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. Author manuscript; available in PMC: 2013 Oct 25.
Published in final edited form as: Transplantation. 2002 Sep 27;74(6):10.1097/01.TP.0000028779.24725.CF. doi: 10.1097/01.TP.0000028779.24725.CF

Table 1.

The contributions of CDC in the context of the potent tolerizing effects of DST plus anti-CD154 mAb treatment regimen in recipients of islet allografts

Donor Recipients Treatment Graft survival
DBA/2 B6AF1 untreated 9, 11, 13, 15, 17
DBA/2 B6AF1 DSTa + MR1b >150 n=10
DBA/2 B6AF1 DSTa + MR1b + CVFc 15, 15, 19, 29, 32
B6AF1 DBA/2 untreated 13, 14, 15, 20
B6AF1 DBA/2 DSTa 13, 13, 14, 15, 15
B6AF1 DBA/2 DSTa + MR1b 20, 24, 24, 40, >120
B6AF1 Balb/c untreated 9, 11, 13, 15, 17
B6AF1 Balb/c DSTa 7, 7, 8, 9, 10, 12
B6AF1 Balb/c DSTa + MR1b >60, >60, >60, >60
129 CD40KO Balb/c CD40KO untreated 9, 12, 13, 17
129 CD40KO Balb/c CD40KO DSTa 6, 6, 7, 9, 10
129 CD40KO Balb/c CD40KO DSTa + MR1b 8, 19, 22, >120, >120, >120
a

DST consisted of 0.25 mL fresh donor whole blood administered 28 days before transplantation.

b

MR1 anti-CD154 mAb was given at a single dose of 0.5 mg/mouse intravenously 28 days before transplantation.

c

CVF was given at a dose of 60 units/kg intraperitoneally 28 days before transplantation followed by 20 units/kg per day for 14 consecutive days.

DST, donor specific transfusion; CVF, cobra venom factor.