Clinical-grade mesenchymal stem cells derived from umbilical cord improve septic shock in pigs

• Published in: Intensive care medicine experimental Vol. 6; no. 1; pp. 24 - 14
• Main Authors: Laroye, Caroline, Lemarié, Jérémie, Boufenzer, Amir, Labroca, Pierre, Cunat, Lisiane, Alauzet, Corentine, Groubatch, Frédérique, Cailac, Clémence, Jolly, Lucie, Bensoussan, Danièle, Reppel, Loïc, Gibot, Sébastien
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 08.08.2018; Springer Nature B.V; Springer; SpringerOpen
• Subjects: Clinical-grade; Critical Care Medicine; Hogs; Intensive; Intensive care; Life Sciences; Medicine; Medicine & Public Health; Mesenchymal stem cells; Sepsis; Septic shock; Stem cells; Umbilical cord; Septic shock; Umbilical cord; Clinical-grade; Mesenchymal stem cells
• ISSN: 2197-425X; 2197-425X
• DOI: 10.1186/s40635-018-0194-1

Background Septic shock is the leading cause of death in intensive care units. The pathophysiological complexity of this syndrome contributes to an absence of specific treatment. Several preclinical studies in murine models of septic shock have shown improvements to organ injury and survival after administration of mesenchymal stem cells (MSCs). To better mimic a clinical approach in humans, we investigated the impact of randomized controlled double-blind administration of clinical-grade umbilical cord-derived MSCs to a relevant pig model of septic shock. Methods Septic shock was induced by fecal peritonitis in 12 male domestic pigs. Animals were resuscitated by an experienced intensivist including fluid administration and vasopressors. Four hours after the induction of peritonitis, pigs were randomized to receive intravenous injection of thawed umbilical cord-derived MSCs (UCMSC) (1 × 10 6 UCMSCs/kg diluted in 75 mL hydroxyethyl starch (HES), ( n  = 6) or placebo (HES alone, n  = 6). Researchers were double-blinded to the treatment administered. Hemodynamic parameters were continuously recorded. Gas exchange, acid-base status, organ function, and plasma cytokine concentrations were assessed at regular intervals until 24 h after the onset of peritonitis when animals were sacrificed under anesthesia. Results Peritonitis induced profound hypotension, hyperlactatemia, and multiple organ failure. These disorders were significantly attenuated when animals were treated with UCMSCs. In particular, cardiovascular failure was attenuated, as attested by a better mean arterial pressure and reduced lactatemia, despite lower norepinephrine requirements. As such, UCMSCs improved survival in this very severe model (60% survival vs. 0% at 24 h). Conclusion UCMSCs administration is beneficial in this pig model of polymicrobial septic shock.