Publication

Systematic evaluation of immune regulation and modulation

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Last modified
  • 05/14/2025
Type of Material
Authors
    David F. Stroncek, National Institutes of HealthLisa H. Butterfield, University of PittsburghMichael A. Cannarile, Roche Innovation Center MunichMadhav Dhodapkar, Emory UniversityTim F. Greten, National Cancer InstituteJean Charles Grivel, Sidra Medical and Research CenterDavid R. Kaufman, Merck Research LaboratoriesHeidi H. Kong, National Cancer InstituteFirouzeh Korangy, National Cancer InstitutePeter P. Lee, City Hope National Medical CenterFrancesco Marincola, Sidra Medical and Research CenterSergio Rutella, Nottingham Trent UniversityJanet C. Siebert, CytoAnalyticsGiorgio Trinchieri, National Cancer InstituteBarbara Seliger, Martin Luther University Halle Wittenberg
Language
  • English
Date
  • 2017-03-21
Publisher
  • BMJ Publishing Group: Open Access
Publication Version
Copyright Statement
  • © 2017 The Author(s).
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 2051-1426
Volume
  • 5
Issue
  • 1
Start Page
  • 21
End Page
  • 21
Abstract
  • Cancer immunotherapies are showing promising clinical results in a variety of malignancies. Monitoring the immune as well as the tumor response following these therapies has led to significant advancements in the field. Moreover, the identification and assessment of both predictive and prognostic biomarkers has become a key component to advancing these therapies. Thus, it is critical to develop systematic approaches to monitor the immune response and to interpret the data obtained from these assays. In order to address these issues and make recommendations to the field, the Society for Immunotherapy of Cancer reconvened the Immune Biomarkers Task Force. As a part of this Task Force, Working Group 3 (WG3) consisting of multidisciplinary experts from industry, academia, and government focused on the systematic assessment of immune regulation and modulation. In this review, the tumor microenvironment, microbiome, bone marrow, and adoptively transferred T cells will be used as examples to discuss the type and timing of sample collection. In addition, potential types of measurements, assays, and analyses will be discussed for each sample. Specifically, these recommendations will focus on the unique collection and assay requirements for the analysis of various samples as well as the high-throughput assays to evaluate potential biomarkers.
Author Notes
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, Immunology

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