Evidence map›Paper›PMID 26471500›Full record

ArticleEuropean journal of immunology2016

Tissue factor expression by myeloid cells contributes to protective immune response against Mycobacterium tuberculosis infection.

Sambasivan Venkatasubramanian, Deepak Tripathi, Torry Tucker, Padmaja Paidipally, Satyanarayana Cheekatla, Elwyn Welch, Anjana Raghunath, Ann Jeffers, Amy R Tvinnereim, Melissa E Schechter and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Observational
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The coagulation system in host defense.Research and practice in thrombosis and haemostasis · 2018
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. The involvement of endothelial mediators in leprosy.Memorias do Instituto Oswaldo Cruz · 2016
    Article
  14. Article
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

14 authors at 4 institutions in 2 countries.

Sambasivan VenkatasubramanianDepartment of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Deepak TripathiDepartment of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Torry TuckerDepartment of Cellular and Molecular Biology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Padmaja PaidipallyDepartment of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Satyanarayana CheekatlaDepartment of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Elwyn WelchDepartment of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Anjana RaghunathDepartment of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Ann JeffersDepartment of Cellular and Molecular Biology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Amy R TvinnereimDepartment of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Melissa E SchechterClinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Bruno B AndradeInvestigative Medicine Branch, Laboratory of Immune Regulation, Centro de Pesquisas Gonçalo Moniz (CPqGM), Fundação Oswaldo Cruz (FIOCRUZ), Salvador, Bahia, Brazil.
Nizel MackmanDepartment of Medicine, The University of North Carolina at Chapel Hill School of Medicine, NC, USA.
Steven IdellDepartment of Cellular and Molecular Biology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
Ramakrishna VankayalapatiDepartment of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, TX, USA.
The University of Texas Health Science Center at Tyler · USFrederick National Laboratory for Cancer Research · USFundação Oswaldo Cruz · BRUniversity of North Carolina at Chapel Hill · US

Funding

The role of NK cells in human M. Tuberculosis infectionR01AI054629 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI VANKAYALAPATI, RAMAKRISHNA · 2005 to 2009
$1.3M
The role of coagulation cascade proteases in pleural fibrosisK01HL115466 · NHLBI · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI TUCKER, TORRY ALLE · 2012 to 2016
$551k
The role of NK cells in HIV and tuberculosis co-infectionR21AI094692 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI VANKAYALAPATI, RAMAKRISHNA · 2011 to 2012
$383k
The role of regulatory T cells in M. tuberculosis infectionR21AI073612 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI VANKAYALAPATI, RAMAKRISHNA · 2008 to 2009
$369k
The mechanisms of regulatory T-cell expansion in human Mycobacterium tuberculosisR56AI085135 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI VANKAYALAPATI, RAMAKRISHNA · 2010 to 2010
$353k
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENHLBI NIH HHS K01 HL115466NIAID NIH HHS AI085135NIAID NIH HHS AI094692NIAID NIH HHS R01 AI054629NIAID NIH HHS R21 AI073612NIAID NIH HHS R21 AI094692NIAID NIH HHS R56 AI085135
6 · The paper itself

Abstract

Tissue factor (TF) is a transmembrane glycoprotein that plays an essential role in hemostasis by activating coagulation. TF is also expressed by monocytes/macrophages as part of the innate immune response to infections. In the current study, we determined the role of TF expressed by myeloid cells during Mycobacterium tuberculosis (M. tb) infection by using mice lacking the TF gene in myeloid cells (TF(Δ) ) and human monocyte derived macrophages (MDMs). We found that during M. tb infection, a deficiency of TF in myeloid cells was associated with reduced inducible nitric oxide synthase (iNOS) expression, enhanced arginase 1 (Arg1) expression, enhanced IL-10 production and reduced apoptosis in infected macrophages, which augmented M. tb growth. Our results demonstrate that a deficiency of TF in myeloid cells promotes M2-like phenotype in M .tb infected macrophages. A deficiency in TF expression by myeloid cells was also associated with reduced fibrin deposition and increased matrix metalloproteases (MMP)-2 and MMP-9 mediated inflammation in M. tb infected lungs. Our studies demonstrate that TF expressed by myeloid cells has newly recognized abilities to polarize macrophages and to regulate M. tb growth.

Indexed as

AnimalsBacteremiaBlood CoagulationCell DifferentiationFemaleFibrinHost-Pathogen InteractionsHumansImmunity, InnateLungMacrophagesMice, Inbred C57BLMice, KnockoutMycobacterium tuberculosisPneumoniaThromboplastinFibrinThromboplastinApoptosisIL-10MacrophageM. tuberculosisTissue factor

Identifiers

PMID26471500
PMCPMC4740218
OpenAlexW1951935305

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.