Title of article :
Autoantibodies to villin occur frequently in IPEX, a severe immune dysregulation, syndrome caused by mutation of FOXP3
Author/Authors :
Kobayashi، نويسنده , , Ichiro and Kubota، نويسنده , , Mitsuru and Yamada، نويسنده , , Masafumi and Tanaka، نويسنده , , Hiroshi and Itoh، نويسنده , , Shuichi and Sasahara، نويسنده , , Yoji and Whitesell، نويسنده , , Luke and Ariga، نويسنده , , Tadashi، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Abstract :
Intractable diarrhea is a major symptom of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome and associated with autoantibodies against enterocytes. Although autoimmune enteropathy (AIE)-related 75 kDa antigen (AIE-75) is a prominent autoantigen involved in the enteropathy associated with IPEX syndrome, some patients with this syndrome demonstrated autoantibody recognizing a 95 kDa protein rather than AIE-75 in the small intestine. We, herewith, identified villin, an actin-binding protein, as the 95 kDa antigen. Four of five sera from patients with IPEX syndrome reacted with a fusion protein of glutathione-S-transferase and full length villin (GST–villin), whereas only three of 98 control sera weakly reacted with GST–villin. Anti-AIE-75 antibody was detected in all five IPEX sera but not in normal or control disease sera. We conclude that both AIE-75 and villin appear to be brush border autoantigens in IPEX syndrome and could be used for the diagnosis of AIE in patients with presumptive IPEX syndrome.
Keywords :
villin , AIE-75 , IPEX , Autoantibody
Journal title :
Clinical Immunology
Journal title :
Clinical Immunology