Evidence map›Paper›PMID 17942369›Full record

ArticleTuberculosis (Edinburgh, Scotland)2008

Increased expression of host iron-binding proteins precedes iron accumulation and calcification of primary lung lesions in experimental tuberculosis in the guinea pig.

Randall J Basaraba, Helle Bielefeldt-Ohmann, Ellie K Eschelbach, Claire Reisenhauer, Airn E Tolnay, Lauren C Taraba, Crystal A Shanley, Erin A Smith, Cathy L Bedwell, Elizabeth A Chlipala and 1 more

Open access · greenAbstract read
In one paragraph

Article in Tuberculosis (Edinburgh, Scotland), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Functions and importance of mycobacterial extracellular vesicles.Applied microbiology and biotechnology · 2016
    Review
  9. Article
  10. Article
  11. Animal models of tuberculosis: Guinea pigs.Cold Spring Harbor perspectives in medicine · 2014
    Review
  12. Article
  13. Article
  14. Tuberculosis vaccine with high predicted population coverage and compatibility with modern diagnostics.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  15. A new unifying theory of the pathogenesis of tuberculosis.Tuberculosis (Edinburgh, Scotland) · 2014
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

11 authors at 2 institutions in 1 country.

Randall J BasarabaDepartment of Microbiology, Immunology and Pathology, 1619 Campus Delivery, Colorado State University, Fort Collins, CO 80523-1619, USA. basaraba@colostate.edu
Helle Bielefeldt-Ohmann
Ellie K Eschelbach
Claire Reisenhauer
Airn E Tolnay
Lauren C Taraba
Crystal A Shanley
Erin A Smith
Cathy L Bedwell
Elizabeth A Chlipala
Ian M Orme
Colorado State University · USPremier Research Group · US

Funding

Guinea pig model for TB vaccine evaluationsR01AI054697 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI ORME, IAN M · 2003 to 2007
$3.0M
NIAID NIH HHS AI054697NIAID NIH HHS R01 AI054697
6 · The paper itself

Abstract

The growth and virulence of Mycobacterium tuberculosis depends on its ability to scavenge host iron, an essential and limited micronutrient in vivo. In this study, we show that ferric iron accumulates both intra- and extra-cellularly in the primary lung lesions of guinea pigs aerosol-infected with the H37Rv strain of M. tuberculosis. Iron accumulated within macrophages at the periphery of the primary granulomatous lesions while extra-cellular ferric iron was concentrated in areas of lesion necrosis. Accumulation of iron within primary lesions was preceded by an increase in expression of heavy chain (H) ferritin, lactoferrin and receptors for transferrin, primarily by macrophages and granulocytes. The increased expression of intra-cellular H ferritin and extra-cellular lactoferrin, more so than transferrin receptor, paralleled the development of necrosis within primary lesions. The deposition of extra-cellular ferric iron within necrotic foci coincided with the accumulation of calcium and phosphorus and other cations in the form of dystrophic calcification. Primary lung lesions from guinea pigs vaccinated with Mycobactrium bovis BCG prior to experimental infection, had reduced iron accumulation as well as H ferritin, lactoferrin and transferrin receptor expression. The amelioration of primary lesion necrosis and dystrophic calcification by BCG vaccination was coincident with the lack of extra-cellular ferric iron and lactoferrin accumulation. These data demonstrate that BCG vaccination ameliorates primary lesion necrosis, dystrophic mineralization and iron accumulation, in part by down-regulating the expression of macrophage H ferritin, lactoferrin and transferrin receptors, in vivo.

Indexed as

AnimalsBCG VaccineCalcinosisCalciumFerritinsGuinea PigsImmunohistochemistryIron-Binding ProteinsLungMycobacterium tuberculosisTuberculosis, PulmonaryBCG VaccineCalciumFerritinsIron-Binding Proteins

Identifiers

PMID17942369
PMCPMC2271031
OpenAlexW2045132083

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.