Laponite Lights Calcium Flickers by Reprogramming Lysosomes to Steer Dc Migration for An Effective Antiviral CD8+ T-Cell Response

Immunotherapy using dendritic cell (DC)-based vaccination is an established approach for treating cancer and infectious diseases; however, its efficacy is limited. Therefore, targeting the restricted migratory capacity of the DCs may enhance their therapeutic efficacy. In this study, the effect of laponite (Lap) on DCs, which can be internalized into lysosomes and induce cytoskeletal reorganization via the lysosomal reprogramming-calcium flicker axis, is evaluated, and it is found that Lap dramatically improves the in vivo homing ability of these DCs to lymphoid tissues. In addition, Lap improves antigen cross-presentation by DCs and increases DC-T-cell synapse formation, resulting in enhanced antigen-specific CD8+ T-cell activation. Furthermore, a Lap-modified cocktail (Lap@cytokine cocktail [C-C]) is constructed based on the gold standard, C-C, as an adjuvant for DC vaccines. Lap@C-C-adjuvanted DCs initiated a robust cytotoxic T-cell immune response against hepatitis B infection, resulting in > 99.6% clearance of viral DNA and successful hepatitis B surface antigen seroconversion. These findings highlight the potential value of Lap as a DC vaccine adjuvant that can regulate DC homing, and provide a basis for the development of effective DC vaccines.

Automated summary

This study evaluated the effect of Lap on DCs and found that Lap dramatically improved the homing ability of DCs to lymphoid tissues and enhanced antigen-specific CD8+ T-cell activation. Additionally, a Lap@C-C adjuvant was constructed for DC vaccines, which initiated a robust cytotoxic T-cell immune response against hepatitis B infection. These findings highlight the potential value of Lap as a DC vaccine adjuvant and provide a basis for effective DC vaccine development.