ArticleRSC advances2026
A lectin-directed antibody-recruiting molecule against Tn antigen for cancer immunotherapy.
Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
6 authors.
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Abstract
The Tn antigen, an abnormally glycosylated structure on the cell surface, is a key target for cancer immunotherapy. However, the intrinsically weak immunogenicity of glycans and the resulting complex immune tolerance constitute the primary challenges in the clinical translation of Tn-targeted immunotherapies. Native human macrophage galactose lectin (MGL) exhibits a strong binding preference for Tn antigen. Here, we report a Tn-targeting, bifunctional antibody-like molecule ZZ-MGL comprised of an antibody-recruiting domain and a lectin domain. It was demonstrated that ZZ-MGL can target the Tn antigen with high avidity while potently recruiting circulating IgGs
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Registered trials
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