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In contrast, in situ cancer vaccines leverage the entire tumor antigen repertoire from the outset, enabling rapid, broad, and dynamically expanding polyclonal T-cell responses, whereas personalized vaccines deliver delayed but precisely targeted responses against selected neoantigens

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falciparum growth in the presence of Albumax, we propose that bioavailability cannot solely explain the protective effect of Albumax

by impedance measurement), expressed as cell index

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