Proton radiation boosts the efficacy of mesothelin-targeting chimeric antigen receptor T cell therapy in pancreatic cancer.
Mesothelin
Animals
Pancreatic Neoplasms
/ therapy
Mice
GPI-Linked Proteins
/ metabolism
Receptors, Chimeric Antigen
/ immunology
Immunotherapy, Adoptive
/ methods
Tumor Microenvironment
/ immunology
Humans
Carcinoma, Pancreatic Ductal
/ therapy
Cell Line, Tumor
Proton Therapy
/ methods
Combined Modality Therapy
T-Lymphocytes
/ immunology
Female
CAR T cells
pancreatic cancer
radiotherapy
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876
Informations de publication
Date de publication:
30 Jul 2024
30 Jul 2024
Historique:
medline:
26
7
2024
pubmed:
26
7
2024
entrez:
24
7
2024
Statut:
ppublish
Résumé
Pancreatic ductal adenocarcinoma (PDAC) represents a challenge in oncology, with limited treatment options for advanced-stage patients. Chimeric antigen receptor T cell (CAR T) therapy targeting mesothelin (MSLN) shows promise, but challenges such as the hostile immunosuppressive tumor microenvironment (TME) hinder its efficacy. This study explores the synergistic potential of combining proton radiation therapy (RT) with MSLN-targeting CAR T therapy in a syngeneic PDAC model. Proton RT significantly increased MSLN expression in tumor cells and caused a significant increase in CAR T cell infiltration into tumors. The combination therapy reshaped the immunosuppressive TME, promoting antitumorigenic M1 polarized macrophages and reducing myeloid-derived suppressor cells (MDSC). In a flank PDAC model, the combination therapy demonstrated superior attenuation of tumor growth and improved survival compared to individual treatments alone. In an orthotopic PDAC model treated with image-guided proton RT, tumor growth was significantly reduced in the combination group compared to the RT treatment alone. Further, the combination therapy induced an abscopal effect in a dual-flank tumor model, with increased serum interferon-γ levels and enhanced proliferation of extratumoral CAR T cells. In conclusion, combining proton RT with MSLN-targeting CAR T therapy proves effective in modulating the TME, enhancing CAR T cell trafficking, and exerting systemic antitumor effects. Thus, this combinatorial approach could present a promising strategy for improving outcomes in unresectable PDAC.
Identifiants
pubmed: 39047033
doi: 10.1073/pnas.2403002121
doi:
Substances chimiques
Mesothelin
J27WDC343N
GPI-Linked Proteins
0
Receptors, Chimeric Antigen
0
Msln protein, mouse
0
MSLN protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2403002121Subventions
Organisme : NCI NIH HHS
ID : P30 CA016520
Pays : United States
Organisme : Tel Aviv Medical Center
ID : Postdoctoral training
Organisme : Deutsche Krebshilfe (German Cancer Aid)
ID : Mildred-Scheel Postdoctoroal Fellowship
Déclaration de conflit d'intérêts
Competing interests statement:R.M.Y. and C.H.J. are inventors of patents and/or patent applications licensed to Novartis Institutes of Biomedical Research and receive license revenue from such licenses. C.H.J. is an inventor on patents and/or patent applications licensed to Kite Pharma, Capstan Therapeutics. Dispatch Therapeutics and BlueWhale Bio. C.H.J. is a member of the scientific advisory boards of AC Immune, BluesphereBio, BlueWhale Bio, Cabaletta, Carisma, Cartography, Cellares, Celldex, Decheng, Poseida, Replay Bio, Verismo, ViTToria, and WIRB-Copernicus. No competing interests were declared by U.A., U.U., I.I.V., M.M.K., S.A.O.M., E.S.D., C.-A.A., S.B., S.J.A., E.B.-J., and C.K.