Evidence map›Paper›PMID 27428431›Full record

ArticleEBioMedicine2016

Gut Bacteria Metabolism Impacts Immune Recovery in HIV-infected Individuals.

Sergio Serrano-Villar, David Rojo, Mónica Martínez-Martínez, Simon Deusch, Jorge F Vázquez-Castellanos, Rafael Bargiela, Talía Sainz, Mar Vera, Santiago Moreno, Vicente Estrada and 6 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

67 citing papers in PubMed, 111 citations in OpenAlex.

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7 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

16 authors at 8 institutions in 2 countries.

Sergio Serrano-VillarDepartment of Infectious Diseases, University Hospital Ramón y Cajal and Ramón y Cajal Health Research Institute (IRYCIS), Madrid, Spain.
David RojoCentro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad CEU San Pablo, Campus Montepríncipe, Madrid, Spain.
Mónica Martínez-MartínezInstitute of Catalysis, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Simon DeuschInstitute of Animal Science, Universität Hohenheim, Stuttgart, Germany.
Jorge F Vázquez-CastellanosFoundation for the Promotion of Health and Biomedical Research in the Valencian Community (FISABIO) - Public Health, Valencia, Spain; Network Research Center for Epidemiology and Public Health (CIBER-ESP), Madrid, Spain.
Rafael BargielaInstitute of Catalysis, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Talía SainzDepartment of Pediatric Infectious Diseases, University Hospital La Paz, and La Paz Research Institute (IdiPAZ), Madrid, Spain.
Mar VeraCentro Sanitario Sandoval, Madrid, Spain.
Santiago MorenoDepartment of Infectious Diseases, University Hospital Ramón y Cajal and Ramón y Cajal Health Research Institute (IRYCIS), Madrid, Spain.
Vicente EstradaHIV Unit, Department of Internal Medicine, University Hospital Clínico San Carlos, Madrid, Spain.
María José GosalbesFoundation for the Promotion of Health and Biomedical Research in the Valencian Community (FISABIO) - Public Health, Valencia, Spain; Network Research Center for Epidemiology and Public Health (CIBER-ESP), Madrid, Spain.
Amparo LatorreFoundation for the Promotion of Health and Biomedical Research in the Valencian Community (FISABIO) - Public Health, Valencia, Spain; Network Research Center for Epidemiology and Public Health (CIBER-ESP), Madrid, Spain; Instituto Cavanilles de Biodiversidad y Biología Evolutiva (Universidad de Valencia), Valencia, Spain.
Jana SeifertInstitute of Animal Science, Universität Hohenheim, Stuttgart, Germany.
Coral BarbasCentro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad CEU San Pablo, Campus Montepríncipe, Madrid, Spain. Electronic address: cbarbas@ceu.es.
Andrés MoyaFoundation for the Promotion of Health and Biomedical Research in the Valencian Community (FISABIO) - Public Health, Valencia, Spain; Network Research Center for Epidemiology and Public Health (CIBER-ESP), Madrid, Spain; Instituto Cavanilles de Biodiversidad y Biología Evolutiva (Universidad de Valencia), Valencia, Spain. Electronic address: andres.moya@uv.es.
Manuel FerrerInstitute of Catalysis, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain. Electronic address: mferrer@icp.csic.es.
Consejo Superior de Investigaciones Científicas · ESFundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana · ESInstituto Cajal · ESUniversidad San Pablo CEU · ESUniversitat de València · ESUniversity of Hohenheim · DEHospital Clínico San Carlos · ESHospital La Paz Institute for Health Research · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While changes in gut microbial populations have been described in human immuno-deficiency virus (HIV)-infected patients undergoing antiretroviral therapy (ART), the mechanisms underlying the contributions of gut bacteria and their molecular agents (metabolites and proteins) to immune recovery remain unexplored. To study this, we examined the active fraction of the gut microbiome, through examining protein synthesis and accumulation of metabolites inside gut bacteria and in the bloodstream, in 8 healthy controls and 29 HIV-infected individuals (6 being longitudinally studied). We found that HIV infection is associated to dramatic changes in the active set of gut bacteria simultaneously altering the metabolic outcomes. Effects were accentuated among immunological ART responders, regardless diet, subject characteristics, clinical variables other than immune recovery, the duration and type of ART and sexual preferences. The effect was found at quantitative levels of several molecular agents and active bacteria which were herein identified and whose abundance correlated with HIV immune pathogenesis markers. Although, we cannot rule out the possibility that some changes are partially a random consequence of the disease status, our data suggest that most likely reduced inflammation and immune recovery is a joint solution orchestrated by both the active fraction of the gut microbiota and the host.

Indexed as

Gastrointestinal MicrobiomeHIV-1Antiretroviral Therapy, Highly ActiveBacteriaBiomarkersCase-Control StudiesCD4 Lymphocyte CountFemaleHIV InfectionsHumansImmunityMaleMetabolomeMetabolomicsViral LoadBiomarkersAntiretroviral therapyGut microbiotaHIVImmune recoveryMetabolomeMetaproteome

Identifiers

PMID27428431
PMCPMC4919658
OpenAlexW2345060140

What OpenQuestion holds

Textmetadata
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.