A digital single-molecule nanopillar SERS platform for predicting and monitoring immune toxicities in immunotherapy.
Junrong LiAlain WuethrichAbu Ali Ibn SinaHan-Hao ChengYuling WangAndreas BehrenPaul N MainwaringMatt TrauPublished in: Nature communications (2021)
The introduction of immune checkpoint inhibitors has demonstrated significant improvements in survival for subsets of cancer patients. However, they carry significant and sometimes life-threatening toxicities. Prompt prediction and monitoring of immune toxicities have the potential to maximise the benefits of immune checkpoint therapy. Herein, we develop a digital nanopillar SERS platform that achieves real-time single cytokine counting and enables dynamic tracking of immune toxicities in cancer patients receiving immune checkpoint inhibitor treatment - broader applications are anticipated in other disease indications. By analysing four prospective cytokine biomarkers that initiate inflammatory responses, the digital nanopillar SERS assay achieves both highly specific and highly sensitive cytokine detection down to attomolar level. Significantly, we report the capability of the assay to longitudinally monitor 10 melanoma patients during immune inhibitor blockade treatment. Here, we show that elevated cytokine concentrations predict for higher risk of developing severe immune toxicities in our pilot cohort of patients.
Keyphrases
- end stage renal disease
- single molecule
- high throughput
- gold nanoparticles
- chronic kidney disease
- ejection fraction
- sensitive detection
- prognostic factors
- label free
- squamous cell carcinoma
- randomized controlled trial
- clinical trial
- study protocol
- raman spectroscopy
- stem cells
- patient reported outcomes
- climate change
- mass spectrometry
- mesenchymal stem cells
- quantum dots
- loop mediated isothermal amplification