Evidence map›Paper›PMID 25547797›Full record

ArticleInfection and immunity2015

CX3CR1 is dispensable for control of mucosal Candida albicans infections in mice and humans.

Timothy J Break, Martin Jaeger, Norma V Solis, Scott G Filler, Carlos A Rodriguez, Jean K Lim, Chyi-Chia Richard Lee, Jack D Sobel, Mihai G Netea, Michail S Lionakis

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

28 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. A New Phenotype inmBio · 2023
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  6. Review
  7. Review
  8. Review
  9. Article
  10. Polymorphisms within theInfection and immunity · 2020
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  11. Review
  12. Improved in vitro and in vivo Anti-International journal of nanomedicine · 2020
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  13. Article
  14. Article
  15. Genome Sequence for Candida albicans Clinical Oral Isolate 529L.Microbiology resource announcements · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. CX3CR1Science (New York, N.Y.) · 2018
    Article
  20. 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

10 authors at 7 institutions in 2 countries.

Timothy J BreakFungal Pathogenesis Unit, Laboratory of Clinical Infectious Disease, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.
Martin JaegerRadboud University Medical Center and Radboud Center for Infectious Diseases (RCI), Nijmegen, The Netherlands.
Norma V SolisDivision of Infectious Diseases, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, USA.
Scott G FillerDivision of Infectious Diseases, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, USA The David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Carlos A RodriguezDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Jean K LimDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Chyi-Chia Richard LeeLaboratory of Pathology, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Jack D SobelDepartment of Infectious Diseases, Wayne State University School of Medicine, Detroit, Michigan, USA.
Mihai G NeteaRadboud University Medical Center and Radboud Center for Infectious Diseases (RCI), Nijmegen, The Netherlands.
Michail S LionakisFungal Pathogenesis Unit, Laboratory of Clinical Infectious Disease, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA lionakism@niaid.nih.gov.
Harbor–UCLA Medical Center · USIcahn School of Medicine at Mount Sinai · USNational Institute of Allergy and Infectious Diseases · USNational Cancer Institute · USRadboud University Medical Center · NLRadboud University Nijmegen · NLWayne State University · US

Funding

Immunopathogenesis of Fungal InfectionsZIAAI001175 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LIONAKIS, MICHAIL · 2012 to 2025
$23.9M
Candida albicans Epithelial Cell Interactions and Oropharyngeal DiseaseR01DE017088 · NIDCR · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI FILLER, SCOTT G · 2005 to 2014
$3.4M
European Research Council 310372Intramural NIH HHSNIDCR NIH HHS R01 DE017088NIDCR NIH HHS R01DE017088
6 · The paper itself

Abstract

Candida albicans is part of the normal commensal microbiota of mucosal surfaces in a large percentage of the human population. However, perturbations of the host's immune response or bacterial microbiota have been shown to predispose individuals to the development of opportunistic Candida infections. It was recently discovered that a defect in the chemokine receptor CX3CR1 increases susceptibility of mice and humans to systemic candidiasis. However, whether CX3CR1 confers protection against mucosal C. albicans infection has not been investigated. Using two different mouse models, we found that Cx3cr1 is dispensable for the induction of interleukin 17A (IL-17A), IL-22, and IL-23 in the tongue after infection, as well as for the clearance of mucosal candidiasis from the tongue or lower gastrointestinal (GI) tract colonization. Furthermore, the dysfunctional human CX3CR1 allele CX3CR1-M280 was not associated with development of recurrent vulvovaginal candidiasis (RVVC) in women. Taken together, these data indicate that CX3CR1 is not essential for protection of the host against mucosal candidiasis, underscoring the dependence on different mammalian immune factors for control of mucosal versus systemic Candida infections.

Indexed as

AllelesAnimalsCandida albicansCandidiasisCandidiasis, VulvovaginalCX3C Chemokine Receptor 1Disease Models, AnimalFemaleGastrointestinal TractGene ExpressionHost-Pathogen InteractionsHumansInterleukin-17Interleukin-22Interleukin-23InterleukinsCX3C Chemokine Receptor 1CX3CR1 protein, humanIL17A protein, humanInterleukin-17Interleukin-22Interleukin-23InterleukinsReceptors, Chemokine

Identifiers

PMID25547797
PMCPMC4333470
OpenAlexW1963593559

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.