Evidence map›Paper›PMID 23762096›Full record

ReviewClinical & developmental immunology2013

Immune vulnerability of infants to tuberculosis.

Koen Vanden Driessche, Alexander Persson, Ben J Marais, Pamela J Fink, Kevin B Urdahl

Open access · goldAbstract readReview
In one paragraph

Review in Clinical & developmental immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

43 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Prospective Exploratory Evaluation of Cepheid Xpert Mycobacterium tuberculosis Host Response Cartridge: A Focus on Adolescents and Young Adults.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Article
  11. Popularity of HIV self-tests may say more about the state of our primary care system than about the device itself.Canada communicable disease report = Releve des maladies transmissibles au Canada · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Maternal HIV infection drives altered placentalFrontiers in microbiology · 2023
    Article
  16. Review
  17. Multiple tuberculomas and cavitating pulmonary tuberculosis in an infant.Journal of family medicine and primary care · 2022
    Article
  18. Tuberculosis Exposure from a Healthcare Worker to Patients in a Neonatal Intensive Care Unit (NICU).The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2022
    Article
  19. Article
  20. Fatal SARS-CoV-2 andBMJ case reports · 2021
    Article
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 4 institutions in 4 countries.

Koen Vanden DriesscheCentre for Understanding and Preventing Infections in Children, Child & Family Research Institute, University of British Columbia, Vancouver, BC, Canada V5Z 4H4. koen.vandendriessche@cw.bc.ca
Alexander Persson
Ben J Marais
Pamela J Fink
Kevin B Urdahl
University of British Columbia · CACenter for Infectious Disease Research · USThe University of Sydney · AUUniversity of Washington · US

Funding

CHARACTERIZATION OF RECENT THYMIC EMIGRANTSR01AI064318 · NIAID · UNIVERSITY OF WASHINGTON · PI URDAHL, KEVIN B · 2005 to 2019
$5.8M
T regulatory cells and immunity in tuberculosisR01AI076327 · NIAID · UNIVERSITY OF WASHINGTON · PI URDAHL, KEVIN B · 2009 to 2018
$4.5M
NIAID NIH HHS R01 AI 064318NIAID NIH HHS R01 AI064318NIAID NIH HHS R01 AI076327NIAID NIH HHS R01AI 076327
6 · The paper itself

Abstract

One of the challenges faced by the infant immune system is learning to distinguish the myriad of foreign but nonthreatening antigens encountered from those expressed by true pathogens. This balance is reflected in the diminished production of proinflammatory cytokines by both innate and adaptive immune cells in the infant. A downside of this bias is that several factors critical for controlling Mycobacterium tuberculosis infection are significantly restricted in infants, including TNF, IL-1, and IL-12. Furthermore, infant T cells are inherently less capable of differentiating into IFN- γ -producing T cells. As a result, infected infants are 5-10 times more likely than adults to develop active tuberculosis (TB) and have higher rates of severe disseminated disease, including miliary TB and meningitis. Infant TB is a fundamentally different disease than TB in immune competent adults. Immunotherapeutics, therefore, should be specifically evaluated in infants before they are routinely employed to treat TB in this age group. Modalities aimed at reducing inflammation, which may be beneficial for adjunctive therapy of some forms of TB in older children and adults, may be of no benefit or even harmful in infants who manifest much less inflammatory disease.

Indexed as

Immunity, InnateAdultAge FactorsAntitubercular AgentsChildDisease SusceptibilityHumansImmunologic FactorsInfantInterferon-gammaInterleukin-1Interleukin-12Mycobacterium tuberculosisTuberculosisAntitubercular AgentsImmunologic FactorsInterferon-gammaInterleukin-1Interleukin-12

Identifiers

PMID23762096
PMCPMC3666431
OpenAlexW2125689304

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.