BonHanZA
In 2022, we have founded a Swiss-German study group that focuses on clinical and experimental ARDS research (termed BonHanZA based on the involved University Hospitals in Bonn, Hannover and Zurich).
More InformationOur group at the Institute of Intensive Care Medicine (IFI) has a translational research interest from bench to bedside.
The experimental focus of this group lies on endothelial permeability, injury to the glycocalyx and microcirculatory dysfunction in any critical illness. Over the last years our group has been focusing on blood purification techniques in particular on therapeutic plasma exchange in septic shock and we are currently planning a large international multicenter RCT (EXCHANGE-2).
Experimental
Clinical
In 2022, we have founded a Swiss-German study group that focuses on clinical and experimental ARDS research (termed BonHanZA based on the involved University Hospitals in Bonn, Hannover and Zurich).
More InformationWe are interested in molecular mechanisms regulating endothelial barrier function in response to inflammation. We have been focusing on the Angiopoietin (Angpt) / Tie2 ligand receptor system over the last decade. Tie2 is a transmembrane receptor tyrosine kinase that is essential for embryonic vessel development. In mature organisms, its function shifts toward maintenance of endothelial homeostasis and reaction to insults. Angpt-1 is the major circulating Tie2 agonist that promotes protective anti-permeability signals, whereas Angpt-2 has antagonistic properties. Our group was the first to prove in a murine knockout model that Angpt-2 directly contributes to sepsis morbidity and mortality.
Based on this finding we have conducted a series of experiments exploring potential therapeutic strategies (antibody, siRNA etc.) to eliminate or block the injurious Angpt-2 protein in sepsis models. We are also conducting drug-repurposing screens to identify potential off-target Angpt-2 regulators. Recently, we have gained much attention in the regulation of the Tie2 receptor expression per se and are currently working on the underlying mechanisms of posttranslational Tie2 modifications (Elife. 2020 Aug 24;9:e59520.). Dorothea and Mattia are working under
We are also interested in the interaction between endothelial cells and pericytes– both with regard to Angiopoietin signaling and the regulation of bioactive adrenomedullin (bioADM).
Another focus lies in the investigation of the endothelial glycocalyx both in vivo (SDF imaging) and in vitro (endothelial microperfusion chip model). As injury of the endothelial glycocalyx can be found early in critical illness and substantially contributes to endothelial dysfunction we investigate regulation of glycocalyx degradation both in septic shock as well as severe COVID-19 (Am J Respir Crit Care Med. 2020 Oct 15;202(8):1178-1181).
A major clinical research interest focuses on blood purification in sepsis and septic shock. In a prospective non-randomized pilot study, we could demonstrate that early therapeutic plasma exchange (TPE) improves hemodynamics and endothelial permeability as well as reduced inflammatory cytokines in patients with severe septic shock (EXCHANGE Pilot, Crit Care. 2018 Oct 30;22(1):285.). Recently, we finished a bicentric RCT with the University Hospital Bonn (Bode / Putensen) analyzing the role of PEX in septic shock on hemodynamic stability (EXCHANGE I, NCT04231994, Intensive Care Med. 2021 Jan 20. doi: 10.1007/s00134-020-06339-1). Funding for a multicenter RCT with a clinically meaningful endpoint is currently under review (EXCHANGE II).
We have built-up a biobank combining local and systemic biomaterials (bronchoalveolar lavage fluids (BALf) and blood) together with a thorough clinical characterization from ARDS patients in Hannover. This Sepsis and ARDS Register (termed SPARE-14) will help to translate experimental findings of our basic research group from bench to bedside. We are currently extending towards a second collection side at the USZ in Zurich.
Support of non-intubated patients with both chronic and acute lung failure with extra-corporeal membrane oxygenation, termed awake ECMO, is an innovative strategy that has been first implicated as ultra-protective approach to bridge end-stage lung disease patients to transplant without the injurious side effects of invasive ventilation. We continue to explore this strategy in selected patient cohorts such as patients with PcP associated ARDS (Crit Care. 2019 Dec 23;23(1):418.). ECMO support in special patient cohorts, e.g. patients with diffuse alveolar hemorrhage, and conditions, e.g. heparin free ECMO, are further clinical interests of our group.
We are also conducting research on extracorporeal cytokine removal in patients treated with CAR-T cells suffering from severe cytokine release syndrome (CytoreleaseEx, NCT04048434). This RCT has been initiated at Hannover and is currently extended to USZ, Zurich (financially supported by Cytosorbents).
Given our interest on plasma exchange and the observation that severe Covid-19 leads to a relative deficiency in the vWF cleaving protease (ADAMTS13) and coagulopathy we have applied for a biological proof of principle RCT in Zurich (PEXCoV, NCT04613986) (supported by Terumo and Octapharma).
Our experiments are currently supported by the „Schweizerischer Nationalfonds“ (SNF), „Deutsche Forschungsgemeinschaft“ (DFG), „Deutsches Zentrum Lungenforschung (DZL)”, and by unrestricted industrial grants from Cytosorbents, Terumo and Octapharma.
We are always looking for motivated people!
Please contact Sascha for further information (Sascha.david@usz.ch).