Zonghao Liu

h-index16
2papers
800citations

2 Papers

21.8DCJul 31
Rethinking AI Cloud Infrastructure for Agentic Serving Systems with the Aries Experimentation Framework

Leonid Kondrashov, Hongrui Liu, JooYoung Park et al.

Autonomous agents challenge conventional LLM serving by coupling repeated inference with persistent context and sandboxed tool execution. We present Aries, a full-stack experimentation framework that separates task semantics from execution configurations, reconstructs cross-component agent trajectories with correlated system telemetry, and exposes stateful tool execution through a consistent interface across heterogeneous sandbox substrates. We use Aries to conduct reproducible experiments on open agent harnesses and benchmarks. We complement these experiments with production traces from a commercial platform, grounding low-level systems research in observed production behavior. Our results show that (1) token-centric metrics miss non-inference bottlenecks, (2) retaining additional context yields diminishing accuracy benefits while reducing serving capacity, and (3) tool sandboxes alternate between long idle periods and short resource bursts, while current snapshot-based state management makes aggressive suspension costly. A complementary security analysis further highlights the need to reduce the sandbox attack surface. We then discuss the vision for agent-native serving systems designed around trajectory-level metrics, adaptive context management, elastic sandbox resource management, and sandboxes with minimized attack surface.

8.0APJul 4
Computational Oncology of Chemotaxis-Driven Tumour--Immune Spatial Patterning and Stability

Zonghao Liu, Jiguang Yu, Lei Su et al.

Spatial tumour--immune heterogeneity is a key feature of solid-tumour progression, immune infiltration, and immune exclusion. We develop a computational oncology model in which tumour cells, immune effector cells, and a chemokine signal interact through a reaction--diffusion--chemotaxis system on a bounded tissue domain with no-flux boundaries. Chemokine is produced by tumour cells and tumour--immune contact, recruits immune cells, and guides chemotactic migration. After nondimensionalization, we establish positivity, a tumour-density bound, and immune/chemokine mass estimates. We identify the tumour-free equilibrium, derive the immune-control threshold $σ_0>δ$, and reduce coexistence to a scalar equation. Linear stability analysis about coexistence yields a mode-wise dispersion relation in which chemotaxis appears as a wavenumber amplified coupling, producing finite-wavelength instability above a critical sensitivity. A conservative finite-volume scheme with upwind chemotactic flux verifies the thresholds, dominant unstable modes, sensitivity maps, positivity, convergence, and residual consistency.