| Literature DB >> 26084804 |
Nils Landegren1, Donald Sharon2, Anthony K Shum3, Imran S Khan4, Kayla J Fasano4, Åsa Hallgren5, Caroline Kampf6, Eva Freyhult7, Brita Ardesjö-Lundgren8, Mohammad Alimohammadi9, Sandra Rathsman10, Jonas F Ludvigsson11, Dan Lundh12, Ruben Motrich13, Virginia Rivero13, Lawrence Fong14, Aleksander Giwercman15, Jan Gustafsson16, Jaakko Perheentupa17, Eystein S Husebye18, Mark S Anderson4, Michael Snyder19, Olle Kämpe5.
Abstract
Autoimmune polyendocrine syndrome type 1 (APS1), a monogenic disorder caused by AIRE gene mutations, features multiple autoimmune disease components. Infertility is common in both males and females with APS1. Although female infertility can be explained by autoimmune ovarian failure, the mechanisms underlying male infertility have remained poorly understood. We performed a proteome-wide autoantibody screen in APS1 patient sera to assess the autoimmune response against the male reproductive organs. By screening human protein arrays with male and female patient sera and by selecting for gender-imbalanced autoantibody signals, we identified transglutaminase 4 (TGM4) as a male-specific autoantigen. Notably, TGM4 is a prostatic secretory molecule with critical role in male reproduction. TGM4 autoantibodies were detected in most of the adult male APS1 patients but were absent in all the young males. Consecutive serum samples further revealed that TGM4 autoantibodies first presented during pubertal age and subsequent to prostate maturation. We assessed the animal model for APS1, the Aire-deficient mouse, and found spontaneous development of TGM4 autoantibodies specifically in males. Aire-deficient mice failed to present TGM4 in the thymus, consistent with a defect in central tolerance for TGM4. In the mouse, we further link TGM4 immunity with a destructive prostatitis and compromised secretion of TGM4. Collectively, our findings in APS1 patients and Aire-deficient mice reveal prostate autoimmunity as a major manifestation of APS1 with potential role in male subfertility.Entities:
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Year: 2015 PMID: 26084804 DOI: 10.1126/scitranslmed.aaa9186
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956