Abstract

Introduction: The in situ immune response within skin biopsies from patients affected by autoimmune skin blistering diseases (ABDs) is not well characterized. Aim: Based on the fact that the ABD immune response is considered an adaptive immune response, both an innate immune response and inflammation would be expected in these diseases. Our investigation investigates the presence of cyclo-oxygenase-2 (COX-2), since this enzyme is commonly involved in innate immune responses. Methods: We utilized immunohistochemistry (IHC) to evaluate the presence of COX-2 in lesional skin biopsies of patients affected by ABDs. We tested 30 patients with endemic pemphigus foliaceus (EPF), 15 controls from the endemic area, and 15 biopsies from healthy controls from the USA. We also tested archival biopsies from patients with selected ABDs, including 20 patients with bullous pemphigoid, 20 with pemphigus vulgaris, 8 with pemphigus foliaceus and 12 with dermatitis herpetiformis. Results: Most ABD biopsies stained positive for COX-2 in the lesional blister and/or the dermal inflammatory infiltrate, accentuated in the upper neurovascular plexus. In BP and EPF, the COX-2 staining was also seen in the sweat glands. All controls were negative. Conclusions: We document that COX-2 is expressed in lesional skin of patients with ABDs.

Highlights

  • The in situ immune response within skin biopsies from patients affected by autoimmune skin blistering diseases (ABDs) is not well characterized

  • Because adaptive immunity has been demonstrated to be play a pathogenic role in autoimmune blistering skin diseases (ABDs), it is important to note that innate immunity is the first step in an adaptive immune response

  • Few studies have studied molecules involved in the adaptive immune response in ABDs

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Summary

Introduction

The in situ immune response within skin biopsies from patients affected by autoimmune skin blistering diseases (ABDs) is not well characterized. Methods: We utilized immunohistochemistry (IHC) to evaluate the presence of COX-2 in lesional skin biopsies of patients affected by ABDs. We tested 30 patients with endemic pemphigus foliaceus (EPF), 15 controls from the endemic area, and 15 biopsies from healthy controls from the USA. Conclusions: We document that COX-2 is expressed in lesional skin of patients with ABDs. Multiple therapies have been utilized for the treatment of cutaneous autoimmune blistering skin diseases (ABDs). The present investigation aims to study an inducible marker of the innate immune response, the presence of cyclo-oxygenase 2 (COX-2); this enzyme generates inflammatory prostanoids, and inflammation is a hallmark of multiple ABDs. we studied the in situ immune response by performing immunohistochemistry (IHC) stains on lesional skin biopsies for COX-2.

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