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Updated: Sep 30, 2025

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
The Immunogenetics of Autoimmune Blistering Diseases
Diana Kneiber1, Eric H Kowalski1, Kyle T Amber2,3
1Department of Dermatology, University of Illinois at Chicago, Chicago, USA.
Abstract:
Dermatological conditions constituting the group of autoimmune blistering diseases (AIBD) are characterized by loss of immunotolerance and humoral, as well as cellular, autoimmune responses that result in the development of bullae and erosions on the skin and mucous membranes. AIBDs are broadly categorized into pemphigus and pemphigoid classes with several distinct subtypes amongst them. Advances in genetics have allowed for the study and identification of alleles, and even single nucleotide polymorphisms, that harbor increased susceptibility or confer protection for the development of these conditions. The focus of this chapter pertains to a comprehensive review of the known genetic associations with AIBDs, including HLA class I-III, as well as non-HLA genes and non-coding sequences that influence cellular processes and signaling pathways.
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