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Activity of apremilast in a patient with severe pemphigus vulgaris: case report.
Delvaux, Cheyenne; Bohelay, Gérôme; Sitbon, Ishaï-Yaacov; Soued, Isaac; Alexandre, Marina; Cucherousset, Joël; Gilardin, Laurent; Diep, Antoine; Caux, Frédéric; Le Roux-Villet, Christelle.
Afiliação
  • Delvaux C; Department of Dermatology, Saint-Pierre and Brugmann University Hospitals, Université Libre de Bruxelles, Brussels, Belgium.
  • Bohelay G; Department of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
  • Sitbon IY; Department of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
  • Soued I; Department of ENT, Avicenne Hospital AP-HP, Sorbonne Paris Nord University, Bobigny, France.
  • Alexandre M; Department of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
  • Cucherousset J; Department of Pathology, Avicenne Hospital AP-HP, Sorbonne Paris Nord University, Bobigny, France.
  • Gilardin L; Department of Internal Medicine, Jean-Verdier Hospital, Bondy, France.
  • Diep A; Department of Immunology, Saint-Louis Hospital, Paris, France.
  • Caux F; Department of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
  • Le Roux-Villet C; Department of Dermatology and Referral Center for Autoimmune Bullous Diseases MALIBUL, Avicenne Hospital, AP-HP, Sorbonne Paris Nord University, Bobigny, France.
Front Immunol ; 15: 1404185, 2024.
Article em En | MEDLINE | ID: mdl-38983857
ABSTRACT

Introduction:

Although the treatment for pemphigus vulgaris (PV) has been revolutionized by the use of rituximab combined with corticosteroids, new effective therapies with a better safety profile are needed. Observation A 67-year-old woman was diagnosed with severe mucosal PV, which was initially misdiagnosed as atypical Behçet's disease. Following an unsuccessful colchicine treatment, significant improvement was observed upon the introduction of apremilast reduced pain, fewer lesions, and a stabilized weight. The discontinuation of apremilast led to a rapid relapse. Retrospective analysis through anti-Dsg3 ELISA indicated a gradual decrease in antibody levels during the apremilast treatment.

Discussion:

Apremilast, a phosphodiesterase 4 inhibitor approved for psoriasis and Behçet's disease's related oral ulcers treatment, demonstrated its efficacy in this PV case. This is the second case report highlighting the effectiveness of apremilast for PV treatment. Apremilast's ability to upregulate cyclic adenosine monophosphate (cAMP) levels appears to contribute to the stabilization of keratinocyte adhesion.

Conclusion:

Apremilast may be a promising therapeutic option for the treatment of pemphigus, with an innovative mechanism of action, no induced immunosuppression, and good tolerance. It could be a good alternative to steroids, in the treatment regimen of steroids combined with rituximab.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Talidomida / Pênfigo Limite: Aged / Female / Humans Idioma: En Revista: Front Immunol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Talidomida / Pênfigo Limite: Aged / Female / Humans Idioma: En Revista: Front Immunol Ano de publicação: 2024 Tipo de documento: Article