Drug Development in Pemphigoid Diseases

Acta Derm Venereol. 2020 Feb 12;100(5):adv00055. doi: 10.2340/00015555-3400.

Abstract

Pemphigoid diseases are organ-specific autoimmune diseases of the skin and/or mucous membranes. They are caused by autoantibodies targeting adhesion molecules located at the dermal-epidermal junction. While the diagnostics of pemphigoid diseases and insights into their pathogenesis have improved significantly, the development of novel treatments that are effective and safe remains an unmet medical need. However, numerous pre-clinical studies and early clinical trials have recently been launched. This review summarizes some pathways leading to drug development in pemphigoid diseases, namely: (i) hypothesis-driven drug development; (ii) omics-based drug development; (iii) drug repurposing; (iv) screening-based drug development; and (v) drug development based on careful clinical observations. Ultimately, it is hoped that this will lead to personalized and curative treatments.

Keywords: animal autoantibodies; disease models; epidermolysis bullosa acquisita; translational medical research; bullous pemphigoid.

Publication types

  • Review

MeSH terms

  • Autoantibodies / drug effects
  • Autoimmune Diseases / drug therapy*
  • Autoimmune Diseases / pathology
  • Cell Adhesion Molecules / immunology
  • Dimethyl Fumarate / therapeutic use
  • Doxycycline / therapeutic use
  • Drug Development*
  • Epidermolysis Bullosa Acquisita / drug therapy
  • Epidermolysis Bullosa Acquisita / immunology
  • Epidermolysis Bullosa Acquisita / pathology
  • Female
  • Forecasting
  • Humans
  • Male
  • Molecular Targeted Therapy / methods
  • Pemphigoid, Bullous / drug therapy*
  • Pemphigoid, Bullous / immunology*
  • Pemphigoid, Bullous / pathology
  • Protein-Tyrosine Kinases / administration & dosage*
  • Skin Diseases, Vesiculobullous / drug therapy
  • Skin Diseases, Vesiculobullous / immunology
  • Skin Diseases, Vesiculobullous / pathology
  • Translational Research, Biomedical

Substances

  • Autoantibodies
  • Cell Adhesion Molecules
  • Protein-Tyrosine Kinases
  • Dimethyl Fumarate
  • Doxycycline