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Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
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Repurposing vaccine-induced anti-HBV antibodies for endogenous immunotherapy against EGFR-positive tumors
Zijiang Zhang1, Yanchun Li1, Haofei Hong1
1The Key Laboratory of Carbohydrate Chemistry & Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi 214122, China. zwu@jiangnan.edu.cn.
A nanobody chimera composed of an EGFR-targeting nanobody and the LOOP1 peptide derived from HBV surface antigen is capable of harnessing HBV vaccine-induced immunity for cancer immunotherapy.
A nanobody chimera composed of an EGFR-targeting nanobody and the LOOP1 peptide derived from HBV surface antigen is capable of harnessing HBV vaccine-induced immunity for cancer immunotherapy.

