Dual Targeting with CAR T Cells to Limit Antigen Escape in Multiple Myeloma.
Sylvain SimonStanley R RiddellPublished in: Blood cancer discovery (2020)
Adoptive T-cell therapy targeting a single tumor antigen can induce remissions of hematologic cancers but relapses often occur due to the outgrowth of tumor cells with absent or low expression of the antigen. Strategies to simultaneousy target multiple antigens are needed to fully capitalize on the promise of this therapeutic strategy. In this issue of Blood Cancer Discovery, Fernández de Larrea and colleagues demonstrate in preclinical models of multiple myeloma that targeting BCMA and GPRC5D simultaneously with T cells engineered to express chimeric antigen receptors specific for these antigens may prevent tumor cell escape. See related article by Fernández de Larrea et al., p. 146.
Keyphrases
- cell therapy
- multiple myeloma
- stem cells
- mesenchymal stem cells
- cancer therapy
- induced apoptosis
- poor prognosis
- dendritic cells
- small molecule
- oxidative stress
- high throughput
- machine learning
- cell cycle arrest
- papillary thyroid
- bone marrow
- squamous cell
- binding protein
- cell proliferation
- young adults
- artificial intelligence