CAR T Cell Membrane Camouflaged Nanocatalyst Augments CAR T Cell Therapy Efficacy Against Solid Tumor.
Wenjing WuHaimei LiWenqi ChenYulin HuZichen WangWenyan SheLiang HuangYi LiuPeng JiangPublished in: Small (Weinheim an der Bergstrasse, Germany) (2024)
The immunosuppressive tumor microenvironment (TME) reduces the chimeric antigen receptor (CAR) T-cell therapy against solid tumors. Here, a CAR T cell membrane-camouflaged nanocatalyst (ACSP@TCM) is prepared to augment CAR T cell therapy efficacy against solid tumors. ACSP@TCM is prepared by encapsulating core/shell Au/Cu 2- x Se and 3-bromopyruvate with a CAR T cell membrane. It is demonstrated that the CAR T cell membrane camouflaging has much better-targeting effect than the homologous tumors cell membrane camouflaging. ACSP@TCM has an appealing synergistic chemodynamic/photothermal therapy (CDT/PTT) effect that can induce the immunogenic cell death (ICD) of NALM 6 cells. Moreover, 3-bromopyruvate can inhibit the efflux of lactic acid by inhibiting the glycolysis process, regulating the acidity of TME, and providing a more favorable environment for the survival of CAR T cells. In addition, the photoacoustic (PA) imaging and computed tomography (CT) imaging performance can guide the ACSP@TCM-mediated tumor therapy. The results demonstrated that the ACSP@TCM significantly enhanced the CAR T cell therapy efficacy against NALM 6 solid tumor mass, and completely eliminated tumors. This work provides an effective tumor strategy for CAR T cell therapy in solid tumors.
Keyphrases
- cell therapy
- stem cells
- computed tomography
- mesenchymal stem cells
- cell death
- high resolution
- positron emission tomography
- induced apoptosis
- magnetic resonance imaging
- cell cycle arrest
- cancer therapy
- image quality
- dna damage
- contrast enhanced
- oxidative stress
- bone marrow
- mass spectrometry
- fluorescence imaging
- drug delivery
- dna repair
- pet ct
- metal organic framework