A bio‐artificial renal epithelial cell system conveys survival advantage in a porcine model of septic shock. (25th November 2014)

• Record Type: Journal Article
• Authors: Westover, Angela J.; Buffington, Deborah A.; Johnston, Kimberly A.; Smith, Peter L.; Pino, Christopher J.; Humes, H. David
• Is Part Of: Journal of tissue engineering and regenerative medicine. Volume 11:Number 3(2017)
• Page Start: 649
• Page End: 657
• Publication Date: 2014-11-25
• Subjects: artificial kidney -- capillary leak syndrome -- septic shock -- acute kidney injury -- tissue therapy -- immunotherapy -- systemic inflammatory response syndrome; Tissue engineering -- Periodicals; Regeneration (Biology) -- Periodicals; 610.28
• DOI: 10.1002/term.1961
• Languages: English
• ISSNs: 1932-6254

Abstract

Abstract: Renal cell therapy using the hollow fiber based renal assist device (RAD) improved survival time in an animal model of septic shock (SS) through the amelioration of cardiac and vascular dysfunction. Safety and ability of the RAD to improve clinical outcomes was demonstrated in a Phase II clinical trial, in which patients had high prevalence of sepsis. Even with these promising results, clinical delivery of cell therapy is hampered by manufacturing hurdles, including cell sourcing, large‐scale device manufacture, storage and delivery. To address these limitations, the bioartificial renal epithelial cell system (BRECS) was developed. The BRECS contains human renal tubule epithelial cells derived from adult progenitor cells using enhanced propagation techniques. Cells were seeded onto trabeculated disks of niobium‐coated carbon, held within cryopreservable, perfusable, injection‐moulded polycarbonate housing. The study objective was to evaluate the BRECS in a porcine model of SS to establish conservation of efficacy after necessary cell sourcing and design modifications; a pre‐clinical requirement to move back into clinical trials. SS was incited by peritoneal injection of E. coli simultaneous to insertion of BRECS (n=10) or control (n=15), into the ultrafiltrate biofeedback component of an extracorporeal circuit. Comparable to RAD, prolonged survival of the BRECS cohort was conveyed through stabilization of cardiac output and vascular leak. In conclusion, the demonstration of conserved efficacy with BRECS therapy in a porcine SS model represents a crucial step toward returning renal cell therapy to the clinical setting, initially targeting ICU patients with acute kidney injury requiring continuous renal replacement therapy. Copyright © 2014 John Wiley & Sons, Ltd.