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Trial watch: chemotherapy-induced immunogenic cell death in oncology.

Authors :
Sprooten J
Laureano RS
Vanmeerbeek I
Govaerts J
Naulaerts S
Borras DM
Kinget L
Fucíková J
Špíšek R
Jelínková LP
Kepp O
Kroemer G
Krysko DV
Coosemans A
Vaes RDW
De Ruysscher D
De Vleeschouwer S
Wauters E
Smits E
Tejpar S
Beuselinck B
Hatse S
Wildiers H
Clement PM
Vandenabeele P
Zitvogel L
Garg AD
Source :
Oncoimmunology [Oncoimmunology] 2023 Jun 03; Vol. 12 (1), pp. 2219591. Date of Electronic Publication: 2023 Jun 03 (Print Publication: 2023).
Publication Year :
2023

Abstract

Immunogenic cell death (ICD) refers to an immunologically distinct process of regulated cell death that activates, rather than suppresses, innate and adaptive immune responses. Such responses culminate into T cell-driven immunity against antigens derived from dying cancer cells. The potency of ICD is dependent on the immunogenicity of dying cells as defined by the antigenicity of these cells and their ability to expose immunostimulatory molecules like damage-associated molecular patterns (DAMPs) and cytokines like type I interferons (IFNs). Moreover, it is crucial that the host's immune system can adequately detect the antigenicity and adjuvanticity of these dying cells. Over the years, several well-known chemotherapies have been validated as potent ICD inducers, including (but not limited to) anthracyclines, paclitaxels, and oxaliplatin. Such ICD-inducing chemotherapeutic drugs can serve as important combinatorial partners for anti-cancer immunotherapies against highly immuno-resistant tumors. In this Trial Watch, we describe current trends in the preclinical and clinical integration of ICD-inducing chemotherapy in the existing immuno-oncological paradigms.<br />Competing Interests: No potential conflict of interest was reported by the authors.<br /> (© 2023 The Author(s). Published with license by Taylor & Francis Group, LLC.)

Details

Language :
English
ISSN :
2162-402X
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Oncoimmunology
Publication Type :
Academic Journal
Accession number :
37284695
Full Text :
https://doi.org/10.1080/2162402X.2023.2219591