Evidence map›Paper›PMID 26109643›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Bacterial Membrane Vesicles Mediate the Release of Mycobacterium tuberculosis Lipoglycans and Lipoproteins from Infected Macrophages.

Jaffre J Athman, Ying Wang, David J McDonald, W Henry Boom, Clifford V Harding, Pamela A Wearsch

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

95 citing papers in PubMed, 136 citations in OpenAlex.

  1. Article
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  5. Deferoxamine Exhibits Antimicrobial and Immunomodulatory Activity AgainstInternational journal of molecular sciences · 2026
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  7. Article
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  9. Review
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  12. Article
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  14. Article
  15. Review
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  17. Article
  18. Review
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  20. Article

35 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

6 authors at 3 institutions in 1 country.

Jaffre J AthmanDepartment of Pathology, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH;
Ying WangDepartment of Pathology, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH;
David J McDonaldDepartment of Molecular Biology and Microbiology, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH; Center for AIDS Research, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH; and.
W Henry BoomCenter for AIDS Research, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH; and Division of Infectious Diseases, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH.
Clifford V HardingDepartment of Pathology, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH; Center for AIDS Research, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH; and.
Pamela A WearschDepartment of Pathology, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH; Center for AIDS Research, Case Western Reserve University/University Hospitals Case Medical Center, Cleveland, OH; and paw28@case.edu.
Case Western Reserve University · USUniversity Hospitals Case Medical Center · USUniversity Hospitals of Cleveland · US

Funding

WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Sharon L. Hillier, JONATHAN KARN · 1994 to 2026
$50.0M
GRADUATE TRAINING IN CELLULAR AND MOLECULAR BIOLOGYT32GM008056 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI DIEHL, JOHN ALAN, SNIDER, MARTIN D · 1985 to 2019
$7.1M
Regulation of macrophages by Mycobacterium tuberculosisR01AI034343 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI HARDING, CLIFFORD V · 1994 to 2017
$6.2M
HETEROGENEITY OF TCELLS IN M TUBERCULOSIS INFECTIONR01AI027243 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI BOOM, W. HENRY · 1989 to 2016
$5.5M
M. tuberculosis lipoprotein-TLR2 interactionsR01AI069085 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI HARDING, CLIFFORD V · 2007 to 2011
$1.9M
Roles for Exosomes in Adaptive Immunity to M. tuberculosisR21AI103443 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI WEARSCH, PAMELA A · 2013 to 2014
$435k
NIAID NIH HHS P30 AI036219NIAID NIH HHS R01 AI027243NIAID NIH HHS R01 AI034343NIAID NIH HHS R01 AI069085NIAID NIH HHS R21 AI103443NIGMS NIH HHS T32 GM008056
6 · The paper itself

Abstract

Mycobacterium tuberculosis is an intracellular pathogen that infects lung macrophages and releases microbial factors that regulate host defense. M. tuberculosis lipoproteins and lipoglycans block phagosome maturation, inhibit class II MHC Ag presentation, and modulate TLR2-dependent cytokine production, but the mechanisms for their release during infection are poorly defined. Furthermore, these molecules are thought to be incorporated into host membranes and released from infected macrophages within exosomes, 40-150-nm extracellular vesicles that derive from multivesicular endosomes. However, our studies revealed that extracellular vesicles released from infected macrophages include two distinct, largely nonoverlapping populations: one containing host cell markers of exosomes (CD9, CD63) and the other containing M. tuberculosis molecules (lipoglycans, lipoproteins). These vesicle populations are similar in size but have distinct densities, as determined by separation on sucrose gradients. Release of lipoglycans and lipoproteins from infected macrophages was dependent on bacterial viability, implicating active bacterial mechanisms in their secretion. Consistent with recent reports of extracellular vesicle production by bacteria (including M. tuberculosis), we propose that bacterial membrane vesicles are secreted by M. tuberculosis within infected macrophages and subsequently are released into the extracellular environment. Furthermore, extracellular vesicles released from M. tuberculosis-infected cells activate TLR2 and induce cytokine responses by uninfected macrophages. We demonstrate that these activities derive from the bacterial membrane vesicles rather than exosomes. Our findings suggest that bacterial membrane vesicles are the primary means by which M. tuberculosis exports lipoglycans and lipoproteins to impair effector functions of infected macrophages and circulate bacterial components beyond the site of infection to regulate immune responses by uninfected cells.

Indexed as

AnimalsCells, CulturedExosomesLipopolysaccharidesLipoproteinsLungMacrophages, AlveolarMiceMice, Inbred C57BLMycobacterium tuberculosisSecretory VesiclesToll-Like Receptor 2Tuberculosis, PulmonaryLipopolysaccharidesLipoproteinsTlr2 protein, mouseToll-Like Receptor 2

Identifiers

PMID26109643
PMCPMC4506856
OpenAlexW1489360290

What OpenQuestion holds

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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.