Super-resolution microscopy reveals ultra-low CD19 expression on myeloma cells that triggers elimination by CD19 CAR-T.
Thomas NerreterSebastian LetschertRalph GötzSören DooseSophia DanhofHermann EinseleMarkus SauerMichael HudecekPublished in: Nature communications (2019)
Immunotherapy with chimeric antigen receptor-engineered T-cells (CAR-T) is under investigation in multiple myeloma. There are reports of myeloma remission after CD19 CAR-T therapy, although CD19 is hardly detectable on myeloma cells by flow cytometry (FC). We apply single molecule-sensitive direct stochastic optical reconstruction microscopy (dSTORM), and demonstrate CD19 expression on a fraction of myeloma cells (10.3-80%) in 10 out of 14 patients (density: 13-5,000 molecules per cell). In contrast, FC detects CD19 in only 2 of these 10 patients, on a smaller fraction of cells. Treatment with CD19 CAR-T in vitro results in elimination of CD19-positive myeloma cells, including those with <100 CD19 molecules per cell. Similar data are obtained by dSTORM analyses of CD20 expression on myeloma cells and CD20 CAR-T. These data establish a sensitivity threshold for CAR-T and illustrate how super-resolution microscopy can guide patient selection in immunotherapy to exploit ultra-low density antigens.
Keyphrases
- induced apoptosis
- multiple myeloma
- single molecule
- newly diagnosed
- cell cycle arrest
- high resolution
- nk cells
- poor prognosis
- endoplasmic reticulum stress
- ejection fraction
- flow cytometry
- high speed
- immune response
- machine learning
- cell death
- rheumatoid arthritis
- binding protein
- atomic force microscopy
- big data
- long non coding rna
- smoking cessation
- dendritic cells
- cell therapy
- prognostic factors
- drug induced
- living cells
- mass spectrometry
- disease activity