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. Author manuscript; available in PMC: 2015 Mar 1.
Published in final edited form as: Bone Marrow Transplant. 2014 Jul 21;49(9):1198–1204. doi: 10.1038/bmt.2014.137

TABLE 1.

DLA-nonidentical marrow transplantation after ECP ± pentostatin and 920cGy with postgrafting MTX

Recipient Dog # Buffy Coat TNCs × 108/kg Marrow TNCs × 108/kg Neutrophil Increasec % Donor MNC Chimerism (Max-final) Rejection GVHDd Survival (days) Cause of Death
Group A1a E981 4.3 1.9 Yes 100-100 No S/G/L 17 GVHDe
G120* 3.9 2.2 Yes 36 No S/G/L 16 GVHDe
G113 6.9 3.4 Yes 100-0 Yes L 50 End of study
G066 6.8 6.1 Yes 100-100 No S/G/L 19 GVHDe
G170 2.3 2.8 No 67–100 No G/L 20 GVHDe
Group A2b G077 2.1 3 No 41–73 No N 9 Herpes infectione
G088 2.2 3.1 Yes 95–100 No S/G/L 22 GVHDe
G095 1.8 2.7 No 71-0 Yes N 22 End of Study
G227 1.2 2.9 No 74 No S/G/L 10 GVHDe

Dogs given marrow grafts and additional donor PBMC from DLA-nonidentical littermates after conditioning with 920 cGy TBI and post grafting immunosuppression with methotrexate

DLA-nonidentical dogs given marrow grafts, extracorporeal photopheresis (ECP) product, pentostatin, and donor buffy coat cells after conditioning with 920 cGy total body irradiation (TBI) and postgrafting immunosuppression with methotrexate (MTX).

a

Dogs in group A1 received ECP product on days −2 and −1; 920 cGy TBI on day 0; donor buffy coat cells on days 1 and 2; MTX (0.4 mg/kg i.v. on days 1,3, 6, 11, and then weekly thereafter until day 102.

b

Dogs in group A2 received ECP product on days −6 and −5; 4 mg/m2 pentostatin i.v. on days −4, and −3; 920 cGy TBI on day 0; buffy coat and MTX regimen as in group A1.

c

Absolute neutrophil count increase greater than 500/μL.

d

S=skin; G=gut; L=liver.

e

Dogs were euthanized because of poor condition.

*

No DNA sample was obtained on day 7 after HCT.