Evidence map›Paper›PMID 26364992›Full record

ArticleCytokine2015

The association between the Th-17 immune response and pulmonary complications in a trauma ICU population.

Travis L Holloway, Meenakshi Rani, Andrew P Cap, Ronald M Stewart, Martin G Schwacha

Abstract read
In one paragraph

Article in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Cellular and molecular mechanisms of Notch signal in pulmonary microvascular endothelial cells after acute lung injury.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2023
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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

5 authors at 2 institutions in 1 country.

Travis L HollowayDepartment of Surgery, The University of Texas Health Science Center at San Antonio, TX 78229, United States.
Meenakshi RaniDepartment of Surgery, The University of Texas Health Science Center at San Antonio, TX 78229, United States.
Andrew P CapUS Army Institute of Surgical Research, Fort Sam Houston, TX 78234, United States.
Ronald M StewartDepartment of Surgery, The University of Texas Health Science Center at San Antonio, TX 78229, United States.
Martin G SchwachaDepartment of Surgery, The University of Texas Health Science Center at San Antonio, TX 78229, United States; US Army Institute of Surgical Research, Fort Sam Houston, TX 78234, United States. Electronic address: schwacha@uthscsa.edu.
The University of Texas Health Science Center at San Antonio · USUnited States Army Institute of Surgical Research · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
INSTITUTE FOR INTEGRATION OF MEDICINE & SCIENCE: A PARTNERSHIP TO IMPROVE HEALTHUL1RR025767 · NCRR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A · 2008 to 2011
$23.8M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
Injury, Ischemia and Inflammation: A Translational Approach to Trauma TreatmentT32GM079085 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SCHWACHA, MARTIN G · 2008 to 2012
$396k
NCATS NIH HHS UL1 TR001120NCI NIH HHS P30 CA054174NCI NIH HHS P30 CA54174NCRR NIH HHS UL1 RR025767NCRR NIH HHS UL1RR025767NIGMS NIH HHS 5T32GM079085NIGMS NIH HHS T32 GM079085PHS HHS NIH/NCRR UL 1RR025767
6 · The paper itself

Abstract

backgroundThe overall immunopathology of the T-helper cell (Th)-17 immune response has been implicated in various inflammatory diseases including pulmonary inflammation; however its potential role in acute respiratory distress syndrome (ARDS) is not defined. This study aimed to evaluate the Th-17 response in bronchoalveolar lavage fluid (BALF) and blood and from trauma patients with pulmonary complications.

methodsA total of 21 severely injured intensive care unit (ICU) subjects, who were mechanically ventilated and undergoing bronchoscopy, were enrolled. BALF and blood were collected and analyzed for Th-1 (interferon [IFN]γ), Th-2 (interleukin [IL]-4, -10), Th-17 (IL-17A, -17F, -22, 23) and pro-inflammatory (IL-1β, IL-6, tumor necrosis factor [TNF]α) cytokine levels.

resultsSignificant levels of the Th-17 cytokines IL-17A, -17F and -21 and IL-6 (which can be classified as a Th-17 cytokine) were observed in the BALF of all subjects. There were no significant differences in Th-17 cytokines between those subjects with ARDS and those without, with the exception of plasma and BALF IL-6, which was markedly greater in ARDS subjects, as compared with controls and non-ARDS subjects.

conclusionsTrauma patients with pulmonary complications exhibited a significant Th-17 response in the lung and blood, suggesting that this pro-inflammatory milieu may be a contributing factor to such complications.

Indexed as

Intensive Care UnitsAdultBronchoalveolar Lavage FluidCase-Control StudiesCytokinesFemaleHumansMaleMiddle AgedProspective StudiesRespiratory Distress SyndromeTh17 CellsWounds and InjuriesYoung AdultCytokinesAcute lung injuryAcute respiratory distress syndromeIL-17InflammationInjury

Identifiers

PMID26364992
PMCPMC4632975
OpenAlexW1825832965

What OpenQuestion holds

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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.