Title | Chimeric Antigen Receptor T Cell Therapy Targeting ICAM-1 in Gastric Cancer. |
Publication Type | Journal Article |
Year of Publication | 2020 |
Authors | Jung M, Yang Y, McCloskey JE, Zaman M, Vedvyas Y, Zhang X, Stefanova D, Gray KD, Min IM, Zarnegar R, Choi YYoung, Cheong J-H, Noh SHoon, Rha SYoung, Chung HCheol, Jin MM |
Journal | Mol Ther Oncolytics |
Volume | 18 |
Pagination | 587-601 |
Date Published | 2020 Sep 25 |
ISSN | 2372-7705 |
Abstract | Cancer therapy utilizing adoptive transfer of chimeric antigen receptor (CAR) T cells has demonstrated remarkable clinical outcomes in hematologic malignancies. However, CAR T cell application to solid tumors has had limited success, partly due to the lack of tumor-specific antigens and an immune-suppressive tumor microenvironment. From the tumor tissues of gastric cancer patients, we found that intercellular adhesion molecule 1 (ICAM-1) expression is significantly associated with advanced stage and shorter survival. In this study, we report a proof-of-concept study using ICAM-1-targeting CAR T cells against gastric cancer. The efficacy of ICAM-1 CAR T cells showed a significant correlation with the level of ICAM-1 expression in target cells . In animal models of human gastric cancer, ICAM-1-targeting CAR T cells potently eliminated tumors that developed in the lungs, while their efficacy was more limited against the tumors in the peritoneum. To augment CAR T cell activity against intraperitoneal tumors, combinations with paclitaxel or CAR activation-dependent interleukin (IL)-12 release were explored and found to significantly increase anti-tumor activity and survival benefit. Collectively, ICAM-1-targeting CAR T cells alone or in combination with chemotherapy represent a promising strategy to treat patients with ICAM-1 advanced gastric cancer. |
DOI | 10.1016/j.omto.2020.08.009 |
Alternate Journal | Mol Ther Oncolytics |
PubMed ID | 32995483 |
PubMed Central ID | PMC7501410 |
Grant List | R01 CA217059 / CA / NCI NIH HHS / United States |
Related Institute:
Molecular Imaging Innovations Institute (MI3)