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DOI 10.1016/s0923-1811(03)00035-5

Медицинская библиотека · Journal of dermatological science · 2003

Cicatricial pemphigoid sera specifically react with the most C-terminal portion of BP180.

Lee Jee Bum, Liu Yuanlin, Hashimoto Takashi

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

cicatricial pemphigoid and bullous pemphigoid are characterized by circulating autoantibodies to the hemidesmosomal protein, BP180. Different clinical features between cicatricial pemphigoid and bullous pemphigoid appear to correlate with distinct target epitopes on BP180. Previous studies demonstrated that the majority of bullous pemphigoid sera react with immunodominant membrane-proximal non-collagenous domain (NC16a) on the extracellular portion of BP180, whereas cicatricial pemphigoid antibodies are directed to the C-terminal domains of BP180. However, the fine sites within the C-terminal domain of BP180 recognized by autoantibodies in patients with cicatricial pemphigoid and bullous pemphigoid have not yet been clearly elucidated.

OBJECTIVES

the aim of the present study was to analyze the fine specificity of the reactivity within the C-terminal domain of BP180 for the autoantibodies in sera from patients with cicatricial pemphigoid, and to compare the reactivity with that of bullous pemphigoid sera.

METHODS AND

RESULTS

we generated three recombinant proteins with 101 amino acids, which together cover the C-terminal domain of BP180. We confirmed that cicatricial pemphigoid sera mainly react with most C-terminal portion, whereas bullous pemphigoid sera react with more N-terminal domains.

CONCLUSION

this study implicated that autoantibodies of sera from patients with cicatricial pemphigoid and bullous pemphigoid reacted differently within C-terminal domain of BP180.

Для цитирования: Lee Jee Bum, Liu Yuanlin, Hashimoto Takashi. Cicatricial pemphigoid sera specifically react with the most C-terminal portion of BP180.. Journal of dermatological science. 2003. DOI: 10.1016/s0923-1811(03)00035-5.

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