Abstract
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare disorder caused by mutations in the autoimmune regulator (AIRE) gene, leading to defects in T cell selection. The disease manifestations include both autoimmune tissue destruction and immunodeficiency, with specific susceptibility to chronic mucocutaneous candidiasis. Studies have demonstrated a wide repertoire of high affinity tissue-and cytokine-specific antibodies in patients with APECED. Here, we review the antigenic targets and function of these disease-causing and disease-ameliorating antibodies.
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Kashem, S. W., & Binstadt, B. A. (2017, March 1). Pathogenic and protective autoantibodies in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). Antibodies. MDPI. https://doi.org/10.3390/antib6010001
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