Mass Spectrometry-Based Multi-Protein Panel Assay for Detecting Immune Checkpoint Proteins in Immune Cells of Oral Cancer Patients

免疫系统 免疫疗法 癌症 癌症免疫疗法 免疫检查点 医学 肿瘤科 癌症研究 临床试验 抗体 不利影响 计算生物学 免疫学 癌细胞 精密医学 个性化医疗 癌症生物标志物 抗原 蛋白质组学 癌症治疗 药品 生物标志物 生物信息学
作者
Anjana Aravind,Chinmaya Narayana Kotimoole,Shubham Sukerndeo Upadhyay,Manavalan Vijayakumar,Rohan Thomas Mathew,Jalaludhin Akbar Kandel Codi,Rohan Shetty,Thottethodi Subrahmanya Keshava Prasad
出处
期刊:Journal of Proteome Research [American Chemical Society]
卷期号:25 (3): 1339-1352
标识
DOI:10.1021/acs.jproteome.5c00664
摘要

Cancer immunotherapy represents a transformative approach to cancer treatment, paving the way for personalized and precision medicine strategies. Despite the significant advances in immunotherapy, the treatment response rate remains a major clinical challenge. The stratification of patients into responders and nonresponders is paramount for immunotherapy treatment response, which reduces the likelihood of treatment challenges, expenses, and potentially severe adverse effects in cases where patients are not likely to respond. Therefore, in the present study, we optimized a mass spectrometry-based analytical assay deploying data-independent acquisition analysis (DIA) to simultaneously detect a panel of six well-known immune checkpoint proteins. Further, the optimized assay was analytically validated to assess the technical performance, and preliminary clinical feasibility testing was conducted using the clinical samples of immune cells from oral cancer patients. Altogether, we tested the method for the detection of the candidate proteins in samples from 20 oral cancer patients and healthy individuals. A proof-of-concept method using DIA-MS was optimized with a shorter turnaround time, facilitating a multiplexed detection and quantitation of protein targets within the panel. This DIA-MS method could be applied to detect potential immune checkpoint proteins without additional enrichment techniques. Furthermore, this optimized method can be used in clinical settings to guide appropriate drug selection based on the abundance of target protein(s) in each patient. The assay may also be adapted for other cancer types using the same multiprotein panel, or expanded in the future to include additional proteins validated as potential immunotherapeutic targets.
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