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Flow Cytometry in Cancer Immunotherapy: Applications, Quality Assurance, and Future

  • Cécile Gouttefangeas
  • Steffen Walter
  • Marij J. P. Welters
  • Christian Ottensmeier
  • Sjoerd H. van der Burg
  • Cedrik M. Britten
  • Cliburn ChanEmail author
Chapter

Abstract

Cancer immunotherapy seeks to elicit or augment the antitumor immune response in a patient in order to enlist the help of the patient’s own immune system for tumor control. In this context, immune monitoring provides evidence of immunogenicity, guides the choice and dosage of antigens, assesses the effects of immune modulators and therapy combinations, and has the potential to reveal early biomarkers of clinical efficacy. In view of their role in the anticancer immune response, the quantity and quality of tumor antigen-specific effector CD4+ and CD8+ T cells are of particular interest, and characterization of regulatory T cells and myeloid-derived suppressor cells is increasingly relevant. The canonical multiparameter assay for the characterization of immune cells is polychromatic flow cytometry, and it is ubiquitously used for immune monitoring in preclinical tumor immunology and in cancer immunotherapy trials. This chapter describes the main flow cytometry methods being applied in cancer immunotherapy, with an emphasis on recent progress in the field, challenges associated with quality control, its promise to reveal biomarkers of clinical efficacy, and further developments that are likely to be rapidly implemented in routine cancer immunology.

Keywords

Cancer Immunotherapy Intracellular Cytokine Staining Immune Monitoring Cancer Immunology Peripheral Blood Mononuclear Cell Sample 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgments

CG, SW, MJP, SvB, CO, and CB are members of the steering committee of the CIMT Immunoguiding Program (CIP). The CIP and CC are supported by a grant of the Wallace Coulter Foundation (Miami, Florida). CG is supported by a grant of the Deutsche Forschungsgemeinschaft SFB685. CC is supported by grants to the Duke University Center for AIDS Research and EQAPOL program funded by NIH grant 5P30 AI064518 and NIH contract HHSN272201000045C, respectively. We thank S Heidu for excellent technical assistance.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2015

Authors and Affiliations

  • Cécile Gouttefangeas
    • 1
  • Steffen Walter
    • 2
  • Marij J. P. Welters
    • 3
  • Christian Ottensmeier
    • 4
  • Sjoerd H. van der Burg
    • 3
  • Cedrik M. Britten
    • 5
  • Cliburn Chan
    • 6
    Email author
  1. 1.Department of Immunology, Institute for Cell BiologyUniversity of TübingenTübingenGermany
  2. 2.Immatics Biotechnologies GmbHTuebingenGermany
  3. 3.Experimental Cancer Immunology and Therapy, Department of Clinical Oncology (K1-P)Leiden University Medical CenterLeidenThe Netherlands
  4. 4.University of SouthamptonSouthamptonUK
  5. 5.TRONTranslational Oncology at the University Medical Center of the Johannes-Gutenberg University gGmbH and Association for Cancer Immunotherapy (CIMT)MainzGermany
  6. 6.Department of Biostatistics and BioinformaticsDuke University Medical CenterDurhamUSA

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