Table 1.
Drug | Primary role of the pathway in specific cholestatic liver disease | Previous disease of drug-testing | Ref. |
Anti-CD40 (dacetuzumab/lucatumumab) | T-cell-B-cell interactions in primary biliary cholangitis | Multiple sclerosis (pre-clinical) | [53] |
Anti-CXCL10 (MDX-1100) | CXCR3-CXCL9/10/11 CXCR3 is upregulated on liver-infiltrating Th1 and Th17 in primary biliargy cholangitis | Rheumatoid arthritis | [54] |
Anti-CXCL13 (Mab 5261) | T- and B-cell migration to germinal centers in primary biliary cholangitis | Preclinical development | [55] |
Anti-CCR6 | Recruitment of Th17 cells around inflamed biliary epithelial cells in primary biliary cholangitis | Preclinical development | [56] |
Anti-GRP35 | Activation of GPR35 reduces IL-4 release from natural killer T cells in primary sclerosing cholangitis | Antibody recently developed | [57] |
Anti-PRKD2 | SIK2 pathway in PSC, AMPK-related kinase PRKD2 polymorphism are seen in early inflammatory bowel disease in primary sclerosing cholangitis | Preclinical development | [58] |
PSC: Primary sclerosing cholangitis.