Abstract A022: A naturally occurring feline model for human indolent intestinal T-cell neoplasia

Abstract Low grade intestinal T-cell lymphoma (LGITL) is the most common gastrointestinal cancer in cats and is hypothesized to arise from chronic inflammation (lymphoplasmacytic enteritis, LPE), paralleling human refractory celiac disease II (RCD II). RCD II is now classified as an indolent neoplasm characterized by clonal T-cell expansion and JAK/STAT pathway mutations. Fifty percent of RCD II cases will progress to enteropathy-associated T-cell lymphoma, an aggressive disease with a five-year survival of 3-20% with treatment. We propose that feline LPE-LGITL is a naturally occurring translational model for the progression of intestinal inflammation to T-cell neoplasia. To investigate parallels between the human and feline conditions, we performed bulk RNA sequencing on 141 intestinal biopsies (duodenum and ileum) from 71 cats across the LPE-LGITL spectrum. Gene set enrichment analysis revealed that the top upregulated pathways in LGITL included T-cell activation and differentiation, with an enrichment for alpha-beta T-cell and NKT-like/cytotoxic signatures. These findings suggest the tumor cell of origin is an activated, intraepithelial alpha-beta T-cell with NK-like features, similar to the proposed cell of origin in human RCD II. We also identified the activating STAT5BN642H mutation in feline LGITL, and a subset of LPE cases, supporting a stepwise progression from inflammation to neoplasia. Finally, T-cell receptor analysis of LGITL shows multiple unique expanded T-cell clones in a single sample. This suggests LGITL is a cancer with neoplastic cell diversity/heterogeneity, an unusual phenotype that has also been observed in RCD II. Although feline LPE is not driven by gluten, given the similarities in transcriptomic, genetic, and pathological features, we propose that cats offer a valuable preclinical model to study the pathogenesis and treatment of intestinal intraepithelial T-cell lymphomas. Citation Format: Shay Curry, Emily Rout, Adam Harris, Cora Contreras, Robert Burnett, Kelly Hughes, Paula Schaffer, Lauren Harris, Craig Webb, Anne Avery. A naturally occurring feline model for human indolent intestinal T-cell neoplasia [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 A022.

Authors

Institutions

Publication Details

Journal
Blood Cancer Discovery
Published
2026-06-24
DOI
https://doi.org/10.1158/2643-3249.lymphoma26-a022
Primary Topic
Veterinary Oncology Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract A022: A naturally occurring feline model for human indolent intestinal T-cell neoplasia

Adam Harris, Anne Avery, Emily Rout, Kelly Hughes et al.
Blood Cancer Discovery
Veterinary Oncology Research
article

Abstract A022: A naturally occurring feline model for human indolent intestinal T-cell neoplasia

Adam Harris, Anne Avery, Emily Rout, Kelly Hughes, Craig Webb, Robert Burnett, Cora Contreras, Lauren Harris, Paula Schaffer, Shay Curry
article en

Abstract

Abstract Low grade intestinal T-cell lymphoma (LGITL) is the most common gastrointestinal cancer in cats and is hypothesized to arise from chronic inflammation (lymphoplasmacytic enteritis, LPE), paralleling human refractory celiac disease II (RCD II). RCD II is now classified as an indolent neoplasm characterized by clonal T-cell expansion and JAK/STAT pathway mutations. Fifty percent of RCD II cases will progress to enteropathy-associated T-cell lymphoma, an aggressive disease with a five-year survival of 3-20% with treatment. We propose that feline LPE-LGITL is a naturally occurring translational model for the progression of intestinal inflammation to T-cell neoplasia. To investigate parallels between the human and feline conditions, we performed bulk RNA sequencing on 141 intestinal biopsies (duodenum and ileum) from 71 cats across the LPE-LGITL spectrum. Gene set enrichment analysis revealed that the top upregulated pathways in LGITL included T-cell activation and differentiation, with an enrichment for alpha-beta T-cell and NKT-like/cytotoxic signatures. These findings suggest the tumor cell of origin is an activated, intraepithelial alpha-beta T-cell with NK-like features, similar to the proposed cell of origin in human RCD II. We also identified the activating STAT5BN642H mutation in feline LGITL, and a subset of LPE cases, supporting a stepwise progression from inflammation to neoplasia. Finally, T-cell receptor analysis of LGITL shows multiple unique expanded T-cell clones in a single sample. This suggests LGITL is a cancer with neoplastic cell diversity/heterogeneity, an unusual phenotype that has also been observed in RCD II. Although feline LPE is not driven by gluten, given the similarities in transcriptomic, genetic, and pathological features, we propose that cats offer a valuable preclinical model to study the pathogenesis and treatment of intestinal intraepithelial T-cell lymphomas. Citation Format: Shay Curry, Emily Rout, Adam Harris, Cora Contreras, Robert Burnett, Kelly Hughes, Paula Schaffer, Lauren Harris, Craig Webb, Anne Avery. A naturally occurring feline model for human indolent intestinal T-cell neoplasia [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 A022.

Blood Cancer DiscoveryVol. 7(3_Supplement)
Colorado State University (US)
Good health and well-being
Openalex Percentile: Top 7%
Veterinary Oncology 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.