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. 2020 Aug 27;12(8):423–435. doi: 10.4254/wjh.v12.i8.423

Table 1.

Potential pathways as targets for existing antibodies

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.