Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2004 Mar;135(3):348-57.
doi: 10.1111/j.1365-2249.2004.02384.x.

Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED): a model disease to study molecular aspects of endocrine autoimmunity

Affiliations
Review

Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED): a model disease to study molecular aspects of endocrine autoimmunity

P Peterson et al. Clin Exp Immunol. 2004 Mar.
No abstract available

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Schematic of the AIRE protein showing the functional protein domains, and the distribution of the APECED-causing mutations for which functional and/or localization data is available (see also Table 3). HSR: homogenously staining region; SAND: Sp100, AIRE, NucP41/75 and DEAF-1; PHD: plant homeodomain zinc finger; PRR, proline rich region; L, LXXLL nuclear receptor interaction motif.
Fig. 2
Fig. 2
Subcellular localization of the AIRE protein, as illustrated by immunofluorescence staining of AIRE-expressing cells with a monoclonal anti-AIRE antibody. Three typical staining patterns are demonstrated. (a) in this cell AIRE is seen both in the cytoplasm and nucleus. (b) AIRE is seen only in the nucleus, as a diffuse staining, and in nuclear dots. (c) AIRE is seen only in the cytoplasm in typical filaments.
Fig. 3
Fig. 3
AIRE expression is controlled by the lymphotoxin pathway. The classical (a) and alternative (b) paths of activation through the lymphotoxin beta receptor are shown. LTα and LTβ: lymphotoxin alpha and beta, respectively; LTβR, lymphotoxin beta receptor; IKK alpha and beta, I kappa B kinase alpha and beta, respectively. Adapted from Derudder et al., Muller et al. and Mordmuller et al. [–94].
Fig. 4
Fig. 4
AIRE and negative selection in the thymus. One of the APECED autoantigens, P450c21, is used as an example. Under normal circumstances (upper portion), AIRE drives the expression of autoantigens in thymic medullary epithelial cells (MECs), resulting finally in the negative selection of T cells reactive to these autoantigens. In APECED, with dysfunctional AIRE, the autoreactive T cells escape selection with the inevitable consequence of autoimmune attack against the target organs expressing the autoantigens.

References

    1. Neufeld M, Maclaren NK, Blizzard RM. Two types of autoimmune Addison's disease associated with differen polyglandular autoimmune (PGA) syndromes. Medicine (Baltimore) 1981;60:355–62. - PubMed
    1. Blizzard RM, Kyle M. Studies of the adrenal antigens and antibodies in Addison's disease. J Clin Invest. 1963;42:1653–60. - PMC - PubMed
    1. Ahonen P, Myllärniemi S, Sipila I, et al. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. N Engl J Med. 1990;322:1829–36. - PubMed
    1. Perheentupa JAPS-I APECED. the clinical disease and therapy. Endocrinol Metabol Clin N Am. 2002;31:295–320. - PubMed
    1. Björses P, Aaltonen J, Vikman A, et al. Genetic homogeneity of autoimmune polyglandular disease type I. Am J Human Genet. 1996;59:879–86. - PMC - PubMed

Publication types

MeSH terms