High-Intensity thermal stress enhances adoptive NK-cell cytotoxicity in poorly differentiated hepatocellular carcinoma.

Abstract

Background: Percutaneous thermal ablation is used to treat early-stage, non-resectable hepatocellular carcinoma (HCC). NK-cell immunotherapy has been studied as an adjuvant treatment, but the efficacy remains unclear when combined with ablation.

Purpose: To evaluate the potential of peri-ablational, high-intensity thermal stress to augment adoptive NK-cell cytotoxicity in HCC.

Methods: HCC cells were exposed to 37, 43, and 47 °C in water baths to recapitulate peri-ablational heat stress before delivering NK-cell therapy. In vitro cytolysis was measured using chromium release and live-cell imaging assays. An orthotopic mouse model of poorly differentiated HCC was used to evaluate the therapeutic effect of combined microwave ablation (MWA) and adoptive NK-cell therapy. Tumor burden was compared via tumor weight, Gaussia luciferase levels, and immunohistochemistry.

Results: NK-cell cytotoxicity increased against poorly differentiated HCC cells pretreated at 47 °C compared with 37 °C controls (p < 0.001). In vivo, MWA+NK-cell therapy reduced poorly differentiated HCC weight (1.53 ± 0.44 g) compared to monotherapy groups (MWA: 2.06 ± 0.61; NK: 1.92 ± 0.75 g), although the difference was only found to be significant when compared to untreated tumor group (2.89 ± 0.92 g, p < 0.01). Additionally, MWA+NK-cell therapy significantly decreased Gaussia luciferase level (p < 0.05) and Ki-67 expression (p < 0.01), while increasing tumor necrosis (p < 0.05) in tumors when compared to tumor control.

Conclusion: High intensity thermal stress increased susceptibility of poorly differentiated HCC to NK-cell-mediated cytotoxicity in vitro and in vivo when compared to untreated controls. The combination of thermal ablation and adoptive NK-cell therapy should be further investigated in clinically relevant sub-lethal ablation settings and broader ablation-time combinations to support future clinical studies.