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Table 2 Use of MSCs to promote engraftment in large animal models

From: Mesenchymal stromal cells to modulate immune reconstitution early post-hematopoietic cell transplantation

HSC source

Model

Conditioning; Immune suppression

MSC source

MSC dose

Outcome

Ref

Human CD34+BM cells

Fetal sheep xenograft

None; n/a

Human autologous & allogeneic BM

5 × 104 - 7.5 × 105

Increased engraftment in PB and BM, no difference between autologous & allogeneic

16

Haploidentical BM cells

Canine

9.2 Gy; n/a

Allogeneic BM (3rd party), immortalized clonal populations or primary MSC culture

3 dosing schedules: 30 × 106/kg 3×/wk ×1 wk, then 2×/wk; 15 × 106/kg 5×/wk; 1 × 106/kg 3×/wk

No effect; 50 % graft rejection & 50 % fatal acute GVHD

26

DLA-identical BM cells

Canine

1 Gy; MMF and CSA

Donor-derived BM

1.2 - 1.8 × 106/kg day 0, 1.1 - 1.3 × 106/kg day 35

No effect, uniform graft rejection at median of 8 weeks after initial donor engraftment

27

Autologous CD34+ BM cells (intra-BM)

Nonhuman primate

5.5 Gy ×2 doses or Bu; n/a

Autologous BM

NR

1.6-6 fold increase in donor CFUs in BM

28

  1. MSCs indicates mesechymal stromal cells, HSC hematopoietic stem cells, BM bone marrow, PB peripheral blood, Gy gray, Bu busulfan, NR not reported, CFUs colony-forming units, wk week, GVHD graft-versus-host disease, DLA dog leukocyte antigen, MMF mycophenolate mofetil, CSA cyclosporine