Evidence map›Paper›PMID 23743311›Full record

ArticleThe international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease2013

Elevated IP-10 and IL-6 from bronchoalveolar lavage cells are biomarkers of non-cavitary tuberculosis.

A Nolan, R Condos, M L Huie, R Dawson, K Dheda, E Bateman, W N Rom, M D Weiden

Abstract read
In one paragraph

Article in The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease, 2013. 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
1.6field-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

16 citing papers in PubMed, 24 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

8 authors at 3 institutions in 2 countries.

A NolanDivision of Pulmonary, Critical Care, and Sleep Medicine, New York University School of Medicine, New York, NY 10016, USA.
R Condos
M L Huie
R Dawson
K Dheda
E Bateman
W N Rom
M D Weiden
New York University · USGroote Schuur Hospital · ZAUniversity of Cape Town · ZA

Funding

Longtitudinal Studies of HIV-Associated Bacterial PneumoniaR01HL090316 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ROM, WILLIAM N · 2007 to 2013
$4.2M
CD80 and CD86 mediated innate immune response in sepsisK23HL084191 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NOLAN, ANNA · 2008 to 2013
$955k
NHLBI NIH HHS HL090316NHLBI NIH HHS K23 HL084191NHLBI NIH HHS K23HL084191NHLBI NIH HHS R01 HL090316PHS HHS K24A1080298
6 · The paper itself

Abstract

backgroundActive TB disease can destroy lung parenchyma leading to cavities. Immune responses that predispose or protect individuals from lung damage during TB are poorly defined.

objectiveTo sample lung immune cells and assay bronchoalveolar lavage (BAL) cell cytokine production.

designEnrolled subjects (n = 73) had bilateral infiltrates and underwent BAL.

resultsAll had sputum culture demonstrating Mycobacterium tuberculosis and 22/73 (30%) had cavities on their chest radiograph. Those with cavities at presentation had a higher percentage of polymorphonuclear neutrophils (PMN) in BAL as well as lower inducible protein (IP) 10 (P < 0.01) and interleukin (IL) 6 (P = 0.013) in BAL cell supernatants compared to those without cavities. There was no correlation between cavities and other BAL or serum cytokines. IP-10 was negatively associated with BAL PMN. IP-10 and IL-6 expression above median reduces the odds of cavities by 79% and 78% in logistic regression models. IP-10 and IL-6 clustered with interferon-gamma and tumour necrosis factor-alpha in a principal component analysis, while IL-4 clustered with PMN.

conclusionIncreasing IP-10 and IL-6 production by BAL cells is associated with non-cavitary TB in patients who present with radiographically advanced TB. IP-10 and IL-6 may reflect an effective T-helper 1 immune control pathway for TB, attenuating tuberculous lung destruction.

Indexed as

AdultBronchoalveolar Lavage FluidCase-Control StudiesChemokine CXCL10Cross-Sectional StudiesFemaleHumansInterleukin-6Logistic ModelsMaleMiddle AgedMycobacterium tuberculosisNeutrophilsPrincipal Component AnalysisRadiographySputumChemokine CXCL10CXCL10 protein, humanInterleukin-6

Identifiers

PMID23743311
PMCPMC4050635
OpenAlexW1964500804

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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.