Journalartikel
Autorenliste: Hudemann, Christoph; Exner, Yvonne; Pollmann, Robert; Schneider, Karina; Zakrzewicz, Anna; Feldhoff, Simon; Schmidt, Thomas; Spindler, Volker; Rafei-Shamsabadi, David; Völlner, Frauke; Waschke, Jens; Tikkanen, Ritva; Hertl, Michael; Eming, Rüdiger
Jahr der Veröffentlichung: 2023
Seiten: 254-25+
Zeitschrift: Journal of Investigative Dermatology
Bandnummer: 143
Heftnummer: 1
ISSN: 0022-202X
eISSN: 1523-1747
Open Access Status: Bronze
DOI Link: https://doi.org/10.1016/j.jid.2022.07.030
Verlag: Elsevier
Abstract:
Pemphigus vulgaris is a severe autoimmune blistering disease characterized by IgG autoantibodies (auto-abs) against the desmosomal adhesion molecules desmoglein (DSG) 3 and DSG1. Underlying mechanisms leading to blister formation upon binding of DSG-specific IgG auto-abs are not fully understood. Numerous studies showed the pathogenicity of IgG auto-ab binding to the aminoterminal region 1 (EC1) of the DSG3 ectodomain. However, auto-abs in pemphigus vulgaris are polyclonal, including IgG against both aminoterminal- and membrane-proximal epitopes of the DSG3 ectodomain. In this study, the pathogenicity of a previously uncharacterized murine monoclonal IgG antibody, 2G4, directed against the membrane-proximal region (EC5) of the DSG3 ectodomain was characterized and tested in various specificity and functionality assays. The results clearly show that 2G4 is capable of inhibiting intercellular keratinocyte adhesion and of inducing cellular DSG3 redistribution by activation of the p38MAPK signal transduction pathway. In this study, we provide evidence that an IgG auto-abs directed against the membrane-proximal region EC5 of DSG3 induces acantholysis, the hallmark in pemphigus vulgaris. These findings challenge the current concept that IgG auto-abs targeting the NH2-terminal portion of the DSG3 ectodomain are pathogenic only. Our study provides further aspects for a deeper understanding of desmosomal keratinocyte adhesion and improves our insight into the complex autoab-induced blister formation in pemphigus vulgaris.
Zitierstile
Harvard-Zitierstil: Hudemann, C., Exner, Y., Pollmann, R., Schneider, K., Zakrzewicz, A., Feldhoff, S., et al. (2023) IgG against the Membrane-Proximal Portion of the Desmoglein 3 Ectodomain Induces Loss of Keratinocyte Adhesion, a Hallmark in Pemphigus Vulgaris, Journal of Investigative Dermatology, 143(1), pp. 254-25+. https://doi.org/10.1016/j.jid.2022.07.030
APA-Zitierstil: Hudemann, C., Exner, Y., Pollmann, R., Schneider, K., Zakrzewicz, A., Feldhoff, S., Schmidt, T., Spindler, V., Rafei-Shamsabadi, D., Völlner, F., Waschke, J., Tikkanen, R., Hertl, M., & Eming, R. (2023). IgG against the Membrane-Proximal Portion of the Desmoglein 3 Ectodomain Induces Loss of Keratinocyte Adhesion, a Hallmark in Pemphigus Vulgaris. Journal of Investigative Dermatology. 143(1), 254-25+. https://doi.org/10.1016/j.jid.2022.07.030
Schlagwörter
AUTOANTIBODIES; CELL-ADHESION; INVOLVEMENT; MONOCLONAL-ANTIBODY; P38MAPK; PROTEIN-KINASE-C