Evidence map›Paper›PMID 25676469›Full record

ArticleThe Journal of infectious diseases2015

The Extracellular Matrix Regulates Granuloma Necrosis in Tuberculosis.

Basim Al Shammari, Takayuki Shiomi, Liku Tezera, Magdalena K Bielecka, Victoria Workman, Tarangini Sathyamoorthy, Francesco Mauri, Suwan N Jayasinghe, Brian D Robertson, Jeanine D'Armiento and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
9.1field-weighted citation impact, top 1% 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

65 citing papers in PubMed, 103 citations in OpenAlex.

  1. Trial
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  3. Applications of humanized mice inMolecular medicine reports · 2026
    Review
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  19. CWHM-12, an Antagonist of Integrin-Mediated Transforming Growth Factor-Beta Activation Confers Protection During EarlyJournal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2022
    Article
  20. Liposomal Glutathione Helps to MitigateAntioxidants (Basel, Switzerland) · 2022
    Article

5 more citing papers are in PubMed but not listed here.

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

12 authors at 6 institutions in 4 countries.

Basim Al ShammariInfectious Diseases and Immunity Section, Division of Infectious Diseases.
Takayuki ShiomiDepartment of Medicine, Columbia University, New York, New York.
Liku TezeraNIHR Respiratory Biomedical Research Unit, Clinical and Experimental Sciences Academic Unit, Faculty of Medicine.
Magdalena K BieleckaNIHR Respiratory Biomedical Research Unit, Clinical and Experimental Sciences Academic Unit, Faculty of Medicine.
Victoria WorkmanBioPhysics Group, Department of Mechanical Engineering Institute of Biomedical Engineering Centre for Stem Cells and Regenerative Medicine, University College London.
Tarangini SathyamoorthyInfectious Diseases and Immunity Section, Division of Infectious Diseases.
Francesco MauriHistopathology Department, Centre for Pathology, Division of Experimental Medicine.
Suwan N JayasingheBioPhysics Group, Department of Mechanical Engineering Institute of Biomedical Engineering Centre for Stem Cells and Regenerative Medicine, University College London.
Brian D RobertsonMRC Centre for Molecular Bacteriology and Infection, Department of Medicine, Imperial College London.
Jeanine D'ArmientoDepartment of Medicine, Columbia University, New York, New York.
Jon S FriedlandInfectious Diseases and Immunity Section, Division of Infectious Diseases.
Paul T ElkingtonInfectious Diseases and Immunity Section, Division of Infectious Diseases NIHR Respiratory Biomedical Research Unit, Clinical and Experimental Sciences Academic Unit, Faculty of Medicine Institute for Life Sciences, University of Southampton, United Kingdom.
Office of Infectious Diseases · USColumbia University · USCentre of Experimental Medicine of the Slovak Academy of Sciences · SKImperial College London · GBInstitute for Stem Cell Biology and Regenerative Medicine · INUniversity College London · GB

Funding

Targeting matrix metalloproteinases to limit immunopathology in airborne infectioR33AI102239 · NIAID · UNIVERSITY OF SOUTHAMPTON · PI ELKINGTON, PAUL TIMOTHY · 2014 to 2016
$1.1M
Targeting matrix metalloproteinases to limit immunopathology in airborne infectioR21AI102239 · NIAID · UNIVERSITY OF SOUTHAMPTON · PI D'ARMIENTO, JEANINE M, ELKINGTON, PAUL TIMOTHY · 2012 to 2013
$289k
Medical Research Council MR/J006874/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/L001039/1NIAID NIH HHS AI102239NIAID NIH HHS R21 AI102239NIAID NIH HHS R33 AI102239
6 · The paper itself

Abstract

A central tenet of tuberculosis pathogenesis is that caseous necrosis leads to extracellular matrix destruction and bacterial transmission. We reconsider the underlying mechanism of tuberculosis pathology and demonstrate that collagen destruction may be a critical initial event, causing caseous necrosis as opposed to resulting from it. In human tuberculosis granulomas, regions of extracellular matrix destruction map to areas of caseous necrosis. In mice, transgenic expression of human matrix metalloproteinase 1 causes caseous necrosis, the pathological hallmark of human tuberculosis. Collagen destruction is the principal pathological difference between humanised mice and wild-type mice with tuberculosis, whereas the release of proinflammatory cytokines does not differ, demonstrating that collagen breakdown may lead to cell death and caseation. To investigate this hypothesis, we developed a 3-dimensional cell culture model of tuberculosis granuloma formation, using bioelectrospray technology. Collagen improved survival of Mycobacterium tuberculosis-infected cells analyzed on the basis of a lactate dehydrogenase release assay, propidium iodide staining, and measurement of the total number of viable cells. Taken together, these findings suggest that collagen destruction is an initial event in tuberculosis immunopathology, leading to caseous necrosis and compromising the immune response, revealing a previously unappreciated role for the extracellular matrix in regulating the host-pathogen interaction.

Indexed as

AnimalsCollagenExtracellular MatrixGranulomaHost-Pathogen InteractionsHumansLungLung NeoplasmsMatrix Metalloproteinase 1MiceMice, Inbred C57BLMice, TransgenicModels, BiologicalNecrosisTuberculosisCollagenMatrix Metalloproteinase 1MMP1 protein, humanextracellular matriximmunopathologymatrix metalloproteasetuberculosis

Identifiers

PMID25676469
PMCPMC4539912
OpenAlexW1965899093

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.