Persistence of IgG4 as a potential serological marker of disease activity in patients with epidermolysis bullosa acquisita treated with rituximab

Author:

Gordilho J. O.1ORCID,Miyamoto D.1,Maruta C. W.1,Santo R. M.2,Mahmoud A.3,Navarro‐Rodriguez T.4,Werneck‐Silva A. L.4,de Aguiar L. M.5,Borges I. C.6,Santi C. G.1,Aoki V.1ORCID

Affiliation:

1. Department of Dermatology, Faculdade de Medicina FMUSP Universidade de São Paulo Sao Paulo, SP Brazil

2. Department of Ophthalmology, Faculdade de Medicina FMUSP Universidade de São Paulo Sao Paulo, SP Brazil

3. Department of Otorhinolaryngology, Faculdade de Medicina FMUSP Universidade de São Paulo Sao Paulo, SP Brazil

4. Department of Gastroenterology, Faculdade de Medicina FMUSP Universidade de São Paulo Sao Paulo, SP Brazil

5. Department of Ginecology, Faculdade de Medicina FMUSP Universidade de São Paulo Sao Paulo, SP Brazil

6. Department of Infectious Diseases, Faculdade de Medicina FMUSP Universidade de São Paulo Sao Paulo, SP Brazil

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Reference10 articles.

1. Epidermolysis bullosa acquisita: A comprehensive review

2. Epidermolysis bullosa acquisita

3. Pathogenicity of IgG subclass autoantibodies to type VII collagen: Induction of dermal–epidermal separation

4. The use of rituximab in treatment of epidermolysis bullosa acquisita: Three new cases and a review of the literature

5. A case report of the use of rituximab and the epidermolysis bullosa disease activity scoring index (EBDASI) in a patient with epidermolysis bullosa Acquisita with extensive esophageal involvement;Yang A;Acta Dermatovenerol Croat,2018

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