| Target disease | Animal model | Dose and routes | Outocomes | References |
| Liver: | | | | | Septic fulminant hepatitis | LPS + GalN (mouse) | rh-HGF 3 mg/kg/d, ip | Inhibition of hepatic failure, anti-apoptosis, improved survival | Kosai et al. [40] | Septic fulminant hepatitis | LPS + GalN (rat) | Adeno-HGF, ip | Improved survival, anti-apoptosis, hepatoprotection | Nomi et al. [64] | Septic hepatitis | LPS (mouse) | rh-HGF 1 mg/kg, sc | Anti-apoptosis, HO-1 induction, IL-10 upregulation, IL-6 downregulation | Kamimoto et al. [28] | Septic hepatitis | LPS (rat) | HGF-producing cell implantation | Anti-coagulation, hepatoprotection | Seto et al. [44] | Kaido et al. [65] | Septic hepatitis | LPS (rat) | rh-HGF 1 mg/kg, iv | Hepatocyte replication | Gao et al. [66] | Septic hepatitis | CPL (rat) | rh-HGF 1 mg/kg, iv | Improved survival, anti-coagulation, hepatoprotection | Kondo et al. [45] |
| Kidney: | | | | | Septic ARF | LPS (mouse) | rh-HGF 1 mg/kg, sc | Improved survival, inhibition of ARF, reduced tubular injury, HO-1 induction | Kamimoto et al. [29] | Albuminuria | LPS (mouse) | rh-HGF 1 mg/kg, sc | Anti-inflammation, reduced albuminuria, nephrin preservation, podocyte protection | Kato et al. [56] |
| Lung: | | | | | Septic ARDS | LPS (mouse) | rh-HGF 1 mg/kg, sc | Suppressed edema, reduced neutrophils, alveoloprotection, HO-1 induction | Kamimoto et al. [29] | Acute lung injury | LPS (mouse) | rh-HGF 1 mg/kg, iv | Enhancement of alveolar cell replication | Gao et al. [66] |
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