본문으로 건너뛰기
← 뒤로

FOXM1-specific TCR-engineered T cells target non-small cell lung cancer.

1/5 보강
Cancer immunology research 📖 저널 OA 50% 2024: 2/4 OA 2025: 10/22 OA 2026: 22/42 OA 2024~2026 2026
Retraction 확인
출처

Bontekoe E, Zhang M, Jiang P, Montoya A, Shulga Y, Slone JK

📝 환자 설명용 한 줄

FOXM1 is highly expressed in various cancer types and considered a key driver of cancer progression.

이 논문을 인용하기

↓ .bib ↓ .ris
APA Bontekoe E, Zhang M, et al. (2026). FOXM1-specific TCR-engineered T cells target non-small cell lung cancer.. Cancer immunology research. https://doi.org/10.1158/2326-6066.CIR-25-0605
MLA Bontekoe E, et al.. "FOXM1-specific TCR-engineered T cells target non-small cell lung cancer.." Cancer immunology research, 2026.
PMID 41854516 ↗

Abstract

FOXM1 is highly expressed in various cancer types and considered a key driver of cancer progression. Accordingly, we evaluated the immunogenicity of FOXM1 and investigated the feasibility of targeting this transcription factor using T cell receptor (TCR) engineering. We identified epitopes derived from FOXM1 which were immunogenic on HLA-A*02:01, HLA-A*24:02, and HLA-A*23:01, endogenously-processed and presented, and resulted in T cell activation and cytotoxic T cell responses. Following the generation of TCR-T cells, sensitivity and specificity were confirmed by peptide dose-response and X-scan, respectively. Most importantly, adoptive transfer of TCR engineered T cells led to a significant reduction in tumor growth, as well as significantly prolonged survival in a tumor-bearing immunocompromised murine model. Our studies confirm the immunogenicity of FOXM1 and feasibility of targeting this antigen using TCR-engineering.