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. 2018 Sep 5;9:1711. doi: 10.3389/fimmu.2018.01711

Table 2.

The potential genes for CRISPR modification.

Name of the modified gene Benefits for xenotransplantation Reference
Human CD59+ Reduction of activation of serum complement on the luminal surface of the vascular endothelium (35)
Human CD55+ Reduction of activation of serum complement on the luminal surface of the vascular endothelium (36)
Human GLA+ Reduction of interaction of Galα(1,3)Gal with antibodies and complement directed against swine Gal antigen (37)
Human H-transferase+ Reduction of Galα1,3-Gal expression (38)
Human CD46+ Reduction of activation of serum complement on the luminal surface of the vascular endothelium (39)
Human GnT-III+ Reduction of antigenicity to natural human antibodies, especially the Galalpha1-3Galbeta1-4GlcNAc-R (40)
Human TRAIL+ Controlling post-hyperacute rejection mechanisms mediated by cellular components of the immune system (41)
Human DAF and MCP+ Supporting the idea of modulating coagulation pathway activation in transgenic pigs (42)
Porcine CTLA4-Ig+ Reduction of T-cell activity (43)
Human thrombomodulin+ Elevation in activated protein C production to control xenogenic coagulation (44)
HLA-E/Human Beta-2-microglobulin+ Protection against xenogeneic human anti-pig natural killer cell cytotoxicity (45)
Human A20+ Protection against apoptotic and inflammatory stimuli (46)
Endo-B-Galactosidase+ Reduction of alphaGal expression (47)
CIITA-DN+ Reduction of human CD4(+) T-cell proliferation reduction of humoral and cellular responses to the pig aortic endothelial cells (pAECs) (48)
Human Fas Ligand+ Reduction of CD8+ CTL-mediated cytotoxicity (49) (50)
Human TNFRI-Fc+ Reduction of activation of porcine endothelial cells (51)
Human heme oxygenase 1+ Increasing the protection of xenografts when exposed to oxidative stresses, especially from ischemia/reperfusion injury, and/or acute rejection mediated by cytokines (52)
Human CD39+ Protection against myocardial injury and ischemia/reperfusion injury (53)
LEA29Y+ Normalize blood glucose levels and inhibition of human–anti-pig rejection (54)