Effect of polyethylene glycol in pig intestinal allotransplantation without immunosuppression
- Others:
- Pôle Digestif, Unité de Support Nutritionnel et de Greffes Intestinales ; Centre Hospitalo-Universitaire
- Service de Chirurgie Digestive / Centre de Transplantation Hépatique [CHU Nice] ; Centre Hospitalier Universitaire de Nice (CHU Nice)
- U576, Faculté de Médecine ; Institut National de la Santé et de la Recherche Médicale (INSERM)
- Transport ionique aspects normaux et pathologiques ; Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)
- Service d'anatomopathologie, Université Paris V ; CHU Necker - Enfants Malades [AP-HP] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
- Génétique Animale et Biologie Intégrative (GABI) ; Institut National de la Recherche Agronomique (INRA)-AgroParisTech
- Laboratoire d'Immunologie, Hôpital de l'Archet 2 ; Centre Hospitalo-Universitaire
Description
Objectives: We evaluated whether IGL-1, a graft preservation solution containing polyethylene glycol, improves the outcome of small bowel grafts in comparison to the University of Wisconsin (UW) solution in a pig allotransplantation model.[br/] Materials and Methods: Seventeen pigs were randomly allocated to group 1 (n = 10; intestinal allotransplantation with IGL-1) and group 2 (n = 7; allotransplantation with UW). Pigs received no immunosuppression and were sacrificed on postoperative d (POD) 8. Intestinal specimens were obtained from the animal immediately before cold flushing (T0), 2 h after graft reperfusion (T1), and at sacrifice (T2).[br/] Results: Survival rate to POD 8 was 50% in group 1 compared with 16% in group 2 (P < 0.05); 62% of pigs in group 1 did not present any acute cellular rejection (ACR) compared to 16% in group 2 (P < 0.05). Severe ACR rate was 25% in group 1 and 66% in group 2 (P < 0.05). iNOS activity and intestinal caspase 3 levels increased significantly between T0 and T1 in group 1 compared to group 2 (P < 0.05). Cell necrosis increased significantly between TO and T1 in group 2 compared with group 1 (P < 0.05) whereas cell apoptosis was significantly higher at T1 compared with T0 in group 1 in comparison to group 2.[br/] Conclusions: Our results show that IGL-1 improves intestinal graft viability as compared to UW solution, possibly by reducing graft immunogenicity and by favoring intestinal epithelial repair.
Abstract
Chantier qualité GA
Additional details
- URL
- https://hal.science/hal-01000002
- URN
- urn:oai:HAL:hal-01000002v1
- Origin repository
- UNICA