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Front Immunol. 2017 Sep 01;8:1074. doi: 10.3389/fimmu.2017.01074. eCollection 2017.

Altered Immune Activation and IL-23 Signaling in Response to .

Frontiers in immunology

Øyvind Bruserud, Eirik Bratland, Alexander Hellesen, Nicolas Delaleu, Håkon Reikvam, Bergithe E Oftedal, Anette S B Wolff

Affiliations

  1. Department of Clinical Science, University of Bergen, Bergen, Norway.
  2. Broegelmann Research Laboratory, Department of Clinical Science, University of Bergen, Bergen, Norway.
  3. Swiss Institute of Bioinformatics, Lausanne, Switzerland.
  4. Computational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway.
  5. Department of Medicine, Haukeland University Hospital, Bergen, Norway.

PMID: 28919897 PMCID: PMC5585148 DOI: 10.3389/fimmu.2017.01074

Abstract

OBJECTIVE: Autoimmune polyendocrine syndrome type 1 (APS-1) is a rare, childhood onset disease caused by mutations in the

METHODS: Whole blood was stimulated with

RESULTS: We found an altered immune response in APS-1 patients compared with healthy controls. Patients fail to increase the essential ILs, such as IL-2, IL-17A, IL-22, and IL-23, when stimulating whole blood with

CONCLUSION: APS-1 patients have an altered immune response to

Keywords: IL-17; IL-22; IL-23; autoimmune polyendocrine syndrome type 1; chronic mucocutaneous candidiasis; monocytes

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