Abstract 139: Functional profiling of an allogeneic NK cell therapy product in NSCLC patient-derived organotypic tumor spheroids.

Abstract Allogeneic natural killer (NK) cell therapies offer an off-the-shelf strategy for targeting solid tumors, but their functional activity within complex human tumor microenvironments remains poorly defined. We evaluated an allogeneic NK-cell therapy product design (NK cells) and tested its performance using the Xsphera platform, which incorporates patient-derived organotypic tumor spheroids (PDOTS) embedded in extracellular matrix (ECM) and cultured in microfluidic devices that preserve tumor-immune-stromal architecture ex vivo. Assay conditions were first optimized using LS1034 tumor cell spheroids as target cells and cryopreserved NK cells to identify parameters that maximized NK cell activity, including ECM concentration, effector-to-target (E:T) ratio, exposure duration, and media composition. Under optimal conditions, NK cells induced up to 40% tumor spheroid killing, as quantified by live/dead imaging using Hoechst and propidium iodide staining. We next applied these conditions to PDOTS generated from five non-small cell lung cancer (NSCLC) patients. NK cells were introduced at an estimated 2:1 E:T ratio and cultured for 96 hours. Live/dead imaging revealed significant cytotoxic responses in 2 of 5 PDOTS, with live tumor area reductions of up to 50%. The NK cells expressed activation markers (NKG2D, CD69) and secreted elevated levels of interferon-γ, tumor necrosis factor, and granzyme B. Transcriptomic profiling of the media revealed enrichment of interferon-stimulated genes and cytotoxic effectors. Notably, these molecular features did not correlate with tumor responsiveness. These findings demonstrate the utility of the PDOTS platform for functionally profiling NK cell potency in physiologically relevant tumor models and support its use in the rational development of next-generation NK cell therapy products for solid tumors. Citation Format: Chunxiao Cui, Anthony Attardo, Mei Rosa Ng, Yana Wang, Michael A. Perricone. Functional profiling of an allogeneic NK cell therapy product in NSCLC patient-derived organotypic tumor spheroids [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 139.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-139
Primary Topic
Immune Cell Function and Interaction
Type
article
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article

Abstract 139: Functional profiling of an allogeneic NK cell therapy product in NSCLC patient-derived organotypic tumor spheroids.

Chunxiao Cui, Michael A. Perricone, Mei Rosa Ng, Anthony Attardo et al.
Cancer Research
Immune Cell Function and Interaction
article

Abstract 139: Functional profiling of an allogeneic NK cell therapy product in NSCLC patient-derived organotypic tumor spheroids.

Chunxiao Cui, Michael A. Perricone, Mei Rosa Ng, Anthony Attardo, Yana Wang
article en

Abstract

Abstract Allogeneic natural killer (NK) cell therapies offer an off-the-shelf strategy for targeting solid tumors, but their functional activity within complex human tumor microenvironments remains poorly defined. We evaluated an allogeneic NK-cell therapy product design (NK cells) and tested its performance using the Xsphera platform, which incorporates patient-derived organotypic tumor spheroids (PDOTS) embedded in extracellular matrix (ECM) and cultured in microfluidic devices that preserve tumor-immune-stromal architecture ex vivo. Assay conditions were first optimized using LS1034 tumor cell spheroids as target cells and cryopreserved NK cells to identify parameters that maximized NK cell activity, including ECM concentration, effector-to-target (E:T) ratio, exposure duration, and media composition. Under optimal conditions, NK cells induced up to 40% tumor spheroid killing, as quantified by live/dead imaging using Hoechst and propidium iodide staining. We next applied these conditions to PDOTS generated from five non-small cell lung cancer (NSCLC) patients. NK cells were introduced at an estimated 2:1 E:T ratio and cultured for 96 hours. Live/dead imaging revealed significant cytotoxic responses in 2 of 5 PDOTS, with live tumor area reductions of up to 50%. The NK cells expressed activation markers (NKG2D, CD69) and secreted elevated levels of interferon-γ, tumor necrosis factor, and granzyme B. Transcriptomic profiling of the media revealed enrichment of interferon-stimulated genes and cytotoxic effectors. Notably, these molecular features did not correlate with tumor responsiveness. These findings demonstrate the utility of the PDOTS platform for functionally profiling NK cell potency in physiologically relevant tumor models and support its use in the rational development of next-generation NK cell therapy products for solid tumors. Citation Format: Chunxiao Cui, Anthony Attardo, Mei Rosa Ng, Yana Wang, Michael A. Perricone. Functional profiling of an allogeneic NK cell therapy product in NSCLC patient-derived organotypic tumor spheroids [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 139.

Cancer ResearchVol. 86(7_Supplement)
Coherus BioSciences (United States) (US), Vedantra Pharmaceuticals (United States) (US)
Openalex Percentile: Top 7%
Immune Cell Function and Interaction
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