Autoimmunity to deltaNp63alpha in chronic ulcerative stomatitis

被引:20
作者
Solomon, L. W.
Neiders, M. E.
Zwick, M. G.
Kirkwood, K. L.
Kumar, V.
机构
[1] Tufts Univ, Sch Dent Med, Dept Oral & Maxillofacial Pathol, Boston, MA 02111 USA
[2] SUNY Buffalo, Sch Dent Med, Dept Oral Diagnost Sci, Buffalo, NY 14260 USA
[3] IMMCO Diagnost Inc, Buffalo, NY USA
[4] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
[5] SUNY Buffalo, Dept Microbiol, Buffalo, NY 14260 USA
[6] SUNY Buffalo, Dept Dermatol, Buffalo, NY 14260 USA
关键词
p63; chronic ulcerative stomatitis; autoimmunity; ORAL MUCOSAL DISEASE; TOPICAL CORTICOSTEROIDS; LIVING CELLS; P53; HOMOLOG; P63; P73; AUTOANTIBODIES; EXPRESSION; ANTIBODIES; PROTEIN;
D O I
10.1177/154405910708600904
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Chronic ulcerative stomatitis ( CUS) is a recently described mucocutaneous condition in which patients experience chronic, painful, ulcerative lesions of the oral mucosa. CUS is diagnosed by immunofluorescence studies that demonstrate antinuclear antibodies. These autoantibodies are specific for a protein, deltaNp63alpha, which is normally expressed in basal cell nuclei of stratified squamous epithelia. The purpose of this study was to characterize the autoimmune response in CUS. Protein antigens were produced by in vitro transcription/ translation of polymerase chain-reaction ( PCR)- amplified cDNAs. We used immunoblotting and immunoprecipitation experiments with serum from CUS patients to examine the ( 1) antibody isotype, ( 2) immunogenic functional domains of the deltaNp63alpha antigen, and ( 3) cross-reactivity with homologous p53, p73, and p63 proteins. Results demonstrate CUS patient antibodies to deltaNp63alpha, and 52% of cases have circulating IgA isotype antibodies. The N-terminal and DNA-binding domains are the immuno dominant regions, and antibody cross-reactivity with p53, p63, and p73 isoforms is limited.
引用
收藏
页码:826 / 831
页数:6
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