Evidence map›Paper›PMID 24186907›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2014

Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency.

Monia Ouederni, Ozden Sanal, Aydan Ikinciogullari, Ilhan Tezcan, Figen Dogu, Ithaisa Sologuren, Sigifredo Pedraza-Sánchez, Melike Keser, Gonul Tanir, Chris Nieuwhof and 32 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

60 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. Interferon Gamma in Sickness Predisposing toBalkan medical journal · 2024
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  3. Article
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  5. Review
  6. The Th17/IL-17 Axis and Host Defense Against Fungal Infections.The journal of allergy and clinical immunology. In practice · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Autosomal recessiveFrontiers in immunology · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Inherited human IFN-γ deficiency underlies mycobacterial disease.The Journal of clinical investigation · 2020
    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

42 authors at 20 institutions in 18 countries.

Monia OuederniPediatric Hematology-Immunology Unit, National Bone Marrow Transplantation Center, Tunis.
Ozden Sanal
Aydan Ikinciogullari
Ilhan Tezcan
Figen Dogu
Ithaisa Sologuren
Sigifredo Pedraza-Sánchez
Melike Keser
Gonul Tanir
Chris Nieuwhof
Elena Colino
Dinakantha Kumararatne
Jacov Levy
Necil Kutukculer
Caner Aytekin
Estefanía Herrera-Ramos
Micah Bhatti
Neslihan Karaca
Ridha Barbouche
Arnon Broides
Ekaterini Goudouris
José Luis Franco
Nima Parvaneh
Ismail Reisli
Alexis Strickler
Anna Shcherbina
Ayper Somer
Anthony Segal
Alfonso Angel-Moreno
José Luis Lezana-Fernandez
Mohamed Bejaoui
Miriam Bobadilla-Del Valle
Salem Kachboura
Timothy Sentongo
Imen Ben-Mustapha
Jacinta Bustamante
Capucine Picard
Anne Puel
Stéphanie Boisson-Dupuis
Laurent Abel
Jean-Laurent Casanova
Carlos Rodríguez-Gallego
Inserm · FRAnkara University · TRBen-Gurion University of the Negev · ILEge University · TRHospital Universitario de Gran Canaria Doctor Negrín · ESInstitut Pasteur de Tunis · TNIstanbul University · TRMinistry of Health · TRUniwersytecki Szpital Dziecięcy · PLAddenbrooke's Hospital · GBComer Children's Hospital · USHôpital Necker-Enfants Malades · FRHospital Infantil de México Federico Gómez · MXHospital Universitario Insular de Gran Canaria · ESInstituto Tecnológico del Salmón · CLInstitut Supérieur des Études Technologiques en Communications de Tunis · TNIran University of Medical Sciences · IRLaboratoire de Biochimie · FRMaastricht University Medical Centre · NLNational Institute Of Blood Disease and Bone Marrow Transplantation · PK

Funding

Transforming Translational Science and Education to Benefit Human HealthUL1TR000043 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2012 to 2015
$26.8M
Genome-Wide Dissection of Mendelian Susceptibility to Mycobacterial DiseaseR37AI095983 · NIAID · ROCKEFELLER UNIVERSITY · PI CASANOVA, JEAN-LAURENT · 2011 to 2020
$4.6M
A genetic dissection of Mendelian susceptibility to mycobacterial diseases (MSMD)R01AI089970 · NIAID · ROCKEFELLER UNIVERSITY · PI CASANOVA, JEAN-LAURENT · 2010 to 2014
$2.5M
NCATS NIH HHS UL1 TR000043NIAID NIH HHS R01 AI089970NIAID NIH HHS R37 AI095983
6 · The paper itself

Abstract

backgroundInterleukin 12Rβ1 (IL-12Rβ1)-deficient patients are prone to clinical disease caused by mycobacteria, Salmonella, and other intramacrophagic pathogens, probably because of impaired interleukin 12-dependent interferon γ production. About 25% of patients also display mucocutaneous candidiasis, probably owing to impaired interleukin 23-dependent interleukin 17 immunity. The clinical features and outcome of candidiasis in these patients have not been described before, to our knowledge. We report here the clinical signs of candidiasis in 35 patients with IL-12Rβ1 deficiency.

resultsMost (n = 71) of the 76 episodes of candidiasis were mucocutaneous. Isolated oropharyngeal candidiasis (OPC) was the most common presentation (59 episodes, 34 patients) and was recurrent or persistent in 26 patients. Esophageal candidiasis (n = 7) was associated with proven OPC in 2 episodes, and cutaneous candidiasis (n = 2) with OPC in 1 patient, whereas isolated vulvovaginal candidiasis (VVC; n = 3) was not. Five episodes of proven invasive candidiasis were documented in 4 patients; 1 of these episodes was community acquired in the absence of any other comorbid condition. The first episode of candidiasis occurred earlier in life (median age±standard deviation, 1.5 ± 7.87 years) than infections with environmental mycobacteria (4.29 ± 11.9 years), Mycobacterium tuberculosis (4 ± 3.12 years), or Salmonella species (4.58 ± 4.17 years) or other rare infections (3 ± 11.67 years). Candidiasis was the first documented infection in 19 of the 35 patients, despite the vaccination of 10 of these 19 patients with live bacille Calmette-Guérin.

conclusionsPatients who are deficient in IL-12Rβ1 may have candidiasis, usually mucocutaneous, which is frequently recurrent or persistent. Candidiasis may be the first clinical manifestation in these patients.

Indexed as

AdolescentAdultCandidiasisChildChild, PreschoolFemaleHumansInfantInterleukin-12 Receptor beta 1 SubunitMaleMiddle AgedPatient Outcome AssessmentRecurrenceInterleukin-12 Receptor beta 1 SubunitCandidaInterleukin-12 receptor β1 chainMycobacteriumprimary immunodeficiencySalmonella

Identifiers

PMID24186907
PMCPMC3871796
OpenAlexW2109839976

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.