montreal Primary HIV Infection Study, the Canadian Cohort of HIV+ Slow Progressors, and the Canadian HIV and Aging Cohort Groups
McGill University Health Centre · CACHI Health Immanuel · USCentre Hospitalier de l’Université de Montréal · CAWestern University · CAUniversité du Québec à Montréal · CAUniversity Medical Center Groningen · NL

Funding

CIHR 154051CIHR HAL-157985CIHR HB2-164064CIHR HIG133050CIHR MOP 103230CIHR MOP93770CIHR PJT 166049CIHR TCO-125276
6 · The paper itself

Abstract

backgroundRegenerating islet-derived protein 3α (REG3α) is an antimicrobial peptide secreted by intestinal Paneth cells. Circulating REG3α has been identified as a gut damage marker in inflammatory bowel diseases. People living with human immunodeficiency virus (PWH) on antiretroviral therapy (ART) present with an abnormal intestinal landscape leading to microbial translocation, persistent inflammation, and development of non-AIDS comorbidities. Herein, we assessed REG3α as a marker of gut damage in PWH.

methodsPlasma from 169 adult PWH, including 30 elite controllers (ECs), and 30 human immunodeficiency virus (HIV)-uninfected controls were assessed. REG3α plasma levels were compared with HIV disease progression, epithelial gut damage, microbial translocation, and immune activation markers.

resultsCross-sectionally, REG3α levels were elevated in untreated and ART-treated PWH compared with controls. ECs also had elevated REG3α levels compared to controls. Longitudinally, REG3α levels increased in PWH without ART and decreased in those who initiated ART. REG3α levels were inversely associated with CD4 T-cell count and CD4:CD8 ratio, while positively correlated with HIV viral load in untreated participants, and with fungal product translocation and inflammatory markers in all PWH.

conclusionsPlasma REG3α levels were elevated in PWH, including ECs. The gut inflammatory marker REG3α may be used to evaluate therapeutic interventions and predict non-AIDS comorbidity risks in PWH.

Indexed as

HIV-1AdultAnti-HIV AgentsBacterial Translocationbeta-GlucansBiomarkersCD4-CD8 RatioCross-Sectional StudiesDisease ProgressionFatty Acid-Binding ProteinsFemaleHIV InfectionsHumansInterleukin-22Interleukin-6Interleukin-8Anti-HIV Agentsbeta-GlucansBiomarkersCD14 protein, humanCXCL8 protein, humanFABP2 protein, humanFatty Acid-Binding ProteinsIL6 protein, humanInterleukin-22Interleukin-6Interleukin-8InterleukinsLipopolysaccharide ReceptorsLipopolysaccharidesPancreatitis-Associated ProteinsREG3A protein, humanTumor Necrosis Factor-alphagut damageHIVinflammationmicrobial translocationREG3α

Identifiers

PMID31504638
PMCPMC6910878
OpenAlexW2969786980

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.