Characterization of an expanded set of assays for immunomodulatory proteins using targeted mass spectrometry.
Jeffrey R WhiteakerLei ZhaoRegine M SchoenherrDongqing HuangJacob J KennedyRichard G IveyChenwei LinTravis D LorentzenSimona ColantonioTessa W CaceresRhonda R RobertsJoseph G KnottsJoshua J ReadingCandice D PerrySandra S Garcia-BuntleyWilliam BocikStephen M HewittAmanda G PaulovichPublished in: Scientific data (2024)
Immunotherapies are revolutionizing cancer care, but many patients do not achieve durable responses and immune-related adverse events are difficult to predict. Quantifying the hundreds of proteins involved in cancer immunity has the potential to provide biomarkers to monitor and predict tumor response. We previously developed robust, multiplexed quantitative assays for immunomodulatory proteins using targeted mass spectrometry, providing measurements that can be performed reproducibly and harmonized across laboratories. Here, we expand upon those efforts in presenting data from a multiplexed immuno-oncology (IO)-3 assay panel targeting 43 peptides representing 39 immune- and inflammation-related proteins. A suite of novel monoclonal antibodies was generated as assay reagents, and the fully characterized antibodies are made available as a resource to the community. The publicly available dataset contains complete characterization of the assay performance, as well as the mass spectrometer parameters and reagent information necessary for implementation of the assay. Quantification of the proteins will provide benefit to correlative studies in clinical trials, identification of new biomarkers, and improve understanding of the immune response in cancer.
Keyphrases
- high throughput
- mass spectrometry
- clinical trial
- immune response
- papillary thyroid
- high resolution
- healthcare
- cancer therapy
- end stage renal disease
- single cell
- primary care
- ejection fraction
- mental health
- newly diagnosed
- oxidative stress
- chronic kidney disease
- liquid chromatography
- high performance liquid chromatography
- randomized controlled trial
- squamous cell carcinoma
- dendritic cells
- risk assessment
- drug delivery
- toll like receptor
- lymph node metastasis
- social media
- machine learning
- young adults
- childhood cancer
- climate change
- patient reported outcomes
- health information
- open label
- phase iii
- drug induced