Elias Walter

Dr. Elias Walter


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2016 in Journal of Investigative Dermatology
Verified
Journal Article
Closed access
VRVera Rötzer
Vera Rötzer
EHEva Hartlieb
Eva Hartlieb
JWJulia Winkler
Julia Winkler
EWElias Walter
Elias Walter
ASAngela Schlipp
Angela Schlipp
JWJens Waschke
Jens Waschke

15 June 2017 in Scientific Reports
Verified
Journal Article
Open access
PDF file
EWElias Walter
Elias Walter
FVFranziska Vielmuth
Franziska Vielmuth
LRLukas Rotkopf
Lukas Rotkopf
MSMiklós Sárdy
Miklós Sárdy
OHOrsolya N. Horváth
Orsolya N. Horváth
JWJens Waschke
Jens Waschke
Pemphigus is an autoimmune blistering skin disease caused primarily by autoantibodies against desmoglein (Dsg)1 and 3. Here, we characterized the mechanisms engaged by pemphigus IgG from patients with different clinical phenotypes and autoantibody profiles. All pemphigus vulgaris (PV) and pemphigus foliaceus (PF) IgG and AK23, a monoclonal mouse antibody against Dsg3, caused loss of cell cohesion, cytokeratin retraction and p38MAPK activation. Strong alterations in Dsg3 distribution were caused by mucosal (aDsg3 antibodies), mucocutaneous (aDsg1 + aDsg3) as well as atypical (aDsg3) PV-IgG. All PV-IgG fractions and AK23 compromised Dsg3 but not Dsg1 binding and enhanced Src activity. In contrast, rapid Ca2+ influx and Erk activation were induced by mucocutaneous PV-IgG and pemphigus foliaceus (PF) IgG (aDsg1) whereas cAMP was increased by mucosal and mucocutaneous PV-IgG only. Selective inhibition of p38MAPK, Src or PKC blocked loss of keratinocyte cohesion in response to all autoantibody fractions whereas Erk inhibition was protective against mucocutaneous PV-IgG and PF-IgG only. These results demonstrate that signaling patterns parallel the clinical phenotype as some mechanisms involved in loss of cell cohesion are caused by antibodies targeting Dsg3 whereas others correlate with autoantibodies against Dsg1. The concept of key desmosome regulators may explain observations from several experimental models of pemphigus.

1 January 2018 in Journal of Investigative Dermatology
Verified
Journal Article
Closed access
FVFranziska Vielmuth
Franziska Vielmuth
MWMarie-Therès Wanuske
Marie-Therès Wanuske
MRMariya Y. Radeva
Mariya Y. Radeva
MHMatthias Hiermaier
Matthias Hiermaier
DKDaniela Kugelmann
Daniela Kugelmann
VSVolker Spindler
Volker Spindler

21 July 2023 in Journal of Periodontology
Verified
Journal Article
Open access
NWNils Werner
Nils Werner
KHKatrin Heck
Katrin Heck
EWElias Walter
Elias Walter
CEChristina Ern
Christina Ern
CBCaspar Victor Bumm
Caspar Victor Bumm
MFMatthias Folwaczny
Matthias Folwaczny
Background: To investigate tooth‐related factors that influence the reduction of probing pocket depths (PPD) after non‐surgical periodontal therapy (NST).Methods: Seven hundred forty‐six patients with a total of 16,825 teeth were included and retrospectively analyzed. PPD reduction after NST was correlated with the tooth‐related factors; tooth type, number of roots, furcation involvement, vitality, mobility, and type of restoration; using logistic multilevel regression for statistical analysis.Results: NST was able to reduce probing depth overall stratified probing depths (1.20 ± 1.51 mm, p ≤ 0.001). The reduction was significantly higher at teeth with higher probing depths at baseline. At pockets with PPD ≥ 6 mm, PPD remains high after NST. Tooth type, number of roots, furcation involvement, vitality, mobility, and type of restoration are significantly and independently associated with the rate of pocket closure.Conclusions: The tooth‐related factors: tooth type, number of roots, furcation involvement, vitality, mobility, and type of restoration had a significant and clinically relevant influence on phase I and II therapy. Considering these factors in advance may enhance the prediction of sites not responding adequately and the potential need for additional treatment, such as re‐instrumentation or periodontal surgery, to ultimately achieve the therapy end points.

19 June 2019 in British Journal of Dermatology
Verified
Journal Article
Closed access
PDF file
DED. T. Egu
D. T. Egu
ASA. M. Sigmund
A. M. Sigmund
ESE. Schmidt
E. Schmidt
VSVolker Spindler
Volker Spindler
EWElias Walter
Elias Walter
JWJ. Waschke
J. Waschke