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Arch Dermatol Res ; 308(1): 31-8, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26498290

RESUMO

Bullous pemphigoid (BP) is an autoimmune blistering skin disease associated with autoantibodies against two hemidesmosomal proteins, BP180 (type XVII collagen) and BP230. As the pathogenic relevance of antibodies against the immunodominant NC16A domain of BP180 has been clearly demonstrated, specific removal of these antibodies should be a rational therapeutic approach. Here, we evaluated three recombinant forms of bacterially produced BP180 NC16A, a monomer, trimer, and tetramer, together with different matrices for their efficacy to specifically adsorb autoantibodies from BP plasma samples. An adsorber consisting of NC16A-trimer coupled to NHS-activated Sepharose 4 Fast Flow revealed satisfying adsorption rates and a high specificity. The NC16A-trimer adsorber was regenerable and autoclavable. It has the potential to be used for specific immunoadsorption to treat severe and refractory BP and other pemphigoid diseases associated with BP180 NC16A reactivity.


Assuntos
Autoanticorpos/sangue , Remoção de Componentes Sanguíneos/instrumentação , Remoção de Componentes Sanguíneos/métodos , Penfigoide Bolhoso/sangue , Penfigoide Bolhoso/terapia , Adolescente , Idoso , Idoso de 80 Anos ou mais , Autoanticorpos/imunologia , Autoantígenos/imunologia , Proteínas de Transporte/imunologia , Proteínas do Citoesqueleto/imunologia , Distonina , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Proteínas do Tecido Nervoso/imunologia , Colágenos não Fibrilares/imunologia , Penfigoide Bolhoso/imunologia , Estrutura Terciária de Proteína , Sefarose/metabolismo , Colágeno Tipo XVII
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