Although γδ‐T‐EVs + free TAAs also showed a trend in the augment of tumor‐specific T cells in the presence of iDCs, its efficacy was significantly lower than γδ‐T‐EVs preloaded with TAAs (γδ‐T‐EVs (TAAs)) (Figure 2b ).
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Tumor vaccine based on extracellular vesicles derived from γδ-T cells exerts dual antitumor activities.
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