Evidence map›Paper›PMID 28125732›Full record

ArticlePLoS pathogens2017

Dysregulation of Systemic and Mucosal Humoral Responses to Microbial and Food Antigens as a Factor Contributing to Microbial Translocation and Chronic Inflammation in HIV-1 Infection.

Zdenek Hel, Jun Xu, Warren L Denning, E Scott Helton, Richard P H Huijbregts, Sonya L Heath, E Turner Overton, Benjamin S Christmann, Charles O Elson, Paul A Goepfert and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 23 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

11 authors at 3 institutions in 2 countries.

Zdenek HelDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Jun XuDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Warren L DenningDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
E Scott HeltonDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID 0000-0002-9954-8222
Richard P H HuijbregtsDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Sonya L HeathDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
E Turner OvertonDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Benjamin S ChristmannDepartment of Natural Science and Mathematics, Lee University, Cleveland, Tennessee, United States of America.ORCID 0000-0002-2478-5581
Charles O ElsonDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Paul A GoepfertDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Jiri MesteckyDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
University of Alabama at Birmingham · USCharles University · CZLee University · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OLAF KUTSCH · 1988 to 2026
$84.1M
IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
EXTRAMURAL RESEARCH FACILITIES IMPROVEMENT: PHYSIOLOGYC06RR020136 · NCRR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MARCHASE, RICHARD BANFIELD · 2004 to 2004
$3.6M
Dysregulation of IgA responses in HIV-1-infected individualsR01AI074438 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HEL, ZDENEK · 2007 to 2011
$2.4M
Neutrophil dysregulation as a driving mechanism of cardiovascular disease in HIV-1-infectionR01HL129878 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HEL, ZDENEK · 2016 to 2019
$2.3M
The Guts of HIV: Innate Immune Dysregulation as a Central Mechanism of Gastrointestinal and Liver Disease in HIV-1-infected IndividualsR01DK108353 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HEL, ZDENEK · 2015 to 2019
$1.6M
Neutrophil-mediated immune suppression as a mechanism of HIV-1 pathogenesis.R21AI104458 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HEL, ZDENEK · 2013 to 2014
$404k
NCI NIH HHS P30 CA013148NCRR NIH HHS C06 RR020136NHLBI NIH HHS R01 HL129878NIAID NIH HHS P30 AI027767NIAID NIH HHS R01 AI074438NIAID NIH HHS R21 AI104458NIAID NIH HHS T32 AI007051NIDDK NIH HHS R01 DK108353
6 · The paper itself

Abstract

HIV-1 infection is associated with an early and profound depletion of mucosal memory CD4+ T cells, a population that plays an indispensable role in the regulation of isotype switching and transepithelial transport of antibodies. In this study, we addressed whether the depletion of CD4+ T cell in HIV-1-infected individuals results in altered humoral responses specific to antigens encountered at mucosal surfaces. Comprehensive protein microarray of systemic humoral responses to intestinal microbiota demonstrated reduced IgG responses to antigens derived from Proteobacteria and Firmicutes but not Bacteroidetes. Importantly, intestinal secretions of antiretroviral therapy-treated HIV-1-infected individuals exhibited a significant elevation of IgM levels and decreased IgA/IgM and IgG/IgM ratios of antibodies specific to a variety of microbial and food antigens. The presented findings indicate reduced competence of mucosal B cells for class switch recombination from IgM to other isotypes limiting their capacity to react to changing antigenic variety in the gut lumen. Decreased availability of microbiota-specific IgA and IgG may be an important factor contributing to the translocation of microbial antigens across the intestinal mucosal barrier and their systemic dissemination that drives chronic inflammation in HIV-1-infected individuals.

Indexed as

AntigensB-LymphocytesCD4-Positive T-LymphocytesChronic DiseaseFoodGene Expression RegulationHIV-1HIV InfectionsHumansImmunity, HumoralImmunoglobulin AImmunoglobulin Class SwitchingImmunoglobulin GInflammationIntestinal MucosaMicrobiotaAntigensImmunoglobulin AImmunoglobulin G

Identifiers

PMID28125732
PMCPMC5268400
OpenAlexW2582285546

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.