Immunogenic cell death (ICD) enhancers—Drugs that enhance the perception of ICD by dendritic cells

Author:

Liu Peng12,Zhao Liwei12,Zitvogel Laurence345ORCID,Kepp Oliver12,Kroemer Guido126ORCID

Affiliation:

1. Centre de Recherche des Cordeliers, Equipe Labellisée par la Ligue Contre le Cancer Université de Paris Cité, Sorbonne Université, Inserm U1138, Institut Universitaire de France Paris France

2. Metabolomics and Cell Biology Platforms Gustave Roussy Cancer Center Villejuif France

3. INSERM U1015 Equipe Labellisée – Ligue Nationale contre le Cancer Villejuif France

4. Gustave Roussy ClinicObiome Villejuif France

5. Center of Clinical Investigations in Biotherapies of Cancer (CICBT) 1428 Villejuif France

6. Department of Biology, Institut du Cancer Paris CARPEM Hôpital Européen Georges Pompidou, AP‐HP Paris France

Abstract

SummaryThe search for immunostimulatory drugs applicable to cancer immunotherapy may profit from target‐agnostic methods in which agents are screened for their functional impact on immune cells cultured in vitro without any preconceived idea on their mode of action. We have built a synthetic mini‐immune system in which stressed and dying cancer cells (derived from standardized cell lines) are confronted with dendritic cells (DCs, derived from immortalized precursors) and CD8+ T‐cell hybridoma cells expressing a defined T‐cell receptor. Using this system, we can identify three types of immunostimulatory drugs: (i) pharmacological agents that stimulate immunogenic cell death (ICD) of malignant cells; (ii) drugs that act on DCs to enhance their response to ICD; and (iii) drugs that act on T cells to increase their effector function. Here, we focus on strategies to develop drugs that enhance the perception of ICD by DCs and to which we refer as “ICD enhancers.” We discuss examples of ICD enhancers, including ligands of pattern recognition receptors (exemplified by TLR3 ligands that correct the deficient function of DCs lacking FPR1) and immunometabolic modifiers (exemplified by hexokinase‐2 inhibitors), as well as methods for target deconvolution applicable to the mechanistic characterization of ICD enhancers.

Funder

Ligue Contre le Cancer

Agence Nationale de la Recherche

Fondation pour la Recherche Médicale

CNIB

Institut Universitaire de France

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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