Spatial tissue analysis of secondary sarcoma following CAR T cell therapy for B cell lymphoma

CD19-directed chimeric antigen receptor (CAR)-engineered T cells have transformed cellular therapy for hematologic malignancies but have also raised concerns about secondary malignancies. A spatial profiling method was used to analyze the tumor microenvironment and define native and CAR T cell association with a pleomorphic sarcoma arising 12 months post-CAR T therapy for B cell lymphoma. Although CAR T sequences were absent in the secondary tumor, our approach enabled profiling of the stroma, tumor, and infiltrating T cells. Spatial analysis incorporated proteomics via serial antibody staining and transcriptomics using RNA hybridization on an automated MACSima imaging cyclic staining (MICS) system, which allows for in situ detection of CAR T cells. We report here the prevalence of CAR-positive T cells in patient-derived tissue sections, observed metabolic and proliferative shifts in the tumor and its microenvironment, and immune checkpoint analysis. These findings provide insights into post-CAR T secondary cancers and highlight tools that may guide future targeted therapies.

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Publication Details

Journal
iScience
Published
2026-07-17
DOI
https://doi.org/10.1016/j.isci.2026.116847
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

Spatial tissue analysis of secondary sarcoma following CAR T cell therapy for B cell lymphoma

Rimas J. Orentas, Robert Pinard, Jia‐Jye Lee, Dongju Park et al.
iScience
CAR-T cell therapy research
article

Spatial tissue analysis of secondary sarcoma following CAR T cell therapy for B cell lymphoma

Rimas J. Orentas, Robert Pinard, Jia‐Jye Lee, Dongju Park, Yi-Xiang Wang, Lynn O’Donnell, Nathan Denlinger, Kun Luo, Ashley Krull, Sumithira Vasu, Marcos de Lima, Dina Schneider, Peirong Hu, Evandro Bezerra, Pradyot Dash, Lapo Alinari, Wing Keung Chan, Emily Neil, Yazeed Sawalha, Dan Jones
article en

Abstract

CD19-directed chimeric antigen receptor (CAR)-engineered T cells have transformed cellular therapy for hematologic malignancies but have also raised concerns about secondary malignancies. A spatial profiling method was used to analyze the tumor microenvironment and define native and CAR T cell association with a pleomorphic sarcoma arising 12 months post-CAR T therapy for B cell lymphoma. Although CAR T sequences were absent in the secondary tumor, our approach enabled profiling of the stroma, tumor, and infiltrating T cells. Spatial analysis incorporated proteomics via serial antibody staining and transcriptomics using RNA hybridization on an automated MACSima imaging cyclic staining (MICS) system, which allows for in situ detection of CAR T cells. We report here the prevalence of CAR-positive T cells in patient-derived tissue sections, observed metabolic and proliferative shifts in the tumor and its microenvironment, and immune checkpoint analysis. These findings provide insights into post-CAR T secondary cancers and highlight tools that may guide future targeted therapies.

iScienceVol. 29(8)
Miltenyi Biotec (Germany) (DE), Lentigen Technology (United States) (US), The Ohio State University (US)
Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, Miltenyi Biotec
Zero hunger
Openalex Percentile: Top 11%
CAR-T cell therapy research
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