AUTHOR=Pepple Ashley L. , Guy Joey L. , McGinnis Reliza , Felsted Amy E. , Song Brian , Hubbard Ryan , Worlikar Tejaswi , Garavaglia Hannah , Dib Joe , Chao Hannah , Boyle Nicoleen , Olszewski Michal , Xu Zhen , Ganguly Anutosh , Cho Clifford S. TITLE=Spatiotemporal local and abscopal cell death and immune responses to histotripsy focused ultrasound tumor ablation JOURNAL=Frontiers in Immunology VOLUME=14 YEAR=2023 URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1012799 DOI=10.3389/fimmu.2023.1012799 ISSN=1664-3224 ABSTRACT=Introduction

Histotripsy is a novel focused ultrasound tumor ablation modality with potent immunostimulatory effects.

Methods

To measure the spatiotemporal kinetics of local andabscopal responses to histotripsy, C57BL/6 mice bearing bilateral flank B16 melanoma or Hepa1-6 hepatocellular carcinoma tumors were treated with unilateral sham or partial histotripsy. Treated and contralateral untreated (abscopal) tumors were analyzed using multicolor immunofluorescence, digital spatial profiling, RNA sequencing (RNASeq), and flow cytometry.

Results

Unilateral histotripsy triggered abscopal tumor growth inhibition. Within the ablation zone, early high mobility group box protein 1 (HMGB1) release and necroptosis were accompanied by immunogenic cell death transcriptional responses in tumor cells and innate immune activation transcriptional responses in infiltrating myeloid and natural killer (NK) cells. Delayed CD8+ T cell intratumoral infiltration was spatiotemporally aligned with cancer cell features of ferroptosis; this effect was enhanced by CTLA-4 blockade and recapitulated in vitro when tumor-draining lymph node CD8+ T cells were co-cultured with tumor cells. Inoculation with cell-free tumor fractions generated by histotripsy but not radiation or freeze/thaw conferred partial protection from tumor challenge.

Discussion

We propose that histotripsy may evoke local necroptotic immunogenic cell death, priming systemic adaptive immune responses and abscopal ferroptotic cancer cell death.