Advancing precision cancer immunotherapy drug development, administration, and response prediction with AI-enabled Raman spectroscopy

被引:2
作者
Chadokiya, Jay [1 ]
Chang, Kai [2 ]
Sharma, Saurabh [1 ]
Hu, Jack [3 ]
Lill, Jennie R. [4 ]
Dionne, Jennifer [3 ,5 ,6 ]
Kirane, Amanda [1 ]
机构
[1] Stanford Univ, Stanford Sch Med, Dept Surg, Med Ctr, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Elect Engn, Stanford, CA USA
[3] Pumpkinseed Technol, Palo Alto, CA 94306 USA
[4] Genentech Inc, South San Francisco, CA USA
[5] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[6] Stanford Univ, Dept Radiol, Mol Imaging Program Stanford MIPS, Sch Med, Stanford, CA 94305 USA
关键词
Raman spectroscopy; label-free analysis; immunotherapy; time analysis; multiomics; SURFACE-ENHANCED RAMAN; PD-L1; EXPRESSION; CELL-DEATH; SPECTRA; BIOMARKERS; PERSPECTIVE; ASSOCIATION; METABOLISM; ACTIVATION; MECHANISMS;
D O I
10.3389/fimmu.2024.1520860
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Molecular characterization of tumors is essential to identify predictive biomarkers that inform treatment decisions and improve precision immunotherapy development and administration. However, challenges such as the heterogeneity of tumors and patient responses, limited efficacy of current biomarkers, and the predominant reliance on single-omics data, have hindered advances in accurately predicting treatment outcomes. Standard therapy generally applies a "one size fits all" approach, which not only provides ineffective or limited responses, but also an increased risk of off-target toxicities and acceleration of resistance mechanisms or adverse effects. As the development of emerging multi- and spatial-omics platforms continues to evolve, an effective tumor assessment platform providing utility in a clinical setting should i) enable high-throughput and robust screening in a variety of biological matrices, ii) provide in-depth information resolved with single to subcellular precision, and iii) improve accessibility in economical point-of-care settings. In this perspective, we explore the application of label-free Raman spectroscopy as a tumor profiling tool for precision immunotherapy. We examine how Raman spectroscopy's non-invasive, label-free approach can deepen our understanding of intricate inter- and intra-cellular interactions within the tumor-immune microenvironment. Furthermore, we discuss the analytical advances in Raman spectroscopy, highlighting its evolution to be utilized as a single "Raman-omics" approach. Lastly, we highlight the translational potential of Raman for its integration in clinical practice for safe and precise patient-centric immunotherapy.
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页数:22
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