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- W3197349944 abstract "To replace one-size-fits-all cancer immunotherapy with personalized treatment, biomarkers of response and resistance as well as assays to evaluate them in each patient are essential. Among likely determinants of response, the spatial locations and activation states of the immune infiltrate appear critical. Current clinical methods for tissue analysis such as immunohistochemistry are poorly matched to the heterogeneity of the tumor immune microenvironment (TIME). However, multiple tools for analysis of the TIME can now image panels of biomarkers in a single experiment, permit deep profiling to measure dozens of immune features in each sample, and/or facilitate unbiased multiomic analysis at high spatial resolution. Several assays are commercialized with some nearing clinical adoption. In this chapter, we present a broad overview of established and emerging technologies that enable multiplexed detection and spatial mapping of cellular and molecular features of the TIME, highlighting advantages and disadvantages as well as opportunities for future development." @default.
- W3197349944 created "2021-09-13" @default.
- W3197349944 creator A5023858424 @default.
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- W3197349944 creator A5052713451 @default.
- W3197349944 creator A5055403488 @default.
- W3197349944 creator A5067953612 @default.
- W3197349944 date "2022-01-01" @default.
- W3197349944 modified "2023-09-23" @default.
- W3197349944 title "Spatial mapping of the tumor immune microenvironment" @default.
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