Decoding cancer cell death-driven immune cell recruitment: An in vivo method for site-of-vaccination analyses

Methods Enzymol. 2020:636:185-207. doi: 10.1016/bs.mie.2019.04.013. Epub 2019 May 2.

Abstract

Anticancer vaccines have recently received renewed attention for immunotherapy of at least a subset of cancer-types. Such vaccines mostly involve either killed cancer or tumor cells alone, or combinations thereof with specific (co-incubated) innate immune cells. In recent years, the immunogenic characteristics of the dead or dying cancer cells have emerged as decisive factors behind the success of anticancer vaccines. This has amplified the importance of accounting for immunology of cell death while preparing anticancer vaccines. This, in turn, has increased the emphasis on the immune reactions at the site-of-vaccination since the therapeutic efficacy of the killed cancer/tumor cell vaccines is contingent upon the nature and characteristics of these reactions at the site-of-injection. In this article, we present a systematic methodology that exploits the murine ear pinna model to study differential immune cell recruitment by dead/dying cancer cells injected in vivo, thereby modeling the site-of-injection relevant for anticancer vaccines.

Keywords: Apoptosis; Danger signals; Dendritic cells; Immunogenic cell death (ICD); Immunotherapy; Innate immunity; Macrophages; Necroptosis; Necrosis; Neutrophils.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cancer Vaccines*
  • Cell Death
  • Immunotherapy
  • Mice
  • Neoplasms* / therapy
  • Vaccination

Substances

  • Cancer Vaccines