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Peer-reviewed veterinary case report

Anti-desmocollin-1 IgA autoantibodies in dogs with pemphigus foliaceus

By Jordan, Tyler J M et al.Ā·Published in Veterinary immunology and immunopathologyĀ·2024Ā·North Caroline State University, United StatesĀ·View original on PubMed →

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Original publication title: Re-evaluating the prevalence of anti-desmocollin-1 IgA autoantibodies in canine pemphigus foliaceus.

Species:
dog
Skin & coatDogs

Plain-English summary

A dog with pemphigus foliaceus, an autoimmune skin disease, was studied to see if a specific type of antibody (IgA) was present in higher amounts than previously thought. This condition causes painful skin lesions and is usually linked to another type of antibody (IgG). Researchers tried to find more of the IgA antibodies by removing most of the IgG from the dog's blood samples, but they still didn't find significant levels of IgA. This suggests that IgA may not play a major role in the disease for dogs with pemphigus foliaceus.

People also search for: dog skin problems pemphigus foliaceus Ā· autoimmune skin disease in dogs Ā· treatment for dog skin lesions

Abstract

Pemphigus foliaceus (PF) is an autoimmune skin disease of dogs characterized by intraepidermal pustules containing neutrophils and dissociated keratinocytes that develop in association with circulating and tissue-bound IgG autoantibodies. A subset of IgG autoantibodies in canine PF target desmocollin-1 (DSC1), a component of intercellular adhesion complexes within the epidermis. Passive transfer of IgG autoantibodies from canine PF sera to mice was previously shown to induce skin disease in the absence of infiltrating neutrophils. In attempts to identify a mechanism responsible for neutrophil recruitment, past studies evaluated the prevalence of IgA autoantibodies in canine PF sera where they were found in <20% of affected dogs. We re-evaluated the prevalence of anti-DSC1 IgA in canine PF due to concerns regarding the sensitivity of previously used methods. We hypothesized that anti-DSC1 IgA are present in most dogs with PF but have been under-detected due to competition with concurrent anti-DSC1 IgG for binding to their mutual antigenic target. Despite removing approximately 80% of IgG from patient sera using affinity chromatography, we did not detect an increase in anti-DSC1 IgA by performing indirect immunofluorescence on canine DSC1-transfected HEK293T cells. Taken together, our results do not support a role for pathogenic IgA in canine PF.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/38820947/