Evidence map›Paper›PMID 19007905›Full record

ArticleMicrobes and infection2009

Trehalose 6,6'-dimycolate on the surface of Mycobacterium tuberculosis modulates surface marker expression for antigen presentation and costimulation in murine macrophages.

Celestine Kan-Sutton, Chinnaswamy Jagannath, Robert L Hunter

Open access · greenAbstract read
In one paragraph

Article in Microbes and infection, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

22 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  5. Review
  6. Generation of Liposomes to Study the Effect ofInternational journal of molecular sciences · 2021
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. RecombinantExperimental and therapeutic medicine · 2017
    Article
  12. Macrophages in tuberculosis: friend or foe.Seminars in immunopathology · 2013
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review
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

3 authors at 2 institutions in 1 country.

Celestine Kan-SuttonDepartment of Pathology and Laboratory Medicine, The University of Texas at Houston Health Science Center, 6431 Fannin Street, Houston, TX 77030, USA. celestine.kan@uth.tmc.edu
Chinnaswamy Jagannath
Robert L Hunter
The University of Texas Health Science Center at Houston · USThe University of Texas Health Science Center · US

Funding

Genetic Control of Pulmonary Cavities in TuberculosisR01HL068537 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HUNTER, ROBERT L. · 2001 to 2005
$2.2M
NHLBI NIH HHS R01 HL068537
6 · The paper itself

Abstract

Trehalose 6,6'-dimycolate (TDM) is the most abundant lipid extracted from Mycobacterium tuberculosis (MTB). TDM promotes MTB survival by decreasing phagosomal acidification and phagolysosomal fusion in macrophages. Delipidation of MTB using petroleum ether removes TDM and decreases MTB survival within host cells. TDM reconstituted onto MTB restores its virulent wild-type characteristics. We investigated the role of TDM in regulating surface marker expression in MTB-infected macrophages. Macrophages were infected with wild-type, delipidated, and TDM-reconstituted MTB for 24h and measured for changes in surface marker expression. TDM on MTB was found to specifically target MHCII, CD1d, CD40, CD80 and CD86. Both wild-type and TDM-reconstituted MTB suppressed or induced no change in expression of these surface markers, whereas delipidated MTB increased expression of the same markers. MTB-infected macrophages were also overlaid with MHCII-restricted T cell hybridomas which recognize Antigen 85B. Macrophages infected by wild-type and TDM-reconstituted MTB did not present antigen as well as delipidated MTB-infected macrophages. The evidence shown furthers supports the notion that TDM present on MTB promotes its survival and persistence in host macrophages.

Indexed as

Antigen PresentationMacrophages, AlveolarMacrophages, PeritonealAcyltransferasesAnimalsAntigens, BacterialAntigens, SurfaceBacterial ProteinsCell Line, TransformedCord FactorsMiceMice, Inbred C57BLMycobacterium tuberculosisSuppressor of Cytokine Signaling 1 ProteinSuppressor of Cytokine Signaling ProteinsAcyltransferasesantigen 85B, Mycobacterium tuberculosisAntigens, BacterialAntigens, SurfaceBacterial ProteinsCord FactorsSocs1 protein, mouseSuppressor of Cytokine Signaling 1 ProteinSuppressor of Cytokine Signaling Proteins

Identifiers

PMID19007905
PMCPMC2680729
OpenAlexW2081325298

What OpenQuestion holds

Textmetadata
LicenceTDM
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.