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Biology subjects

Artzy-Schnirman, A.

Publications and source records attributed to Artzy-Schnirman, A..

3 recordsLinked to original sources

iPSCs-derived Bronchial Airways-On-Chip for Assessment of Cytokine Secretion triggered by Volatile Organic Compounds

Air quality monitoring currently relies mostly on a combination of epidemiological data and classic experimental data. Our objective was to design an alternative approach for assessing air pollutant risk potential using a specialized platform capable of detecting long-term and indirect effects of exposure via the inhaled route. We used a Bronchial Airways-On-Chip (BOC) offering some of the physiological complexity of the human lung based on our previously developed device coupled with in-vitro differentiated bronchial epithelium derived from induced Pluripotent Stem Cells (iPSCs). This setup is capable of replicating bronchial epithelia exposure to irritants at air-liquid interface, in controlled and reproducible conditions. It comprises the first proof-of-concept design combining a BOC with iPSCs-derived bronchial epithelium as an alternative approach towards potential risk assessmnet of inhaled pollutants. As a representative pollutant we use Benzene, a Volatile Organic Compound (VOC). At low concentrations and short-term exposure it is not considered acutely harmful, but long-term exposure can result in mutagenic and carcinogenic effects. As air pollutant toxicity is known to be mediated by the respiratory epithelial lining and secretion of cytokines, we demonstrate our system to be sufficiently sensitive to capture increased cytokine secretion corresponding to increasing concentrations of Benzene. Of utmost relevance is our finding that an accumulative effect could be detected, only caused by prolonged exposure at low concentrations of Benzene, previously shown to be non-toxic in classic short-term in-vitro studies. Finally, the accumulative effect could be reversed using a commonly-used asthma medication (Montelukast), further supporting the relevance of the setup.

bioengineering↗

Ventilation-induced epithelial injury drives biological onset of lung trauma in vitro and is mitigated with anti-inflammatory therapeutics

Mortality rates among patients suffering from acute respiratory failure remain perplexingly high despite maintenance of blood homeostasis. The biotrauma hypothesis advances that mechanical forces from invasive ventilation trigger immunological factors that spread systemically. Yet, how these forces elicit an immune response remains unclear. Here we show that flow-induced stresses under mechanical ventilation can injure the bronchial epithelium of ventilated in vitro upper airway models and directly modulate inflammatory cytokine secretion associated with pulmonary injury. We identify site-specific susceptibility to epithelial erosion in airways from jet-flow impaction and measure an increase in cell apoptosis and modulated secretions of cytokines IL-6, 8 and 10. We find that prophylactic pharmacological treatment with anti-inflammatory therapeutics reduces apoptosis and pro-inflammatory signaling during ventilation. Our 3D in vitro airway platform points to a previously overlooked origin of lung injury and showcases translational opportunities in preclinical pulmonary research towards protective therapies and improved protocols for patient care.

bioengineering↗

Artificial Antigen Presenting Cells for Detection and Desensitisation of Auto-reactive T cells Associated with Type 1 Diabetes

Autoimmune diseases and in particular type 1 diabetes rely heavily on treatments that target the symptoms rather than prevent the underlying disease. One of the barriers to better therapeutic strategies is the inability to detect and efficiently target rare autoreactive T-cell populations that are major drivers of these conditions. Here, we develop a unique artificial antigen presenting cell (aAPC) system from biocompatible polymer particles that allows specific encapsulation of bioactive ingredients. Using our aAPC we demonstrate that we are able to detect rare autoreactive CD4 populations in human patients and using mouse models we demonstrate that our particles are able to induce desensitization in the autoreactive population. This system provides a promising tool that can be used in the prevention of autoimmunity before disease onset.

bioengineering↗