Evidence map›Paper›PMID 26603204›Full record

ArticleThe Journal of infectious diseases2016

Toll-like Receptor 4 Signaling on Dendritic Cells Suppresses Polymorphonuclear Leukocyte CXCR2 Expression and Trafficking via Interleukin 10 During Intra-abdominal Sepsis.

Meihong Deng, Tao Ma, Zhengzheng Yan, Kent R Zettel, Melanie J Scott, Hong Liao, Alicia Frank, Adrian E Morelli, Chhinder P Sodhi, David J Hackam and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. A narrative review of chemokine receptors CXCR1 and CXCR2 and their role in acute respiratory distress syndrome.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
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  9. Review
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  14. cGAS-mediated autophagy protects the liver from ischemia-reperfusion injury independently of STING.American journal of physiology. Gastrointestinal and liver physiology · 2018
    Article
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  18. Review
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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 4 institutions in 2 countries.

Meihong DengDepartment of Surgery, University of Pittsburgh, Pennsylvania.
Tao MaDepartment of General Surgery, Tianjin Medical University General Hospital.
Zhengzheng YanDepartment of Pathophysiology, Southern Medical University, Guangzhou, China.
Kent R ZettelDepartment of Surgery, University of Pittsburgh, Pennsylvania.
Melanie J ScottDepartment of Surgery, University of Pittsburgh, Pennsylvania.
Hong LiaoDepartment of Surgery, University of Pittsburgh, Pennsylvania.
Alicia FrankDepartment of Surgery, University of Pittsburgh, Pennsylvania.
Adrian E MorelliDepartment of Surgery, University of Pittsburgh, Pennsylvania.
Chhinder P SodhiJohns Hopkins Children's Center, Baltimore, Maryland.
David J HackamJohns Hopkins Children's Center, Baltimore, Maryland.
Timothy R BilliarDepartment of Surgery, University of Pittsburgh, Pennsylvania.
University of Pittsburgh · USJohns Hopkins University · USSouthern Medical University · CNTianjin Medical University General Hospital · CN

Funding

Regulation and Function of Endotoxin Signaling in Surgical SepsisR01GM050441 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BILLIAR, TIMOTHY R · 1994 to 2018
$4.6M
TLR4 Signaling in the Pathogenesis of Surgical Necrotizing EnterocolitisR01GM078238 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HACKAM, DAVID J · 2006 to 2019
$3.9M
Modulation of TLR4 and TLR9 Signaling in NECR01DK083752 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HACKAM, DAVID J · 2008 to 2016
$3.4M
NIDDK NIH HHS R01 DK083752NIGMS NIH HHS R01 GM050441NIGMS NIH HHS R01-GM-050441NIGMS NIH HHS R01 GM078238
6 · The paper itself

Abstract

backgroundToll-like receptor 4 (TLR4) is a critical receptor involved in the sensing of gram-negative bacterial infection. However, the roles of TLR4 in sepsis are cell-type specific. Dendritic cells (DCs) are known to play a central role in microbial detection, alerting the immune system to the presence of infection and coordinating adaptive immune response. The goal of this study was to investigate the impact of DC-specific TLR4 signaling on host defense against intra-abdominal polymicrobial sepsis.

methodsC57BL/6, global Tlr4 knockout, cell-specific knockout control, and CD11c-specific Tlr4(-/-) mice underwent cecal ligation and puncture (CLP).

resultsSpecific deletion of TLR4 on DCs in mice improved survival and enhanced bacterial clearance. Deletion of TLR4 on DCs was associated with lower levels of circulating interleukin 10 (IL-10), higher polymorphonuclear leukocyte (PMN) accumulation in the peritoneal cavity, and higher expression of chemokine (C-X-C motif) receptor 2 (CXCR2) on PMNs after CLP. In vitro studies of DC and neutrophil cocultures confirmed that TLR4-dependent secretion of IL-10 from DCs regulated neutrophil CXCR2 expression.

conclusionsOur data shed light on a previously unrecognized role for TLR4 signaling on DCs in driving IL-10 secretion during sepsis and, through this pathway, regulates PMN recruitment via suppression of CXCR2 expression.

Indexed as

AnimalsDendritic CellsDisease Models, AnimalInterleukin-10Intraabdominal InfectionsMaleMiceMice, Inbred C57BLReceptors, Interleukin-8BSepsisToll-Like Receptor 4Interleukin-10Receptors, Interleukin-8BToll-Like Receptor 4CLPCXCR2dendritic cellIL-10PMN recruitmentsepsisTLR4

Identifiers

PMID26603204
PMCPMC4799664
OpenAlexW2302164906

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.