BECAS
IVANOFF MARINOFF Ivana Mariel
congresos y reuniones científicas
Título:
Effects Of Aging In An Experimental Model Of Intestinal Transplantation. Preliminary Results
Autor/es:
GENTILINI MARÍA VIRGINIA; STRINGA PABLO; ARRIOLA CONSTANZA; LAUSADA NATALIA; MOREIRA JEREMÍAS; IVANOFF MARINOFF IVANA; RODRIGO PAPA-GOBBI; RUMBO MARTÍN; TULLIUS STEFAN; GONDOLESI GABRIEL
Lugar:
Mar Del Plata
Reunión:
Congreso; Reunión Anual de Sociedades de Biociencias SAI-SAIC-SAFIS 2022; 2022
Institución organizadora:
SAI - SAFIS - SAIC
Resumen:
Older transplant recipients experience increased incidence of in¬fection, malignancy, and death compared with younger patients, likely because of aging-associated immune senescence. Youthful allografts could theoretically drive rejuvenation, but the data are less clear. We aimed to evaluate the effects of aging in an experimental model of intestinal transplantation (ITx) Materials and Methods. In¬testinal allografts from young Sprague-Dawley rats were transplant¬ed in Wistar rats. Based on age of the recipient, two experimental groups were performed: 1-Old Recipient (OR, >9 months, n =4) and 2-Young Recipient (YR, 2 months, n =4). Intestinal graft and blood samples were collected at 30 minutes, 5, 7, 9 and 18 postopera¬tive days (POD) after ITx. Graft and recipient survival, histopatho¬logical analysis in search of acute cellular rejection (ACR) signs (Wu Score), intestinal absorptive capacity; Kinetics of CD4 and CD8 frequency (flow cytometry) were compared between groups. Also, donor specific allorecognition were evaluated by Mixed Lym-phocyte Reaction (MLR) assay (flow cytometry). Results: Despite the kinetic of histological ACR process was similar in both groups (mild to moderate at 7 POD, severe ACR at end-point), OR survived longer (OR: 14 vs YR: 8 POD) and showed lower percentage of body reduction than YR at the clinical endpoint (O: 20% vs Y: 25%). Glycemia curves were similar in both groups, demonstrating com¬parable graft absorptive capacity. During the ACR, a tendency to a reduction of CD4 (OR: 12% vs YR: 35%) and an increment in CD8 frequency (OR: 65% vs YR: 180%) in the gut was observed in both groups. Finally, a donor specific CD4 and CD8 allorecognition was demonstrated by MLR assays. Conclusion: Our preliminary results suggest that there is a difference in the ACR process depending on the recipient age. This study is currently being extended with a large number of animals.