Autoantibodies to early endosome antigen (EEA1) produce a staining pattern resembling cytoplasmic anti-neutrophil cytoplasmic antibodies (C-ANCA)
S. Selak
Faculty of Medicine, University of Calgary, Calgary, Canada
Search for more papers by this authorR. C. Woodman
Faculty of Medicine, University of Calgary, Calgary, Canada
Search for more papers by this authorM. J. Fritzler
Faculty of Medicine, University of Calgary, Calgary, Canada
Search for more papers by this authorS. Selak
Faculty of Medicine, University of Calgary, Calgary, Canada
Search for more papers by this authorR. C. Woodman
Faculty of Medicine, University of Calgary, Calgary, Canada
Search for more papers by this authorM. J. Fritzler
Faculty of Medicine, University of Calgary, Calgary, Canada
Search for more papers by this authorAbstract
Autoantibodies to EEA1 have been described in patients with neurological diseases, subacute cutaneous lupus and a variety of other conditions, including a patient with Wegener's granulomatosis (WG). EEA1 is a hydrophilic peripheral membrane protein transiently associated with the cytoplasmic face of early endosomes. Antibodies to EEA1 produce a staining pattern that resembles the C-ANCA pattern produced by anti-proteinase 3 (PR3) antibodies in WG sera. Co-localization studies show incomplete overlap of the staining produced by anti-EEA1 with anti-PR3. We showed that 0/40 unselected sera, from a cohort of WG patients and antibodies to PR3, reacted with EEA1. In addition, 1/15 sera that have a C-ANCA staining pattern but do not react with PR3 in an ELISA, immunoprecipitated the recombinant EEA1 protein. We conclude that although antibodies to EEA1 produce a staining pattern that resembles anti-PR3 and C-ANCA, antibodies to EEA1 in WG are rare. However, some C-ANCA+ sera that do not react with PR3 may contain EEA1 autoantibodies.
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