Projects per year
Abstract
In pemphigoid diseases, direct immunofluorescence can be used to differentiate 2 patterns of antibody deposition at the dermal-epidermal junction; u- and n-serrated pattern. The u-serrated pattern is found in epidermolysis bullosa acquisita, and n-serrated pattern in all other pemphigoid diseases. To determine the detection frequency of these serrated patterns and the optimal thickness of biopsy cryosections, 2 patient cohorts obtained form our routine autoimmune laboratory were analysed; a retrospective cohort (n = 226) and a prospective cohort (n = 156). In 76% (291/382) of biopsies, a pattern was recognized, of which 96% (278/291) and 4% (13/291) had an n- or u-serrated pattern, respectively. A u-serrated pattern was seen in all epidermolysis bullosa acquisita biopsies confirmed by serology. No antibodies against type VII collagen were detected in any of the sera from biopsies with nserrated pattern. No differences between the detection frequencies of serrated pattern were seen with respect to age, sex, biopsy site, or section thickness, while the detection frequency was higher in patients with serum anti-BP180 reactivity compared with those without. In conclusion, serrated pattern analysis using direct immunofluorescence has a high detection frequency and specificity for epidermolysis bullosa acquisita and will further facilitate the diagnosis of latter disorder.
Original language | English |
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Article number | adv00410 |
Journal | Acta Dermato-Venereologica |
Volume | 101 |
Issue number | 3 |
Pages (from-to) | adv00410 |
ISSN | 0001-5555 |
DOIs | |
Publication status | Published - 03.2021 |
Research Areas and Centers
- Academic Focus: Center for Infection and Inflammation Research (ZIEL)
- Centers: Center for Research on Inflammation of the Skin (CRIS)
DFG Research Classification Scheme
- 204-05 Immunology
- 205-19 Dermatology
- 205-32 Medical Physics, Biomedical Engineering
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EXC 2167: Precision Medicine in Chronic Inflammation (PMI)
Schreiber, S., Baines, J. F., Bosch, T. C. G., Buyx, A., Erdmann, J., Franke, A., Huber, R., Klein, C., Köhl, J., König, I. R., Lange, C., Laudes, M., Lieb, W., Ludwig, R., Nebel, A., Niemann, S., Rabe, K. F., Riemekasten, G., Rose-John, S., Rosenstiel, P. C., Schulenburg, H., Schwarz, K., Traulsen, A., Weidinger, S. & Zillikens, D.
01.01.19 → …
Project: DFG Projects › DFG Cluster of Excellence
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CRU 303: Pemphigoid Diseases - Molecular Pathways and their Therapeutic Potential
Sadik, C., Zillikens, D., Ibrahim, S., Baines, J. F., Schmidt, E., Köhl, J., Ehlers, M., Hirose, M., König, P., Ludwig, R., Manz, R., Schwaninger, M., Beek, N., Erdmann, J., König, I. R., Verschoor, A., Karsten, C., Bieber, K. & Busch, H. S.
01.04.15 → 31.12.23
Project: DFG Projects › DFG Joint Research: Research Units/Clinical Research Units