Immunogenic Cell Death in Cancer Therapy

Author:

Kroemer Guido12345,Galluzzi Lorenzo65,Kepp Oliver167,Zitvogel Laurence897

Affiliation:

1. U848,

2. Metabolomics Platform,

3. Equipe 11 Labellisée par la Ligue Nationale Contre le Cancer, Centre de Recherche des Cordeliers, 75006 Paris, France

4. Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP, 75015 Paris, France

5. Université Paris Descartes/V, Sorbonne Paris Cité, 75006 Paris, France

6. Institut Gustave Roussy, 94805 Villejuif, France

7. Université Paris Sud/XI, 94805 Villejuif, France

8. U1015, INSERM, 94805 Villejuif, France;

9. Center of Clinical Investigations, Institut Gustave Roussy, 94805 Villejuif, France

Abstract

Depending on the initiating stimulus, cancer cell death can be immunogenic or nonimmunogenic. Immunogenic cell death (ICD) involves changes in the composition of the cell surface as well as the release of soluble mediators, occurring in a defined temporal sequence. Such signals operate on a series of receptors expressed by dendritic cells to stimulate the presentation of tumor antigens to T cells. We postulate that ICD constitutes a prominent pathway for the activation of the immune system against cancer, which in turn determines the long-term success of anticancer therapies. Hence, suboptimal regimens (failing to induce ICD), selective alterations in cancer cells (preventing the emission of immunogenic signals during ICD), or defects in immune effectors (abolishing the perception of ICD by the immune system) can all contribute to therapeutic failure. We surmise that ICD and its subversion by pathogens also play major roles in antiviral immune responses.

Publisher

Annual Reviews

Subject

Immunology,Immunology and Allergy

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