This page contains exclusive content for the member of the following sections: TTS, ITA. Log in to view.
                    Presenter: Selcuk, Kilinc, ISTANBUL, Turkey
                    Authors: Selcuk Kilinc1
                
Selcuk Kilinc
Tepecik Training and Research Hospital, Izmir, Turkey
Introduction: Acute cellular rejection (ACR) occurs more frequently and severely in the small intestinal graft than in any other abdominal organ. (1)MSCs are able to inhibit T cell proliferation in vitro and in vivo and exert similar inhibitory effects on B, dendritic, and natural killer cells as a new stem cell therapy class for autoimmune disease, solid organ transplantation and treatment of graft-versus-host disease (GVHD). (2,3,4) Severe liver dysfunction and fibrosis is another problem. MSCs can produce a series of growth factors, enhance hepatocyte functionality and stimulate endogenous hepatocyte proliferation .(5,6)
Aim: We describe three patients with intestinal failure treated by small bowel (SB) tx and MCSs andanalyze these patients’ prognosis and follow-up.
Ethics committee: Republic of Turkey Ministry of Health permission granted.
Discussion: Property and treatment modality of cases seen in table.
The aim in all cases was for a first dose of at least 1 million/kg to be given from the transplanted organ SMA, and for a second dose to be given by catheter inserted 15 days postoperatively. The absence of rejection in Case 2 may be attributed to the different method of administration.This could not be done in two cases that died for various reasons as detailed respectively: Incompatibilities between suitable cadaver donor harvesting time and MSCs of adequate maturity being obtained ; inability to take samples containing sufficient qualification from bone marrow as a result of clinical failures in the patient due to undergo small bowel transfer ;inability to administer first dose of MSCs on day 0 postoperatively due to incompatibility in cadaveric donor and recipient blood crosses.
So we newly designed phase 2 clinical study (30 cases) and the requisite permissions have been obtained.
Table: Immunosupressive treatment and property of cases
| 
				 
  | 
			
				 Age/ Gender  | 
			
				 Diagnosis  | 
			
				 HLA  | 
			
				 Donor HLA  | 
			
				 Tx time  | 
			
				 Donor  | 
			
				 MSCs  | 
			
				 IR  | 
			
				 ACR time  | 
			
				 Follow-up  | 
		
| 
				 Case 1  | 
			
				 25/F  | 
			
				 Total intestinal resection due to mesenteric artery ischemia in gestation (8 week)  | 
			
				 A 02/24 B 59 DR 02/30  | 
			
				 A02/30 B3/58 DR03/07  | 
			
				 1 yr after resection  | 
			
				 Cadaveric SBTx  | 
			
				 1st dose: 1x106 per kg by subclavian vein , 1 week before SBTx 2nd: dose 2 weeks after SBTx by same dose via intra venous route  | 
			
				 ATG Steroid, FK 506,  | 
			
				 13 days later, severe  | 
			
				 Ex 18th day ( severe rejection,sepsis)  | 
		
| 
				 Case 2  | 
			
				 12/F  | 
			
				 Total intestinal resection due to mesenteric artery trauma  | 
			
				 A 02/24 B 08/51 DRB1 3/13  | 
			
				 A 02/24 B12/44 DB 1 3 
  | 
			
				 1 yr later  | 
			
				 Cadaveric SBTx  | 
			
				 2 doses: 1st dose: 1x106 per kg via superior mesenteric artery catheter at time of operation 2nd: same dose by intra venous route  | 
			
				 ATG Steroid, FK 506, Sirolimus,  | 
			
				 1 mo later mildly  | 
			
				 Lived (1 yr) TPN deseaced at 3th mo  | 
		
| 
				 Case 3  | 
			
				 45/ M  | 
			
				 Total intestinal resection and hemi-colectomia due to mesenteric arter ischemia  | 
			
				 A26 B 08 DRB1 /04  | 
			
				 A02/02 B40/51 DR03/15  | 
			
				 1 month after resection  | 
			
				 Cadaveric SBTx  | 
			
				 
 1st dose 0,5x106 per kg via portal vein 1 day before SBTx 2nd dose: Can’t administration  | 
			
				 ATG Steroid, FK 506,  | 
			
				 Severe, 2 mo later  | 
			
				 Ex, at 67 days (severe rejection,sepsis)  | 
		
IR:Immunosuppressive regimen, ATG: Anti thymocyte globulin, TPN: Total parenteral nutrition
Literature:
By viewing the material on this site you understand and accept that:
The Transplantation Society
International Headquarters
740 Notre-Dame Ouest
Suite 1245
Montréal, QC, H3C 3X6
    Canada
Используйте Вавада казино для игры с бонусом — активируйте промокод и начните выигрывать уже сегодня!