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Third Party Mesenchymal Stromal Cell Infusion in Kidney Transplant Recipient: 6-Month Safety Interim Analysis

L. Weekers,1 P. Erpicum,1 O. Detry,3 C. Lechanteur,2 E. Baudoux,2 F. Jouret,1 Y. Beguin.2

1Nephrology, University Hospital of Liege, Liege, Belgium
2Hematology, University Hospital of Liege, Liege, Belgium
3Abdominal Surgery, University Hospital of Liege, Liege, Belgium.

Meeting: 2015 American Transplant Congress

Abstract number: B55

Keywords: Immunosuppression, Kidney transplantation, Stem cells

Session Information

Session Name: Poster Session B: Cell Transplantation and Cell Therapies

Session Type: Poster Session

Date: Sunday, May 3, 2015

Session Time: 5:30pm-6:30pm

 Presentation Time: 5:30pm-6:30pm

Location: Exhibit Hall E

Back-ground

Mesenchymal stromal cell (MSC) have immunomodulating properties and could be used as immunosuppressive agents.

We report the 6-month safety results for the 5 first patients treated with MSC after kidney transplantation (KTx). Here, we address 3 specific safety issues:

– Immunization against MSC

– Engraftment syndrome defined as acute graft dysfunction not related to rejection

– Over-immunosuppression.

Patients and method

MSC production was carried out locally. MSC were not matched with kidney recipients' HLA. Included patients were non-immunized, first transplant recipient from deceased donors. MSC (1.5 – 3.0 x 106/kg) infusion was planned 3 to 5 days post KTx. Patients with cardiovascular instability post KTx were excluded. All patients were treated with Basiliximab induction, Tacrolimus, Mycophenolate Mofetil and Steroid. We prospectively screened for anti-HLA antibodies at month 1, 3 and 6. Informed consent was obtained from all participants. The local ethical committee approved the protocol.

Results

Collectively there were 23/50 and 29/50 HLA mismatches (MM) with kidney and MSC donor respectively, out of which 5 were shared MM.

Baseline characteristics
Recipient Age at Tx (years) 63 ± 6
  Gender (M/F) 4/1
  BMI (kg/m2) 27 ± 3
  Dialysis vintage (days) 373 ± 564
Kidney donor Age (years) 51 ± 18
  Gender (M/F) 3/2
  BMI (kg/m2) 26 ± 5
  DBD/DCD 4/1
Transplantation CIT (min) 737 ± 219
  WIT (min) 46 ± 16
  HLA mismatches (n)  
  A (0/1/2) 0/5/0
  B (0/1/2) 1/4/0
  Cw (0/1/2) 1/3/1
  DR (0/1/2) 1/4/0
  DQ (0/1/2)  
MSC donor HLA mismatches (n)  
  A (0/1/2) 1/2/2
  B (0/1/2) 1/3/1
  Cw (0/1/2) 0/4/1
  DR (0/1/2) 1/3/1
  DQ (0/1/2) 0/3/2
DB/CD: donor after brain /cardiac -death; C/WIT: cold/warm ischemic time

One patient developed de novo DSA, 2 patients anti-HLA antibodies against shared kidney/MSC MM and 1 patient developed 2 specific antibodies against MSC (MSCSA) at month 6. All antibodies were anti HLA class I except for 1.

We did not observe any “engraftment” syndrome.

Three patients experienced non-severe opportunistic infections: 1 CMV reactivation and 2 polyoma-BK virus viremia.

Conclusion

We did not observe any strong safety signal. We did however observe some degree of immunization in 3 patients: 2 developed antibodies against shared kidney/MSC donor HLA MM and 1 MSCSA.

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To cite this abstract in AMA style:

Weekers L, Erpicum P, Detry O, Lechanteur C, Baudoux E, Jouret F, Beguin Y. Third Party Mesenchymal Stromal Cell Infusion in Kidney Transplant Recipient: 6-Month Safety Interim Analysis [abstract]. Am J Transplant. 2015; 15 (suppl 3). https://atcmeetingabstracts.com/abstract/third-party-mesenchymal-stromal-cell-infusion-in-kidney-transplant-recipient-6-month-safety-interim-analysis/. Accessed May 15, 2025.

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