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Effect of Anti-CD20 Monoclonal Antibody (Rituximab) on Recalcitrant Pemphigus Vulgaris / 대한피부과학회지
Article in Ko | WPRIM | ID: wpr-204122
Responsible library: WPRO
ABSTRACT

BACKGROUND:

Pemphigus is a severe blistering disorder caused by autoantibodies to desmogleins 1 and 3. Because some patients with pemphigus never enter into remission, new immunosuppressants are warranted. Rituximab is a chimeric monoclonal antibody binding to the CD20 antigen on B cells, which proved to be effective in recalcitrant pemphigus.

OBJECTIVE:

The purpose of this study was to evaluate the efficacy and safety of Rituximab in the treatment of refractory pemphigus vulgaris.

METHODS:

A retrospective analysis was conducted of six patients with recalcitrant pemphigus vulgaris in Yongdong Severance Hospital. Rituximab was administered intravenously at a dosage of 375 mg/m(2) body surface area. Five patient received 2 cycles of Rituximab treatment with an interval of 7 days. One patient received 5 cycles of treatment. The mean follow-up after treatment was 9.3 months (range, 2 months to 16 months).

RESULTS:

All the patients presented clinical improvements. The average pemphigus vulgaris severity score decreased from 12.2 to 2.5 after treatment. No adverse effects were observed.

CONCLUSION:

Rituximab has been proved as an effective and safe treatment for refractory pemphigus vulgaris.
Subject(s)
Key words
Full text: 1 Index: WPRIM Main subject: Autoantibodies / Body Surface Area / B-Lymphocytes / Retrospective Studies / Follow-Up Studies / Blister / Pemphigus / Antigens, CD20 / Desmogleins / Antibodies, Monoclonal, Murine-Derived Type of study: Observational_studies / Prognostic_studies Limits: Humans Language: Ko Journal: Korean Journal of Dermatology Year: 2008 Type: Article
Full text: 1 Index: WPRIM Main subject: Autoantibodies / Body Surface Area / B-Lymphocytes / Retrospective Studies / Follow-Up Studies / Blister / Pemphigus / Antigens, CD20 / Desmogleins / Antibodies, Monoclonal, Murine-Derived Type of study: Observational_studies / Prognostic_studies Limits: Humans Language: Ko Journal: Korean Journal of Dermatology Year: 2008 Type: Article