Pemphigus vulgaris (PV) is an autoimmune bullous disease of the skin and mucous membranes characterized by the presence of circulating and tissue-bound autoantibodies against keratinocyte cell surface antigens, specifically desmoglein (Dsg) 1 and 3. The pathogenic role of anti-Dsg antibodies is well-established, while the mechanism of blister formation is only partly defined. We have applied a previously developed method for the efficient immortalization of IgG+ memory B cells to identify novel target antigens in PV. A human monoclonal antibody reactive with a hitherto unreported non-Dsg antigen was isolated. Immunoprecipitation and immunoblotting studies with keratinocyte extracts indicated α-catenin as the putative antigen, then confirmed by immunoblotting on the recombinant protein. Four of ten PV sera reacted with recombinant α-catenin. Although the isolated human monoclonal antibody was unable to dissociate keratinocyte monolayers and also to synergize with a pathogenic antibody , further studies are warranted to assess its possible contribution in the multifactorial pathogenesis and heterogeneous manifestations of PV disease.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593111PMC
http://dx.doi.org/10.3389/fimmu.2019.01391DOI Listing

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