“…Altered glycosylations in cancer provide potential targets for therapy [ 21 , 61 , 62 ], but despite numerous developed anti-glycan antibodies [ 63 , 64 , 65 , 66 ], most are not compatible with clinical applications. SLe a is a potential therapeutic target in many types of cancers [ 28 , 29 ], including pancreatic and colorectal cancers [ 59 , 67 , 68 ]. Here, we demonstrate a platform for optimizing functional therapeutic antibodies against cancer glycans, exemplified by targeting SLe a .…”