Immunogenic Apoptosis as a Novel Tool for Anticancer Vaccine Development

被引:101
作者
Montico, Barbara [1 ]
Nigro, Annunziata [2 ]
Casolaro, Vincenzo [2 ]
Dal Col, Jessica [2 ]
机构
[1] Ctr Riferimento Oncol, Dept Translat Res Immunopathol & Canc Biomarkers, I-33081 Aviano, PN, Italy
[2] Univ Salerno, Dept Med Surg & Dent, Scuola Med Salernitana, I-84081 Baronissi, SA, Italy
关键词
immunogenic cell death; DAMP; calreticulin; DC-based vaccine; NF-KAPPA-B; HEAT-SHOCK PROTEINS; DENDRITIC CELLS; CALRETICULIN EXPOSURE; PHOTODYNAMIC THERAPY; TUMOR-CELLS; IMMUNE-RESPONSES; ONCOLYTIC ADENOVIRUS; ATP SECRETION; T-CELLS;
D O I
10.3390/ijms19020594
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Immunogenic apoptosis, or more appropriately called immunogenic cell death (ICD), is a recently described form of apoptosis induced by a specific set of chemotherapeutic drugs or by physical therapeutic modalities, such as ionizing irradiation and photodynamic therapy. The peculiar characteristic of ICD is the ability to favor recognition and elimination of dying tumor cells by phagocytes in association with the release of pro-inflammatory molecules (such as cytokines and high-mobility group box-1). While in vitro and animal models pointed to ICD as one of the molecular mechanisms mediating the clinical efficacy of some anticancer agents, it is hard to clearly demonstrate its contribution in cancer patients. Clinical evidence suggests that the induction of ICD alone is possibly not sufficient to fully subvert the immunosuppressive tumor microenvironment. However, interesting results from recent studies contemplate the exploitation of ICD for improving the immunogenicity of cancer cells to use them as an antigen cargo in the development of dendritic cell (DC) vaccines. Herein, we discuss the effects of danger signals expressed or released by cancer cells undergoing ICD on the maturation and activation of immature and mature DC, highlighting the potential added value of ICD in adoptive immunotherapy protocols.
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页数:16
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共 93 条
[71]   The EGFR-specific antibody cetuximab combined with chemotherapy triggers immunogenic cell death [J].
Pozzi, Chiara ;
Cuomo, Alessandro ;
Spadoni, Ilaria ;
Magni, Elena ;
Silvola, Alessio ;
Conte, Alexia ;
Sigismund, Sara ;
Ravenda, Paola Simona ;
Bonaldi, Tiziana ;
Zampino, Maria Giulia ;
Cancelliere, Carlotta ;
Di Fiore, Pier Paolo ;
Bardelli, Alberto ;
Penna, Giuseppe ;
Rescigno, Maria .
NATURE MEDICINE, 2016, 22 (06) :624-+
[72]   Dendritic cell survival and maturation are regulated by different signaling pathways [J].
Rescigno, M ;
Martino, M ;
Sutherland, CL ;
Gold, MR ;
Ricciardi-Castagnoli, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (11) :2175-2180
[73]   GSK-3 mediates differentiation and activation of proinflammatory dendritic cells [J].
Rodionova, Elena ;
Conzelmann, Michael ;
Maraskovsky, Eugene ;
Hess, Michael ;
Kirsch, Michael ;
Giese, Thomas ;
ho, Antny D. Ho ;
Zoeller, Margot ;
Dreger, Peter ;
Luft, Thomas .
BLOOD, 2007, 109 (04) :1584-1592
[74]   Low dose hypericin-PDT induces complete tumor regression in BALB/c mice bearing CT26 colon carcinoma [J].
Sanovic, Renata ;
Verwanger, Thomas ;
Hartl, Arnulf ;
Krammer, Barbara .
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2011, 8 (04) :291-296
[75]   Release of chromatin protein HMGB1 by necrotic cells triggers inflammation [J].
Scaffidi, P ;
Misteli, T ;
Bianchi, ME .
NATURE, 2002, 418 (6894) :191-195
[76]   Control of RelB during dendritic cell activation integrates canonical and noncanonical NF-κB pathways [J].
Shih, Vincent F-S ;
Davis-Turak, Jeremy ;
Macal, Monica ;
Huang, Jenny Q. ;
Ponomarenko, Julia ;
Kearns, Jeffrey D. ;
Yu, Tony ;
Fagerlund, Riku ;
Asagiri, Masataka ;
Zuniga, Elina I. ;
Hoffmann, Alexander .
NATURE IMMUNOLOGY, 2012, 13 (12) :1162-+
[77]   Cancer cell-autonomous contribution of type I interferon signaling to the efficacy of chemotherapy [J].
Sistigu, Antonella ;
Yamazaki, Takahiro ;
Vacchelli, Erika ;
Chaba, Kariman ;
Enot, David P. ;
Adam, Julien ;
Vitale, Ilio ;
Goubar, Aicha ;
Baracco, Elisa E. ;
Remedios, Catarina ;
Fend, Laetitia ;
Hannani, Dalil ;
Aymeric, Laetitia ;
Ma, Yuting ;
Niso-Santano, Mireia ;
Kepp, Oliver ;
Schultze, Joachim L. ;
Tueting, Thomas ;
Belardelli, Filippo ;
Bracci, Laura ;
La Sorsa, Valentina ;
Ziccheddu, Giovanna ;
Sestili, Paola ;
Urbani, Francesca ;
Delorenzi, Mauro ;
Lacroix-Triki, Magali ;
Quidville, Virginie ;
Conforti, Rosa ;
Spano, Jean-Philippe ;
Pusztai, Lajos ;
Poirier-Colame, Vichnou ;
Delaloge, Suzette ;
Penault-Llorca, Frederique ;
Ladoire, Sylvain ;
Arnould, Laurent ;
Cyrta, Joanna ;
Dessoliers, Marie-Charlotte ;
Eggermont, Alexander ;
Bianchi, Marco E. ;
Pittet, Mikael ;
Engblom, Camilla ;
Pfirschke, Christina ;
Preville, Xavier ;
Uze, Gilles ;
Schreiber, Robert D. ;
Chow, Melvyn T. ;
Smyth, Mark J. ;
Proietti, Enrico ;
Andre, Fabrice ;
Kroemer, Guido .
NATURE MEDICINE, 2014, 20 (11) :1301-1309
[78]   Towards a better way to die with chemotherapy - Role of heat shock protein exposure on dying tumor cells [J].
Spisek, Radek ;
Dhodapkar, Madhav V. .
CELL CYCLE, 2007, 6 (16) :1962-1965
[79]   Bortezomib enhances dendritic cell (DC)-mediated induction of immunity to human myeloma via exposure of cell surface heat shock protein 90 on dying tumor cells: therapeutic implications [J].
Spisek, Radek ;
Charalambous, Anna ;
Mazumder, Amitabha ;
Vesole, David H. ;
Jagannath, Sundar ;
Dhodapkar, Madhav V. .
BLOOD, 2007, 109 (11) :4839-4845
[80]   Calreticulin expression: Interaction with the immune infiltrate and impact on survival in patients with ovarian and non-small cell lung cancer [J].
Stoll, Gautier ;
Iribarren, Kristina ;
Michels, Judith ;
Leary, Alexandra ;
Zitvogel, Laurence ;
Cremer, Isabelle ;
Kroemer, Guido .
ONCOIMMUNOLOGY, 2016, 5 (07)