Evidence map›Paper›PMID 19037923›Full record

ArticleClinical and experimental immunology2008

Impaired dendritic cell maturation and cytokine production in patients with chronic mucocutanous candidiasis with or without APECED.

K R Ryan, M Hong, P D Arkwright, A R Gennery, C Costigan, M Dominguez, D Denning, V McConnell, A J Cant, M Abinun and 2 more

Abstract read
In one paragraph

Article in Clinical and experimental immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Trial
  2. Article
  3. Journal of fungi (Basel, Switzerland) · 2021
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Antifungal Th Immunity: Growing up in Family.Frontiers in immunology · 2014
    Review
  11. Human APECED; a Sick Thymus Syndrome?Frontiers in immunology · 2013
    Review
  12. Inborn errors of human IL-17 immunity underlie chronic mucocutaneous candidiasis.Current opinion in allergy and clinical immunology · 2012
    Review
  13. Article
  14. Immunity to fungal infections.Nature reviews. Immunology · 2011
    Review
  15. Pathogenesis and treatment of oral candidosis.Journal of oral microbiology · 2011
    Article
  16. Review
  17. Epithelial cells and innate antifungal defense.Journal of dental research · 2010
    Review
  18. Article
  19. Article
  20. Rethinking T cell immunity in oropharyngeal candidiasis.The Journal of experimental medicine · 2009
    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

12 authors.

K R RyanInstitute for Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
M Hong
P D Arkwright
A R Gennery
C Costigan
M Dominguez
D Denning
V McConnell
A J Cant
M Abinun
G P Spickett
D Lilic

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with chronic mucocutaneous candidiasis (CMC) suffer persistent infections with the yeast Candida. CMC includes patients with autoimmune regulator (AIRE) gene mutations who have autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED), and patients without known mutations. CMC patients have dysregulated cytokine production, and dendritic cells (DCs), as central orchestrators, may underlie pathogenic disease mechanisms. In 29 patients with CMC (13 with APECED) and controls, we generated monocyte-derived DCs, stimulated them with Candida albicans, Toll-like receptor-2/6 ligand and lipopolysaccharide to assess cytokine production [interleukin (IL)-12p70, IL-23, interferon (IFN)-gamma, IL-2, tumour necrosis factor (TNF)-alpha, IL-6, transforming growth factor-beta, IL-10, IL-5, IL-13] and cell-surface maturation marker expression (CD83, CD86, human leucocyte antigen D-related). In both APECED and non-APECED CMC patients, we demonstrate impairment of DC function as evidenced by altered cytokine expression profiles and DC maturation/activation: (1) both groups over-produce IL-2, IFN-gamma, TNF-alpha and IL-13 and demonstrate impaired DC maturation. (2) Only non-APECED patients showed markedly decreased Candida-stimulated production of IL-23 and markedly increased production of IL-6, suggesting impairment of the IL-6/IL-23/T helper type 17 axis. (3) In contrast, only APECED patients showed DC hyperactivation, which may underlie altered T cell responsiveness, autoimmunity and impaired response to Candida. We demonstrate different pathogenic mechanisms on the same immune response pathway underlying increased susceptibility to Candida infection in these patients.

Indexed as

AdolescentAdultCandidiasis, Chronic MucocutaneousCell DifferentiationCells, CulturedChildChild, PreschoolCytokinesDendritic CellsDisease SusceptibilityFemaleHumansInflammation MediatorsInterleukin-23MaleMiddle AgedCytokinesInflammation MediatorsInterleukin-23

Identifiers

PMID19037923
PMCPMC2633234

What OpenQuestion holds

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Registered trials

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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.