Abstract IA005: Analysis of site-specific CAR T cell efficacy in LBCL and development of novel engineering strategies

Abstract Large B cell lymphomas (LBCLs) occupy diverse anatomic sites (nodal and extranodal), where physical barriers, cellular ecosystems, and inhibitory factors vary. This prompted us to investigate how CAR T cells behave across these distinct locations. We reviewed data from a locally conducted CD19 CAR T-cell clinical trial and observed differences in response rates by disease presentation, consistent with other clinical reports. To further explore this, we used an immunocompetent mouse model of lymphoma to interrogate CAR T cell engraftment and B cell clearance across multiple anatomic sites. Notably, the liver emerged as a site of both poor tumor clearance and frequent relapse. Ex vivo functional assays revealed impaired activity of CAR T cells retrieved from the liver compared to those from the spleen, supporting the concept of site-specific functional imprinting. Liver-derived CAR T cells also exhibited increased expression of inhibitory receptors, particularly CD39 and TIM-3. To identify strategies for enhancing CAR T cell efficacy at sites associated with relapse, we performed an in vivo CRISPR knockout screen using a transcription factor–targeting library. This approach identified perturbations (including both gene disruption and overexpression) that improved CAR T cell function in both tissue-agnostic and site-specific contexts. These candidates were further characterized in vitro and in vivo. Overall, the challenges faced by CAR T cells in LBCL appear to reflect the unique architecture and composition of the tissues in which tumour deposits reside. These findings highlight the importance of understanding site-specific mechanisms of resistance and designing next-generation CAR T cells tailored to overcome them. Citation Format: Gillian Savage, Zachary Morse, Pauline Loos, Kevin Bronischewski, Sherry Tan, Angela Wan, Kevin Hay, Natasha Kekre, Laura Evgin. Analysis of site-specific CAR T cell efficacy in LBCL and development of novel engineering strategies [abstract]. In: Proceedings of the Fifth AACR International Meeting on Advances in Malignant Lymphoma: From Discovery to Clinical Impact; 2026 Jun 24-27; Philadelphia, PA. Philadelphia (PA): AACR; Blood Cancer Discov 2026;7(3_Suppl):Abstract nr IA005.

Authors

Institutions

Publication Details

Journal
Blood Cancer Discovery
Published
2026-06-24
DOI
https://doi.org/10.1158/2643-3249.lymphoma26-ia005
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract IA005: Analysis of site-specific CAR T cell efficacy in LBCL and development of novel engineering strategies

Laura Evgin, Gillian Savage, Pauline Loos, Kevin Bronischewski et al.
Blood Cancer Discovery
CAR-T cell therapy research
article

Abstract IA005: Analysis of site-specific CAR T cell efficacy in LBCL and development of novel engineering strategies

Laura Evgin, Gillian Savage, Pauline Loos, Kevin Bronischewski, Sherry Tan, Natasha Kekre, Angela Wan, Zachary Morse, Kevin Hay
article en

Abstract

Abstract Large B cell lymphomas (LBCLs) occupy diverse anatomic sites (nodal and extranodal), where physical barriers, cellular ecosystems, and inhibitory factors vary. This prompted us to investigate how CAR T cells behave across these distinct locations. We reviewed data from a locally conducted CD19 CAR T-cell clinical trial and observed differences in response rates by disease presentation, consistent with other clinical reports. To further explore this, we used an immunocompetent mouse model of lymphoma to interrogate CAR T cell engraftment and B cell clearance across multiple anatomic sites. Notably, the liver emerged as a site of both poor tumor clearance and frequent relapse. Ex vivo functional assays revealed impaired activity of CAR T cells retrieved from the liver compared to those from the spleen, supporting the concept of site-specific functional imprinting. Liver-derived CAR T cells also exhibited increased expression of inhibitory receptors, particularly CD39 and TIM-3. To identify strategies for enhancing CAR T cell efficacy at sites associated with relapse, we performed an in vivo CRISPR knockout screen using a transcription factor–targeting library. This approach identified perturbations (including both gene disruption and overexpression) that improved CAR T cell function in both tissue-agnostic and site-specific contexts. These candidates were further characterized in vitro and in vivo. Overall, the challenges faced by CAR T cells in LBCL appear to reflect the unique architecture and composition of the tissues in which tumour deposits reside. These findings highlight the importance of understanding site-specific mechanisms of resistance and designing next-generation CAR T cells tailored to overcome them. Citation Format: Gillian Savage, Zachary Morse, Pauline Loos, Kevin Bronischewski, Sherry Tan, Angela Wan, Kevin Hay, Natasha Kekre, Laura Evgin. Analysis of site-specific CAR T cell efficacy in LBCL and development of novel engineering strategies [abstract]. In: Proceedings of the Fifth AACR International Meeting on Advances in Malignant Lymphoma: From Discovery to Clinical Impact; 2026 Jun 24-27; Philadelphia, PA. Philadelphia (PA): AACR; Blood Cancer Discov 2026;7(3_Suppl):Abstract nr IA005.

Blood Cancer DiscoveryVol. 7(3_Supplement)
University of British Columbia (CA), University of Calgary (CA), Ottawa Hospital (CA), Spinal Cord Injury BC (CA), Institute of Cancer Research (CA)
Openalex Percentile: Top 8%
CAR-T cell therapy research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.