Abstract
Immune-based therapies are designed to generate or augment anti-tumor immune responses to achieve clinical benefit. Monitoring quantitative and qualitative parameters of immune function affords the opportunity to identify endpoints that correlate with, or predict clinical benefit and define the requirements for effective therapy. This chapter discusses structural and functional methods to assess both monoclonal and polyclonal antigen-specific T cell responses in vivo in humans. The most adequate methods to detect responses in blood and tumor tissue are examined with a focus on the information provided by evaluating the phenotype of tumor-specific cells. Because considerable variability in the type and performance of immune-monitoring assays exists, harmonization is required to render meaningful comparisons among the increasing number and complexity of immune-based clinical trials.
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Chapuis, A.G., Yee, C. (2013). Monitoring Antigen-Specific Responses in Clinical Trials of Cancer Immunotherapy. In: Curiel, T. (eds) Cancer Immunotherapy. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-4732-0_14
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