Cited by 1,056Immunodeficiency and Autoimmune DisordersAntifungal resistance and susceptibilityPsoriasis: Treatment and Pathogenesis

Chronic Mucocutaneous Candidiasis in Humans with Inborn Errors of Interleukin-17 Immunity

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Puel, Anne, Cypowyj, Sophie, Bustamante, Jacinta, Wright, Jill F., Liu, Luyan, Lim, Hye Kyung, Migaud, Mélanie, Israel, Laura +16 more·2011·Science

Abstract

Chronic yeast infections in the absence of other infections result from genetic deficiencies in proinflammatory host responses.

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Registry

Crossref · 10.1126/science.1200439

Cites

30 of 30 references verified0 citation errors · 0 not checkable

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  • IL-17-mediated immunity is central to mucocutaneous host defense against fungi such as C. albicans and Malassezia.

    “IL-17-mediated immunity is central to mucocutaneous host defense against fungi such as C. albicans and Malassezia [10,99,100].”

    From Host–Candida auris interactions in the skin (2026) · cites this paper as [99]

    The Abstract states that human IL-17A and IL-17F are essential for mucocutaneous immunity against C. albicans. A search for Malassezia found no passage addressing that fungus, so the source supports only the C. albicans part of the claim. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Th17 cells in different tissue sites can show distinct transcriptional profiles associated with homeostatic or pathogenic functions.

    “analysis of Th17 cells in different tissue sites has revealed that Th17 cells may exhibit distinct transcriptional profiles associated with either homeostatic or pathogenic functions”

    From TH17 cell heterogeneity and its role in tissue inflammation (2023) · cites this paper as [43]

  • SFB-specific intestinal homeostatic Th17 cells have a transcriptome that differs markedly from pro-inflammatory Th17 cells elicited by H. hepaticus in mice defective for induced intestinal Treg cells.

    “intestinal non-pathogenic/homeostatic Th17 cells specific for segmented filamentous bacteria (SFB) have a transcriptome that differs markedly from the pro-inflammatory Th17 cells elicited by Helicobacter hepaticus (H. hepaticus) in mice defective for induced intestinal Treg cells”

    From TH17 cell heterogeneity and its role in tissue inflammation (2023) · cites this paper as [43]

  • In the Il10−/− model of colitis, Th17 cells are the main immune population mediating the inflammatory response.

    “In the Il10−/− model of colitis, in which IL-10-deficient mice develop spontaneous microbiota-dependent colitis, Th17 cells were identified as the main immune population mediating the inflammatory immune response [43, 133].”

    From TH17 cell heterogeneity and its role in tissue inflammation (2023) · cites this paper as [43]

  • In Helicobacter hepaticus-dependent colitis, pathobiont-specific inflammatory Th17 cells are major mediators of intestinal inflammation.

    “In Helicobacter hepaticus- dependent colitis, pathobiont-specific inflammatory Th17 cells are major mediators of intestinal inflammation [43].”

    From TH17 cell heterogeneity and its role in tissue inflammation (2023) · cites this paper as [43]

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Cites

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Research works printed but not linked: 29

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  7. [8]Puel A J Exp Med 207 291 2 15 2010 20123958 PMC2822614
  8. [9]Williamson DM Br J Dermatol 81 125 2 1969 5767066
  9. [10]Leroy D Dompmartin A Houtteville JP Theron J Dermatologica 178 43 1989 2492956
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Authors
Puel, A., Cypowyj, S., Bustamante, J., Wright, J. F., Liu, L., Lim, H. K., Migaud, M., Israel, L., Chrabieh, M., Audry, M., Gumbleton, M., Toulon, A., Bodemer, C., El-Baghdadi, J., Whitters, M., Paradis, T., Brooks, J., Collins, M., Wolfman, N. M., Al-Muhsen, S., Galicchio, M., Abel, L., Picard, C., & Casanova, J.-L.
Affiliations
  • Inserm (FR)
  • Rockefeller University (US)
  • Pfizer (United States) (US)
  • Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Institut National de la Santé et de la Recherche Médicale, U980, and University Paris Descartes, Necker Medical School, 75015 Paris, France.
  • SUNY Upstate Medical University (US)
  • Hôpital Necker-Enfants Malades (FR)
  • Unit of Genetics, Military Hospital of Instruction Mohamed V, Rabat 10000, Morocco.
  • Prince Naif Center for Immunology Research, Department of Pediatrics, College of Medicine, King Saud University, Riyadh 11461, Saudi Arabia.
  • Victor J. Vilela Children’s Hospital, Rosario, Santa Fe 2000, Argentina.
Corresponding author
  • Puel, Anne
  • Cypowyj, Sophie
  • Abel, Laurent
  • Casanova, Jean-Laurent
Venue
Science
Published
2011-04
Volume
332
Issue
6025
Pages
65-68
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2034453891
Cited by
1,056
References
30
Citations by year
2026: 26 · 2025: 35 · 2024: 29 · 2023: 54 · 2022: 52 · 2021: 64 · 2020: 76 · 2019: 57 · 2018: 67 · 2017: 84 · 2016: 81 · 2015: 76 · 2014: 94 · 2013: 95 · 2012: 103
FWCI
49.58
Type
journal article
Language
en
Open access
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Center for Research Resources (UL1RR024143)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
  • Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
Keywords
chronic mucocutaneous candidiasis, IL-17A, Candida albicans, primary immunodeficiency, autosomal recessive inheritance, autosomal dominant inheritance
MeSH terms
Candida albicans, Candidiasis, Chronic Mucocutaneous, Child, Child, Preschool, Female, Genes, Dominant, Genes, Recessive, Humans, Male, Molecular Sequence Data, Mutation, Pedigree, Signal Transduction, Interleukin-17, Receptors, Interleukin-17, Th17 Cells

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