2011 - ISBTS 2011 Symposium


This page contains exclusive content for the member of the following sections: TTS, ITA. Log in to view.

Plenary Session II: Physiology & Mucosal Biology + Oral Communications 8

10.207 - Single center experience: Mesenchymal stem cell (MSCs) therapy in patients with small bowel transplantation

Presenter: Selcuk, Kilinc, ISTANBUL, Turkey
Authors: Selcuk Kilinc1

207
Single center experience: Mesenchymal stem cell (MSCs) therapy in patients with small bowel transplantation

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:

  1. A Pascher, S Kohler, P Neuhaus, J Practscke Present status and future perspective of intestinal transplantation. European Society For Org Transplantation 21(2008) 401-414
  2. Zhang X, Jiao C, Zhao S Role of mesenchymal stem cells in immunological rejection of organ  transplantation. Stem Cell Rev. 2009 Dec; 5(4): 402-9
  3. Popp FC, Eggenhofer E, Renner P, Slowik P, Lang SA, Kaspar H et al. Mesenchymal stem cells can induce long-term acceptance of solid organ allografts in synergy with low-dose mycophenolate Transpl Immunol. 2008 Nov; 20 (1-2): 55-60
  4. English K, French A, Wood KJ Mesenchymal stromal cells: facilitators of successful transplantation?.Cell Stem Cell 2010 Oct 8; 7(4): 431-42.
  5. Christ B, Dollinger MM. The generation of hepatocytes from mesenchymal stem cells and engraftment into the liver. Curr Opin Organ Transplant. 2010 Dec 9.
  6.  Lin H, Xu R, Zhang Z, Chen L, Shi M, Wang FS Implications of the immunuregulatory functions of mesenchymal  stem cells in the treatment of human liver diseases. Cell Mol Immunol. 2010 Jan; 8(1): 19-22. Epub 2010 Nov 22. 

Important Disclaimer

By viewing the material on this site you understand and accept that:

  1. The opinions and statements expressed on this site reflect the views of the author or authors and do not necessarily reflect those of The Transplantation Society and/or its Sections.
  2. The hosting of material on The Transplantation Society site does not signify endorsement of this material by The Transplantation Society and/or its Sections.
  3. The material is solely for educational purposes for qualified health care professionals.
  4. The Transplantation Society and/or its Sections are not liable for any decision made or action taken based on the information contained in the material on this site.
  5. The information cannot be used as a substitute for professional care.
  6. The information does not represent a standard of care.
  7. No physician-patient relationship is being established.

Social

Contact

Staff Directory
+1-514-874-1717
info@tts.org

Address

The Transplantation Society
International Headquarters
740 Notre-Dame Ouest
Suite 1245
Montréal, QC, H3C 3X6
Canada