Abstract 3508: Breaking down solid tumor barriers with a bispecific T cell engager against a novel pHLA target

Abstract Recent clinical results show the ability to target intracellular proteins through peptides presented by human leukocyte antigen (pHLA), opening up a unique avenue to targets inaccessible to conventional biologics. Bispecific T cell engagers are an effective therapeutic modality to redirect T cell immune responses towards tumors. However, there is still significant unmet need in a number of solid tumor indications with limited treatment options and few pHLA targets. Using a high-throughput discovery platform utilizing experimental screening and machine learning approaches to map patient T cell immune responses to their respective pHLA targets, a novel wildtype tumor-associated pHLA target with sufficient tumor versus normal expression has been identified. This target contributes directly to tumor stability and growth and is widely expressed in colorectal cancer, triple-negative breast cancer, and squamous non-small cell lung cancer among other indications. 3T-403, a CD3 bispecific T cell engager utilizing a T cell receptor mimic (TCRm) antibody has been developed to this novel target. The pHLA binding arm of 3T-403 has undergone specificity analysis using classical alanine scan as well as analysis via a novel high-throughput combinatorial library to de-risk potential pHLA off-targets. Potency assays conducted with 3T-403 show lysis against a panel of tumor cell lines, while minimal cytotoxicity was observed on primary healthy tissues, which provides a therapeutic window. Investigational new drug (IND) application completion is expected early 2026. Such a bispecific T cell engager against a novel target shows significant promise to address multiple solid tumor indications. Citation Format: Marvin H. Gee, Joshua Goldsmith, Ryan Stafford, Christine Cheng, Bindu Hegde, Tina Giese, Tamson Moore, Lisa Kirkemo, Tanmayee Khadilkar, Lena Flood, Jake Kleiner, Florian Schustek, Aurelien Sarde, Joanna Dreux, Alaina K. Cagalingan, Ricardo Herrada, Gabriel Michaels, Kyle Pelot, Azita Tabrizi, Stefan Scherer. Breaking down solid tumor barriers with a bispecific T cell engager against a novel pHLA target [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 3508.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-3508
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 3508: Breaking down solid tumor barriers with a bispecific T cell engager against a novel pHLA target

Tina Giese, Joanna Dreux, Joshua Goldsmith, Marvin H. Gee et al.
Cancer Research
Monoclonal and Polyclonal Antibodies Research
article

Abstract 3508: Breaking down solid tumor barriers with a bispecific T cell engager against a novel pHLA target

Tina Giese, Joanna Dreux, Joshua Goldsmith, Marvin H. Gee, Kyle Pelot, Lisa L. Kirkemo, Bindu Hegde, Ryan Stafford, Lena Flood, Azita Tabrizi, Jake Kleiner, Tamson V. Moore, Stefan Scherer, Aurélien Sarde, Alaina Cagalingan, Florian Schustek, Christine Cheng, Ricardo Herrada, Gabriel Michaels, Tanmayee Khadilkar
article en

Abstract

Abstract Recent clinical results show the ability to target intracellular proteins through peptides presented by human leukocyte antigen (pHLA), opening up a unique avenue to targets inaccessible to conventional biologics. Bispecific T cell engagers are an effective therapeutic modality to redirect T cell immune responses towards tumors. However, there is still significant unmet need in a number of solid tumor indications with limited treatment options and few pHLA targets. Using a high-throughput discovery platform utilizing experimental screening and machine learning approaches to map patient T cell immune responses to their respective pHLA targets, a novel wildtype tumor-associated pHLA target with sufficient tumor versus normal expression has been identified. This target contributes directly to tumor stability and growth and is widely expressed in colorectal cancer, triple-negative breast cancer, and squamous non-small cell lung cancer among other indications. 3T-403, a CD3 bispecific T cell engager utilizing a T cell receptor mimic (TCRm) antibody has been developed to this novel target. The pHLA binding arm of 3T-403 has undergone specificity analysis using classical alanine scan as well as analysis via a novel high-throughput combinatorial library to de-risk potential pHLA off-targets. Potency assays conducted with 3T-403 show lysis against a panel of tumor cell lines, while minimal cytotoxicity was observed on primary healthy tissues, which provides a therapeutic window. Investigational new drug (IND) application completion is expected early 2026. Such a bispecific T cell engager against a novel target shows significant promise to address multiple solid tumor indications. Citation Format: Marvin H. Gee, Joshua Goldsmith, Ryan Stafford, Christine Cheng, Bindu Hegde, Tina Giese, Tamson Moore, Lisa Kirkemo, Tanmayee Khadilkar, Lena Flood, Jake Kleiner, Florian Schustek, Aurelien Sarde, Joanna Dreux, Alaina K. Cagalingan, Ricardo Herrada, Gabriel Michaels, Kyle Pelot, Azita Tabrizi, Stefan Scherer. Breaking down solid tumor barriers with a bispecific T cell engager against a novel pHLA target [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 3508.

Cancer ResearchVol. 85(8_Supplement_1)
Wave 80 Biosciences (United States) (US), Catalyst Biosciences (United States) (US)
Openalex Percentile: Top 88%
Monoclonal and Polyclonal Antibodies 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.