In-Vivo experiment designed to assess clinical efficacy targeting N/A in 3xTg-AD mice with stratified p-tau217 status, IV exosome dosing. Primary outcome: Plasma p-tau217 biomarker levels and amyloid/tau pathology burden
Determine the optimal dosing window for p-tau217-triggered hUC-MSC exosome administration delivering lncRNA-0021, based on biomarker stratification, and evaluate neuroprotective efficacy in 3xTg-AD mice.
in-vivo
P-tau217-stratified dosing reduces amyloid and tau pathology by >30% and improves cognitive performance (Y-maze, Barnes maze) vs. standard-dose exosome or vehicle controls.
p-Tau217 plasma levels (ULSA), amyloid/tau IHC burden, cognitive behavioral scores; threshold: p < 0.05 vs. vehicle.
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