Despite the remarkable clinical success of immunotherapy, its efficacy against hepatocellular carcinoma (HCC) remains severely limited, highlighting an urgent need for novel targets and strategies to overcome immune evasion. Here, we aimed to identify key regulators of HCC immunity via unbiased functional screening and develop a targeted therapy to remodel the immunosuppressive tumor microenvironment (TME). We performed an in vivo CRISPR-knockout screen using a 4500-gene sgRNA library in syngeneic HCC mouse models. Single-cell RNA sequencing of human HCC tissues and in vivo macrophage-depletion assays were utilized to dissect cellular populations and validate underlying mechanisms. We identified ribosomal protein S19 (RPS19) as a central mediator of HCC immune evasion, whose deletion in HCC cells mitigates the immunosuppressive TME. Mechanistically, scRNA-seq pinpointed tumor-associated macrophages as the key effector subset, whereby complement C5a receptor 1 (C5aR1) transduces RPS19 signals to trigger macrophage-dependent immune suppression. We further constructed SP94-peptide-modified disulfide-bond-containing nanoparticles (SNPSS) for targeted CRISPR-Cas9 delivery. SNPSS efficiently homes to HCC cells, releases payloads within the glutathione-rich TME, downregulates RPS19, reverses immune suppression, and robustly suppresses HCC progression in vivo. Collectively, the RPS19-C5aR1-macrophage axis fuels HCC immune escape, and SNPSS-based RPS19 gene-editing offers a promising strategy to remodel the TME and boost HCC immunotherapy efficacy.
