Evidence map›Paper›PMID 16630021›Full record

ArticleImmunology2006

Interferon-alphabeta mediates partial control of early pulmonary Mycobacterium bovis bacillus Calmette-Guérin infection.

John Kuchtey, Scott A Fulton, Scott M Reba, Clifford V Harding, W Henry Boom

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Type I interferons in tuberculosis: Foe and occasionally friend.The Journal of experimental medicine · 2018
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Target control of complex networks.Nature communications · 2014
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

5 authors at 3 institutions in 2 countries.

John KuchteyInstitute of Pathology, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, Ohio 44106-4984, USA.
Scott A Fulton
Scott M Reba
Clifford V Harding
W Henry Boom
Office of Infectious Diseases · USTaipei Institute of Pathology · TWCase Western Reserve University · US

Funding

Regulation of macrophages by Mycobacterium tuberculosisR01AI034343 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI HARDING, CLIFFORD V · 1994 to 2017
$6.2M
MYCOBACTERIUM TUBERCULOSIS INFECTION IN THE LUNGR01HL055967 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI BOOM, W. HENRY · 1995 to 2010
$4.2M
CPG DNA ADJUVANTS AND VACCINES FOR ENCAPSULATED BACTERIAR01AI047255 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI HARDING, CLIFFORD V · 2000 to 2004
$1.4M
PULMONARY IMMUNE DEFENCES AGAINST M. BOVIS-BCG INFECTIONK08HL004299 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI FULTON, SCOTT A · 2000 to 2004
$631k
NHLBI NIH HHS HL55967NHLBI NIH HHS K08 HL004299NHLBI NIH HHS K8-HL04299NHLBI NIH HHS R01 HL055967NIAID NIH HHS AI34343NIAID NIH HHS AI47255NIAID NIH HHS R01 AI034343NIAID NIH HHS R01 AI047255
6 · The paper itself

Abstract

The role of type I interferon (IFN-alphabeta) in modulating innate or adaptive immune responses against mycobacterial infection in the lung is unclear. In this study we investigated the susceptibility of IFN-alphabeta-receptor-deficient (IFN-alphabetaR-/-) mice to pulmonary infection with aerosolized Mycobacterium bovis bacillus Calmette-Guérin (BCG). During early infection (2-3 weeks), enhanced growth of BCG was measured in the lungs of IFN-alphabetaR-/- mice compared to wild-type mice. However, during late infection the burden of BCG was similar in the lungs of IFN-alphabetaR-/- and wild-type mice. Although control of BCG growth was delayed, recruitment and activation of T and natural killer cells, production of IFN-gamma, and cytokine expression were all similar in wild-type and IFN-alphabetaR-/- mice. However, decreased expression of nitric oxide in bronchoalveolar lavage fluids from IFN-alphabetaR-/- mice correlated with enhanced growth of BCG. Bone marrow-derived macrophages from IFN-alphabetaR-/- mice also produced less nitric oxide following infection with BCG in vitro. These findings suggest that IFN-alphabeta contributes to innate immunity to pulmonary mycobacterial infection by augmenting production of nitric oxide.

Indexed as

Mycobacterium bovisAnimalsBronchoalveolar Lavage FluidCells, CulturedFemaleImmunity, InnateInterferon-gammaKiller Cells, NaturalLungLymphocyte ActivationMacrophagesMaleMembrane ProteinsMiceMice, KnockoutNitric OxideInterferon-gammaMembrane ProteinsNitric OxideReceptor, Interferon alpha-betaReceptors, Interferon

Identifiers

PMID16630021
PMCPMC1782276
OpenAlexW2114257703

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.