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. 2017 Nov 7;2017:2534653. doi: 10.1155/2017/2534653

Table 1.

The longest (median) reported heterotopic cardiac xenograft survival as a function of donor genetics and immune suppression.

Donor Earlier immune suppression Costimulation blockade
CsA/CyP/steroid ATG/CD20/tacrolimus/sirolimus ATG/LoCD2b/CVF/anti-CD154/MMF ATG/anti-CD40, CD20/CVF/MMF
WT 32§ (21 d) [27]
25 (12 d) [28]
n.r. n.r. n.r.
WT;hCRP 99Δ (26 d) [29]
78Δ (35 d) [30]
109#† (20 d) [31]
137#† (96 d) [32]
139 (27 d) [36] n.r.
GTKO n.r. 128 (22 d) [34] 179 (78 d) [37] n.r.
GTKO;hCRP n.r. 52∇† (28 d) [34] 8 (8 d) 236†¶ (71 d) [5] 149 (84 d) [25]
GTKO;hCRP;TBM n.r. n.r. n.r. 945 (298 d) [8]

n.r.: none reported. §Soluble CR1 to block complement activation. Cobra venom factor at 0.25–0.5 mg/kg prior to surgery and 0.1–0.5 mg/kg every 1–4 days thereafter. Included use of alpha-Gal polymer GAS914 [127] or Nex1285 [128]. Immune suppression included anti-CD20 (Rituximab) B-cell depletion. ΔhDAF (human CD55) minigene [129]. A murine H-2Kb regulated human CD55 transgene [77]. #hCD46 transgene based on 60 kb human genomic CD46 DNA [130]. hCD46 transgene based on a human CD46 minigene [131].