[1][2] Typically, one of the Fabs binds to a tumour antigen (such as CD30) and the other to a protein on the surface of an immune cell, for example an Fc receptor on a macrophage.
[3] In the late 1990s and early 2000s, clinical trials with chemically linked Fabs were conducted for the treatment of various types of cancer.
Early results were promising,[3][4] but the concept was dropped because of high production costs.
[5] Bi-specific T-cell engagers employ a similar mechanism of action while being cheaper.
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