MISSTE: a multiscale integrative spatial simulator for understanding the mechanisms underlying tissue ecosystems
Su, Z.; Yin, S.; Wu, Y.
Show abstract
Multiscale tissue ecosystems are governed by coupled intracellular decision-making, cell-cell interactions, and spatially structured microenvironmental signals, yet these scales are often studied separately. Here we present MISSTE, a modular framework that integrates Boolean intracellular state logic, agent-based modeling, and partial differential equation fields within a unified spatial simulation architecture. As a proof of concept, we applied MISSTE to CAR-T therapy in a solid tumor microenvironment. The model recapitulated emergent features of CAR-T behavior, including limited tumor penetration, stromal suppression, localized cytokine remodeling, hypoxia-associated constraint, and progressive functional exhaustion. Comparison of baseline and optimized conditions showed that coordinated enhancement of interaction range, migration, and cytotoxic function improved immune persistence and partial tumor control. Systematic parameter scans further identified effective immune-tumor contact as a stronger determinant of outcome than killing strength alone, highlighting spatial access as the dominant bottleneck. Guided by these results, we designed sequential intervention strategies and found that time-ordered enhancement of infiltration, killing, and late functional protection outperformed a static optimized regime. Together, these results establish MISSTE as a generalizable multiscale methodology for dissecting tissue ecosystems and for generating mechanistically grounded strategies for engineered cellular therapy design.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
- Selection-driven tumor evolution involving non-cell growth promotion leads to patterns of clonal expansion consistent with neutrality interpretation 95%
- The inherent fragility of collective proliferative control 95%
- A persistent invasive phenotype in post-hypoxic tumor cells is revealed by novel fate-mapping and computational modeling 95%
Similar papers in this journal
- Mathematical deconvolution of CAR T-cell proliferation and exhaustion from real-time killing assay data 95%
- A stochastic mathematical model of 4D tumour spheroids with real-time fluorescent cell cycle labelling 95%
- Different responses to cell crowding determine the clonal fitness of p53 and Notch inhibiting mutations in squamous epithelia 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.