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Molecular and Translational Classifications of DAMPs in Immunogenic Cell Death.

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  1. Galluzzi Lorenzo, Vacchelli Erika, Pedro José-Manuel Bravo-San, Buqué Aitziber, Senovilla Laura, Baracco Elisa Elena, Bloy Norma, Castoldi Francesca, Abastado Jean-Pierre, Agostinis Patrizia, Apte Ron N., Aranda Fernando, Ayyoub Maha, Beckhove Philipp, Blay Jean-Yves, Bracci Laura, Caignard Anne, Castelli Chiara, Cavallo Federica, Celis Estaban, Cerundolo Vincenzo, Clayton Aled, Colombo Mario P., Coussens Lisa, Dhodapkar Madhav V., Eggermont Alexander M., Fearon Douglas T., Fridman Wolf H., Fučíková Jitka, Gabrilovich Dmitry I., Galon Jérôme, Garg Abhishek, Ghiringhelli François, Giaccone Giuseppe, Gilboa Eli, Gnjatic Sacha, Hoos Axel, Hosmalin Anne, Jäger Dirk, Kalinski Pawel, Kärre Klas, Kepp Oliver, Kiessling Rolf, Kirkwood John M., Klein Eva, Knuth Alexander, Lewis Claire E., Liblau Roland, Lotze Michael T., Lugli Enrico, Mach Jean-Pierre, Mattei Fabrizio, Mavilio Domenico, Melero Ignacio, Melief Cornelis J., Mittendorf Elizabeth A., Moretta Lorenzo, Odunsi Adekunke, Okada Hideho, Palucka Anna Karolina, Peter Marcus E., Pienta Kenneth J., Porgador Angel, Prendergast George C., Rabinovich Gabriel A., Restifo Nicholas P., Rizvi Naiyer, Sautès-Fridman Catherine, Schreiber Hans, Seliger Barbara, Shiku Hiroshi, Silva-Santos Bruno, Smyth Mark J., Speiser Daniel E., Spisek Radek, Srivastava Pramod K., Talmadge James E., Tartour Eric, Van Der Burg Sjoerd H., Eynde Benoît J. Van Den, Vile Richard, Wagner Hermann, Weber Jeffrey  S., Whiteside Theresa L., Wolchok Jedd D., Zitvogel Laurence, Zou Weiping, Kroemer Guido, Classification of current anticancer immunotherapies, 10.18632/oncotarget.2998
  2. Kepp Oliver, Tesniere Antoine, Zitvogel Laurence, Kroemer Guido, The immunogenicity of tumor cell death : , 10.1097/cco.0b013e32831bc375
  3. Garg Abhishek D., Dudek Aleksandra M., Agostinis Patrizia, Cancer immunogenicity, danger signals, and DAMPs: What, when, and how? : Danger signaling, DAMPs, and Cancer, 10.1002/biof.1125
  4. Blankenstein Thomas, Coulie Pierre G., Gilboa Eli, Jaffee Elizabeth M., The determinants of tumour immunogenicity, 10.1038/nrc3246
  5. Garg Abhishek D., Nowis Dominika, Golab Jakub, Vandenabeele Peter, Krysko Dmitri V., Agostinis Patrizia, Immunogenic cell death, DAMPs and anticancer therapeutics: An emerging amalgamation, 10.1016/j.bbcan.2009.08.003
  6. Anguille Sébastien, Smits Evelien L, Lion Eva, van Tendeloo Viggo F, Berneman Zwi N, Clinical use of dendritic cells for cancer therapy, 10.1016/s1470-2045(13)70585-0
  7. Chiang Cheryl Lai-Lai, Kandalaft Lana E., Coukos George, Adjuvants for Enhancing the Immunogenicity of Whole Tumor Cell Vaccines, 10.3109/08830185.2011.572210
  8. Parish Christopher R, Cancer immunotherapy: The past, the present and the future, 10.1046/j.0818-9641.2003.01151.x
  9. COLEY WILLIAM B., THE TREATMENT OF MALIGNAT TUMORS BY REPEATED INOCULATIONS OF ERYSIPELAS : WITH A REPORT OF TEN ORIGINAL CASES, 10.1097/00000441-189305000-00001
  10. Tsung Kangla, Norton Jeffrey A., Lessons from Coley's Toxin, 10.1016/j.suronc.2006.05.002
  11. Coulie Pierre G., Van den Eynde Benoît J., van der Bruggen Pierre, Boon Thierry, Tumour antigens recognized by T lymphocytes: at the core of cancer immunotherapy, 10.1038/nrc3670
  12. Liao S.K., Carr D.H., Comparative immunogenicity of irradiated, neuraminidase treated, and fused cells of a strain-restricted sarcoma, 10.1007/bf00284498
  13. Milas Luka, Withers H. Rodney, Nonspecific Immunotherapy of Malignant Tumors, 10.1148/118.1.211
  14. Bogden, Natl Cancer Inst Monogr, 97 (1978)
  15. Dickson, Natl Cancer Inst Monogr, 61, 183 (1982)
  16. Suit, Br J Cancer Suppl, 4, 1 (1980)
  17. Richert Lysiane, Or Ayala, Shinitzky Meir, Promotion of tumor antigenicity in EL-4 leukemia cells by hydrostatic pressure, 10.1007/bf00199125
  18. Galluzzi Lorenzo, Senovilla Laura, Zitvogel Laurence, Kroemer Guido, The secret ally: immunostimulation by anticancer drugs, 10.1038/nrd3626
  19. Green Douglas R., Ferguson Thomas, Zitvogel Laurence, Kroemer Guido, Immunogenic and tolerogenic cell death, 10.1038/nri2545
  20. Matzinger P, Tolerance, Danger, and the Extended Family, 10.1146/annurev.iy.12.040194.005015
  21. Matzinger P., The Danger Model: A Renewed Sense of Self, 10.1126/science.1071059
  22. Land Walter, Schneeberger Helmut, Schleibner Stefan, Illner Wolf-Dieter, Abendroth Dietmar, Rutili Gianfranco, Arfors Karl E., Messmer Konrad, THE BENEFICIAL EFFECT OF HUMAN RECOMBINANT SUPEROXIDE DISMUTASE ON ACUTE AND CHRONIC REJECTION EVENTS IN RECIPIENTS OF CADAVERIC RENAL TRANSPLANTS : , 10.1097/00007890-199401001-00010
  23. Seong Seung-Yong, Matzinger Polly, Hydrophobicity: an ancient damage-associated molecular pattern that initiates innate immune responses, 10.1038/nri1372
  24. Rubartelli Anna, Lotze Michael T., Inside, outside, upside down: damage-associated molecular-pattern molecules (DAMPs) and redox, 10.1016/j.it.2007.08.004
  25. Li Guanqiao, Tang Daolin, Lotze Michael T., Ménage à Trois in stress: DAMPs, redox and autophagy, 10.1016/j.semcancer.2013.08.002
  26. Garg A D, Martin S, Golab J, Agostinis P, Danger signalling during cancer cell death: origins, plasticity and regulation, 10.1038/cdd.2013.48
  27. Bianchi Marco E., DAMPs, PAMPs and alarmins: all we need to know about danger, 10.1189/jlb.0306164
  28. Bondanza Attilio, Zimmermann Valérie S., Rovere-Querini Patrizia, Turnay Javier, Dumitriu Ingrid E., Stach Christian M., Voll Reinhard E., Gaipl Udo S., Bertling Wolf, Pöschl Ernst, Kalden Joachim R., Manfredi Angelo A., Herrmann Martin, Inhibition of Phosphatidylserine Recognition Heightens the Immunogenicity of Irradiated Lymphoma Cells In Vivo, 10.1084/jem.20040327
  29. Stach C M, Turnay X, Voll R E, Kern P M, Kolowos W, Beyer T D, Kalden J R, Herrmann M, Treatment with annexin V increases immunogenicity of apoptotic human T-cells in Balb/c mice, 10.1038/sj.cdd.4400715
  30. Dudek-Peri  A. M., Ferreira G. B., Muchowicz A., Wouters J., Prada N., Martin S., Kiviluoto S., Winiarska M., Boon L., Mathieu C., van den Oord J., Stas M., Gougeon M.-L., Golab J., Garg A. D., Agostinis P., Antitumor Immunity Triggered by Melphalan Is Potentiated by Melanoma Cell Surface-Associated Calreticulin, 10.1158/0008-5472.can-14-2089
  31. Rondas Dieter, Crèvecoeur Inne, D’Hertog Wannes, Ferreira Gabriela Bomfim, Staes An, Garg Abhishek D., Eizirik Decio L., Agostinis Patrizia, Gevaert Kris, Overbergh Lut, Mathieu Chantal, Citrullinated Glucose-Regulated Protein 78 Is an Autoantigen in Type 1 Diabetes, 10.2337/db14-0621
  32. Venereau Emilie, Casalgrandi Maura, Schiraldi Milena, Antoine Daniel J., Cattaneo Angela, De Marchis Francesco, Liu Jaron, Antonelli Antonella, Preti Alessandro, Raeli Lorenzo, Shams Sara Samadi, Yang Huan, Varani Luca, Andersson Ulf, Tracey Kevin J., Bachi Angela, Uguccioni Mariagrazia, Bianchi Marco E., Mutually exclusive redox forms of HMGB1 promote cell recruitment or proinflammatory cytokine release, 10.1084/jem.20120189
  33. Weyd Heiko, Abeler-Dörner Lucie, Linke Björn, Mahr Andrea, Jahndel Veronika, Pfrang Sandra, Schnölzer Martina, Falk Christine S., Krammer Peter H., Annexin A1 on the Surface of Early Apoptotic Cells Suppresses CD8+ T Cell Immunity, 10.1371/journal.pone.0062449
  34. Garg Abhishek D., Dudek Aleksandra M., Ferreira Gabriela B., Verfaillie Tom, Vandenabeele Peter, Krysko Dmitri V., Mathieu Chantal, Agostinis Patrizia, ROS-induced autophagy in cancer cells assists in evasion from determinants of immunogenic cell death, 10.4161/auto.25399
  35. Garg Abhishek D, Krysko Dmitri V, Verfaillie Tom, Kaczmarek Agnieszka, Ferreira Gabriela B, Marysael Thierry, Rubio Noemi, Firczuk Malgorzata, Mathieu Chantal, Roebroek Anton J M, Annaert Wim, Golab Jakub, de Witte Peter, Vandenabeele Peter, Agostinis Patrizia, A novel pathway combining calreticulin exposure and ATP secretion in immunogenic cancer cell death : CRT, ATP, and immunogenic cancer cell death, 10.1038/emboj.2011.497
  36. Ghiringhelli François, Apetoh Lionel, Tesniere Antoine, Aymeric Laetitia, Ma Yuting, Ortiz Carla, Vermaelen Karim, Panaretakis Theocharis, Mignot Grégoire, Ullrich Evelyn, Perfettini Jean-Luc, Schlemmer Frédéric, Tasdemir Ezgi, Uhl Martin, Génin Pierre, Civas Ahmet, Ryffel Bernhard, Kanellopoulos Jean, Tschopp Jürg, André Fabrice, Lidereau Rosette, McLaughlin Nicole M, Haynes Nicole M, Smyth Mark J, Kroemer Guido, Zitvogel Laurence, Activation of the NLRP3 inflammasome in dendritic cells induces IL-1β–dependent adaptive immunity against tumors, 10.1038/nm.2028
  37. Elliott Michael R., Chekeni Faraaz B., Trampont Paul C., Lazarowski Eduardo R., Kadl Alexandra, Walk Scott F., Park Daeho, Woodson Robin I., Ostankovich Marina, Sharma Poonam, Lysiak Jeffrey J., Harden T. Kendall, Leitinger Norbert, Ravichandran Kodi S., Nucleotides released by apoptotic cells act as a find-me signal to promote phagocytic clearance, 10.1038/nature08296
  38. Iwata Akiko, Morgan-Stevenson Vicki, Schwartz Barbara, Liu Li, Tupper Joan, Zhu Xiaodong, Harlan John, Winn Robert, Extracellular BCL2 Proteins Are Danger-Associated Molecular Patterns That Reduce Tissue Damage in Murine Models of Ischemia-Reperfusion Injury, 10.1371/journal.pone.0009103
  39. Babelova Andrea, Moreth Kristin, Tsalastra-Greul Wasiliki, Zeng-Brouwers Jinyang, Eickelberg Oliver, Young Marian F., Bruckner Peter, Pfeilschifter Josef, Schaefer Roland M., Gröne Hermann-Josef, Schaefer Liliana, Biglycan, a Danger Signal That Activates the NLRP3 Inflammasome via Toll-like and P2X Receptors, 10.1074/jbc.m109.014266
  40. Schaefer Liliana, Extracellular matrix molecules: endogenous danger signals as new drug targets in kidney diseases, 10.1016/j.coph.2009.11.007
  41. Obeid Michel, Tesniere Antoine, Ghiringhelli François, Fimia Gian Maria, Apetoh Lionel, Perfettini Jean-Luc, Castedo Maria, Mignot Grégoire, Panaretakis Theoharis, Casares Noelia, Métivier Didier, Larochette Nathanael, van Endert Peter, Ciccosanti Fabiola, Piacentini Mauro, Zitvogel Laurence, Kroemer Guido, Calreticulin exposure dictates the immunogenicity of cancer cell death, 10.1038/nm1523
  42. Garg Abhishek D., Elsen Sanne, Krysko Dmitri V., Vandenabeele Peter, de Witte Peter, Agostinis Patrizia, Resistance to anticancer vaccination effect is controlled by a cancer cell-autonomous phenotype that disrupts immunogenic phagocytic removal, 10.18632/oncotarget.4754
  43. Koks Carolien A., Garg Abhishek D., Ehrhardt Michael, Riva Matteo, Vandenberk Lien, Boon Louis, Vleeschouwer Steven De, Agostinis Patrizia, Graf Norbert, Van Gool Stefaan W., Newcastle disease virotherapy induces long-term survival and tumor-specific immune memory in orthotopic glioma through the induction of immunogenic cell death : Newcastle disease virotherapy induces antitumor immunity, 10.1002/ijc.29202
  44. Gardai Shyra J., McPhillips Kathleen A., Frasch S. Courtney, Janssen William J., Starefeldt Anna, Murphy-Ullrich Joanne E., Bratton Donna L., Oldenborg Per-Arne, Michalak Marek, Henson Peter M., Cell-Surface Calreticulin Initiates Clearance of Viable or Apoptotic Cells through trans-Activation of LRP on the Phagocyte, 10.1016/j.cell.2005.08.032
  45. Garcia Fernandez, Cell Growth Differ, 13, 449 (2002)
  46. Sorice M, Circella A, Cristea I M, Garofalo T, Renzo L Di, Alessandri C, Valesini G, Esposti M Degli, Cardiolipin and its metabolites move from mitochondria to other cellular membranes during death receptor-mediated apoptosis, 10.1038/sj.cdd.4401457
  47. Korbelik Mladen, Banáth Judit, Sun Jinghai, Canals Daniel, Hannun Yusuf A., Separovic Duska, Ceramide and sphingosine-1-phosphate act as photodynamic therapy-elicited damage-associated molecular patterns: Cell surface exposure, 10.1016/j.intimp.2014.03.016
  48. Horino, Lab Invest, 78, 603 (1998)
  49. Nishimura T., Horino K., Nishiura H., Shibuya Y., Hiraoka T., Tanase S., Yamamoto T., Apoptotic Cells of an Epithelial Cell Line, AsPC-1, Release Monocyte Chemotactic S19 Ribosomal Protein Dimer, 10.1093/oxfordjournals.jbchem.a002876
  50. Peter Christoph, Wesselborg Sebastian, Kirsten Lauber, Role of Attraction and Danger Signals in the Uptake of Apoptotic and Necrotic Cells and its Immunological Outcome, Phagocytosis of Dying Cells: From Molecular Mechanisms to Human Diseases ISBN:9781402092923 p.63-101, 10.1007/978-1-4020-9293-0_3
  51. Yamamoto Tetsuro, Roles of the ribosomal protein S19 dimer and the C5a receptor in pathophysiological functions of phagocytic leukocytes, 10.1111/j.1440-1827.2007.02049.x
  52. Struck, Shock, 23, 533 (2005)
  53. Krysko Dmitri V., Garg Abhishek D., Kaczmarek Agnieszka, Krysko Olga, Agostinis Patrizia, Vandenabeele Peter, Immunogenic cell death and DAMPs in cancer therapy, 10.1038/nrc3380
  54. Pullerits R., Bokarewa M., Jonsson I.-M., Verdrengh M., Tarkowski A., Extracellular cytochrome c, a mitochondrial apoptosis-related protein, induces arthritis, 10.1093/rheumatology/keh406
  55. Codina Ramil, Vanasse Amelia, Kelekar Ameeta, Vezys Vaiva, Jemmerson Ronald, Cytochrome c-induced lymphocyte death from the outside in: inhibition by serum leucine-rich alpha-2-glycoprotein-1, 10.1007/s10495-009-0412-0
  56. Yoon K. W., Byun S., Kwon E., Hwang S.-Y., Chu K., Hiraki M., Jo S.-H., Weins A., Hakroush S., Cebulla A., Sykes D. B., Greka A., Mundel P., Fisher D. E., Mandinova A., Lee S. W., Control of signaling-mediated clearance of apoptotic cells by the tumor suppressor p53, 10.1126/science.1261669
  57. Kao, J Biol Chem, 269, 25106 (1994)
  58. Knies U. E., Behrensdorf H. A., Mitchell C. A., Deutsch U., Risau W., Drexler H. C. A., Clauss M., Regulation of endothelial monocyte-activating polypeptide II release by apoptosis, 10.1073/pnas.95.21.12322
  59. Ahrens Susan, Zelenay Santiago, Sancho David, Hanč Pavel, Kjær Svend, Feest Christoph, Fletcher Georgina, Durkin Charlotte, Postigo Antonio, Skehel Mark, Batista Facundo, Thompson Barry, Way Michael, Reis e Sousa Caetano, Schulz Oliver, F-Actin Is an Evolutionarily Conserved Damage-Associated Molecular Pattern Recognized by DNGR-1, a Receptor for Dead Cells, 10.1016/j.immuni.2012.03.008
  60. Chiba Shigeki, Baghdadi Muhammad, Akiba Hisaya, Yoshiyama Hironori, Kinoshita Ichiro, Dosaka-Akita Hirotoshi, Fujioka Yoichiro, Ohba Yusuke, Gorman Jacob V, Colgan John D, Hirashima Mitsuomi, Uede Toshimitsu, Takaoka Akinori, Yagita Hideo, Jinushi Masahisa, Tumor-infiltrating DCs suppress nucleic acid–mediated innate immune responses through interactions between the receptor TIM-3 and the alarmin HMGB1, 10.1038/ni.2376
  61. Zitvogel Laurence, Kepp Oliver, Kroemer Guido, Decoding Cell Death Signals in Inflammation and Immunity, 10.1016/j.cell.2010.02.015
  62. Pletjushkina O Yu, Fetisova E K, Lyamzaev K G, Ivanova O Yu, Domnina L V, Vyssokikh M Yu, Pustovidko A V, Vasiliev J M, Murphy M P, Chernyak B V, Skulachev V P, Long-distance apoptotic killing of cells is mediated by hydrogen peroxide in a mitochondrial ROS-dependent fashion, 10.1038/sj.cdd.4401685
  63. Garg Abhishek D., Nowis Dominika, Golab Jakub, Agostinis Patrizia, Photodynamic therapy: illuminating the road from cell death towards anti-tumour immunity, 10.1007/s10495-010-0479-7
  64. Suzuki Shigeki, Kulkarni Ashok B., Extracellular heat shock protein HSP90β secreted by MG63 osteosarcoma cells inhibits activation of latent TGF-β1, 10.1016/j.bbrc.2010.06.112
  65. Korbelik, Cancer Res, 65, 1018 (2005)
  66. Cirone Mara, Di Renzo Livia, Lotti Lavinia Vittoria, Conte Valeria, Trivedi Pankaj, Santarelli Roberta, Gonnella Roberta, Frati Luigi, Faggioni Alberto, Primary Effusion Lymphoma Cell Death Induced by Bortezomib and AG 490 Activates Dendritic Cells through CD91, 10.1371/journal.pone.0031732
  67. Zunino B, Rubio-Patiño C, Villa E, Meynet O, Proics E, Cornille A, Pommier S, Mondragón L, Chiche J, Bereder J-M, Carles M, Ricci J-E, Hyperthermic intraperitoneal chemotherapy leads to an anticancer immune response via exposure of cell surface heat shock protein 90, 10.1038/onc.2015.82
  68. Zhou Zhiwei, Yamamoto Yoichi, Sugai Fuminobu, Yoshida Kenya, Kishima Yoshihiko, Sumi Hisae, Nakamura Hideji, Sakoda Saburo, Hepatoma-derived Growth Factor Is a Neurotrophic Factor Harbored in the Nucleus, 10.1074/jbc.m308650200
  69. Huang Hai, Evankovich John, Yan Wei, Nace Gary, Zhang Lemeng, Ross Mark, Liao Xinghua, Billiar Timothy, Xu Jun, Esmon Charles T., Tsung Allan, Endogenous histones function as alarmins in sterile inflammatory liver injury through Toll-like receptor 9 in mice, 10.1002/hep.24501
  70. Apetoh Lionel, Ghiringhelli François, Tesniere Antoine, Obeid Michel, Ortiz Carla, Criollo Alfredo, Mignot Grégoire, Maiuri M Chiara, Ullrich Evelyn, Saulnier Patrick, Yang Huan, Amigorena Sebastian, Ryffel Bernard, Barrat Franck J, Saftig Paul, Levi Francis, Lidereau Rosette, Nogues Catherine, Mira Jean-Paul, Chompret Agnès, Joulin Virginie, Clavel-Chapelon Françoise, Bourhis Jean, André Fabrice, Delaloge Suzette, Tursz Thomas, Kroemer Guido, Zitvogel Laurence, Toll-like receptor 4–dependent contribution of the immune system to anticancer chemotherapy and radiotherapy, 10.1038/nm1622
  71. Semino C., NK/iDC interaction results in IL-18 secretion by DCs at the synaptic cleft followed by NK cell activation and release of the DC maturation factor HMGB1, 10.1182/blood-2004-10-3906
  72. Scaffidi Paola, Misteli Tom, Bianchi Marco E., Release of chromatin protein HMGB1 by necrotic cells triggers inflammation, 10.1038/nature00858
  73. Thorburn J, Horita H, Redzic J, Hansen K, Frankel A E, Thorburn A, Autophagy regulates selective HMGB1 release in tumor cells that are destined to die, 10.1038/cdd.2008.143
  74. Yang De, Postnikov Yuri V., Li Yana, Tewary Poonam, de la Rosa Gonzalo, Wei Feng, Klinman Dennis, Gioannini Theresa, Weiss Jerrold P., Furusawa Takashi, Bustin Michael, Oppenheim Joost J., High-mobility group nucleosome-binding protein 1 acts as an alarmin and is critical for lipopolysaccharide-induced immune responses, 10.1084/jem.20101354
  75. Cohen I., Rider P., Carmi Y., Braiman A., Dotan S., White M. R., Voronov E., Martin M. U., Dinarello C. A., Apte R. N., Differential release of chromatin-bound IL-1  discriminates between necrotic and apoptotic cell death by the ability to induce sterile inflammation, 10.1073/pnas.0915018107
  76. Vanden Berghe Tom, Kalai Michael, Denecker Geertrui, Meeus Ann, Saelens Xavier, Vandenabeele Peter, Necrosis is associated with IL-6 production but apoptosis is not, 10.1016/j.cellsig.2005.05.003
  77. Lauber Kirsten, Bohn Erwin, Kröber Stefan Martin, Xiao Yi-jin, Blumenthal Sibylle G., Lindemann Ralph K., Marini Patrizia, Wiedig Carolin, Zobywalski Anke, Baksh Shairaz, Xu Yan, Autenrieth Ingo B., Schulze-Osthoff Klaus, Belka Claus, Stuhler Gernot, Wesselborg Sebastian, Apoptotic Cells Induce Migration of Phagocytes via Caspase-3-Mediated Release of a Lipid Attraction Signal, 10.1016/s0092-8674(03)00422-7
  78. Zhang Qin, Raoof Mustafa, Chen Yu, Sumi Yuka, Sursal Tolga, Junger Wolfgang, Brohi Karim, Itagaki Kiyoshi, Hauser Carl J., Circulating mitochondrial DAMPs cause inflammatory responses to injury, 10.1038/nature08780
  79. Collins L. Vincent, Hajizadeh Shahin, Holme Elisabeth, Jonsson Ing-Marie, Tarkowski Andrej, Endogenously oxidized mitochondrial DNA induces in vivo and in vitro inflammatory responses, 10.1189/jlb.0703328
  80. Galluzzi Lorenzo, Kepp Oliver, Kroemer Guido, Mitochondria: master regulators of danger signalling, 10.1038/nrm3479
  81. Shi Yan, Evans James E., Rock Kenneth L., Molecular identification of a danger signal that alerts the immune system to dying cells, 10.1038/nature01991
  82. Carp H., Mitochondrial N-formylmethionyl proteins as chemoattractants for neutrophils, 10.1084/jem.155.1.264
  83. RABIET M, HUET E, BOULAY F, The N-formyl peptide receptors and the anaphylatoxin C5a receptors: An overview, 10.1016/j.biochi.2007.02.015
  84. Czapiga Meggan, Gao Ji-Liang, Kirk Allan, Lekstrom-Himes Julie, Human platelets exhibit chemotaxis using functional N-formyl peptide receptors, 10.1016/j.exphem.2004.09.010
  85. Moghaddam A. E., Gartlan K. H., Kong L., Sattentau Q. J., Reactive Carbonyls Are a Major Th2-Inducing Damage-Associated Molecular Pattern Generated by Oxidative Stress, 10.4049/jimmunol.1003906
  86. Miller Y. I., Choi S.-H., Wiesner P., Fang L., Harkewicz R., Hartvigsen K., Boullier A., Gonen A., Diehl C. J., Que X., Montano E., Shaw P. X., Tsimikas S., Binder C. J., Witztum J. L., Oxidation-Specific Epitopes Are Danger-Associated Molecular Patterns Recognized by Pattern Recognition Receptors of Innate Immunity, 10.1161/circresaha.110.223875
  87. Vandenberk Lien, Garg Abhishek D., Verschuere Tina, Koks Carolien, Belmans Jochen, Beullens Monique, Agostinis Patrizia, De Vleeschouwer Steven, Van Gool Stefaan W., Irradiation of necrotic cancer cells, employed for pulsing dendritic cells (DCs), potentiates DC vaccine-induced antitumor immunity against high-grade glioma, 10.1080/2162402x.2015.1083669
  88. Riddell J. R., Wang X.-Y., Minderman H., Gollnick S. O., Peroxiredoxin 1 Stimulates Secretion of Proinflammatory Cytokines by Binding to TLR4, 10.4049/jimmunol.0901945
  89. Franz S, Herrmann K, Führnrohr B, Sheriff A, Frey B, Gaipl U S, Voll R E, Kalden J R, Jäck H-M, Herrmann M, After shrinkage apoptotic cells expose internal membrane-derived epitopes on their plasma membranes, 10.1038/sj.cdd.4402066
  90. Petrovski G, Zahuczky G, Katona K, Vereb G, Martinet W, Nemes Z, Bursch W, Fésüs L, Clearance of dying autophagic cells of different origin by professional and non-professional phagocytes, 10.1038/sj.cdd.4402112
  91. Bratton Donna L., Fadok Valerie A., Richter Donald A., Kailey Jenai M., Guthrie Lindsay A., Henson Peter M., Appearance of Phosphatidylserine on Apoptotic Cells Requires Calcium-mediated Nonspecific Flip-Flop and Is Enhanced by Loss of the Aminophospholipid Translocase, 10.1074/jbc.272.42.26159
  92. Martin S. J., Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis regardless of the initiating stimulus: inhibition by overexpression of Bcl-2 and Abl, 10.1084/jem.182.5.1545
  93. Brouckaert Greet, Kalai Michael, Krysko Dmitri V., Saelens Xavier, Vercammen Dominique, Ndlovu `Matladi, Haegeman Guy, D'Herde Katharina, Vandenabeele Peter, Phagocytosis of Necrotic Cells by Macrophages Is Phosphatidylserine Dependent and Does Not Induce Inflammatory Cytokine Production, 10.1091/mbc.e03-09-0668
  94. Donato Rosario, RAGE: A Single Receptor for Several Ligands and Different Cellular Responses: The Case of Certain S100 Proteins, 10.2174/156652407783220688
  95. Goh Fui G., Piccinini Anna M., Krausgruber Thomas, Udalova Irina A., Midwood Kim S., Transcriptional Regulation of the Endogenous Danger Signal Tenascin-C: A Novel Autocrine Loop in Inflammation, 10.4049/jimmunol.0903359
  96. Krispin A., Bledi Y., Atallah M., Trahtemberg U., Verbovetski I., Nahari E., Zelig O., Linial M., Mevorach D., Apoptotic cell thrombospondin-1 and heparin-binding domain lead to dendritic-cell phagocytic and tolerizing states, 10.1182/blood-2006-03-013334
  97. Galluzzi L, Bravo-San Pedro J M, Vitale I, Aaronson S A, Abrams J M, Adam D, Alnemri E S, Altucci L, Andrews D, Annicchiarico-Petruzzelli M, Baehrecke E H, Bazan N G, Bertrand M J, Bianchi K, Blagosklonny M V, Blomgren K, Borner C, Bredesen D E, Brenner C, Campanella M, Candi E, Cecconi F, Chan F K, Chandel N S, Cheng E H, Chipuk J E, Cidlowski J A, Ciechanover A, Dawson T M, Dawson V L, De Laurenzi V, De Maria R, Debatin K-M, Di Daniele N, Dixit V M, Dynlacht B D, El-Deiry W S, Fimia G M, Flavell R A, Fulda S, Garrido C, Gougeon M-L, Green D R, Gronemeyer H, Hajnoczky G, Hardwick J M, Hengartner M O, Ichijo H, Joseph B, Jost P J, Kaufmann T, Kepp O, Klionsky D J, Knight R A, Kumar S, Lemasters J J, Levine B, Linkermann A, Lipton S A, Lockshin R A, López-Otín C, Lugli E, Madeo F, Malorni W, Marine J-C, Martin S J, Martinou J-C, Medema J P, Meier P, Melino S, Mizushima N, Moll U, Muñoz-Pinedo C, Nuñez G, Oberst A, Panaretakis T, Penninger J M, Peter M E, Piacentini M, Pinton P, Prehn J H, Puthalakath H, Rabinovich G A, Ravichandran K S, Rizzuto R, Rodrigues C M, Rubinsztein D C, Rudel T, Shi Y, Simon H-U, Stockwell B R, Szabadkai G, Tait S W, Tang H L, Tavernarakis N, Tsujimoto Y, Vanden Berghe T, Vandenabeele P, Villunger A, Wagner E F, Walczak H, White E, Wood W G, Yuan J, Zakeri Z, Zhivotovsky B, Melino G, Kroemer G, Essential versus accessory aspects of cell death: recommendations of the NCCD 2015, 10.1038/cdd.2014.137
  98. Melcher Alan, Todryk Stephen, Hardwick Nicola, Ford Martin, Jacobson Michael, Vile Richard G., Tumor immunogenicity is determined by the mechanism of cell death via induction of heat shock protein expression, 10.1038/nm0598-581
  99. Gough M J, Melcher A A, Crittenden M R, Sanchez-Perez L, Voellmy R, Vile R G, Induction of cell stress through gene transfer of an engineered heat shock transcription factor enhances tumor immunogenicity, 10.1038/sj.gt.3302274
  100. Spisek R., Charalambous A., Mazumder A., Vesole D. H., Jagannath S., Dhodapkar M. V., 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, 10.1182/blood-2006-10-054221
  101. Casares Noelia, Pequignot Marie O., Tesniere Antoine, Ghiringhelli François, Roux Stéphan, Chaput Nathalie, Schmitt Elise, Hamai Ahmed, Hervas-Stubbs Sandra, Obeid Michel, Coutant Frédéric, Métivier Didier, Pichard Evelyne, Aucouturier Pierre, Pierron Gérard, Garrido Carmen, Zitvogel Laurence, Kroemer Guido, Caspase-dependent immunogenicity of doxorubicin-induced tumor cell death, 10.1084/jem.20050915
  102. Kroemer Guido, Galluzzi Lorenzo, Kepp Oliver, Zitvogel Laurence, Immunogenic Cell Death in Cancer Therapy, 10.1146/annurev-immunol-032712-100008
  103. Garg Abhishek D., Dudek-Peric Aleksandra M., Romano Erminia, Agostinis Patrizia, Immunogenic cell death, 10.1387/ijdb.150061pa
  104. Kepp Oliver, Senovilla Laura, Vitale Ilio, Vacchelli Erika, Adjemian Sandy, Agostinis Patrizia, Apetoh Lionel, Aranda Fernando, Barnaba Vincenzo, Bloy Norma, Bracci Laura, Breckpot Karine, Brough David, Buqué Aitziber, Castro Maria G., Cirone Mara, Colombo Maria I., Cremer Isabelle, Demaria Sandra, Dini Luciana, Eliopoulos Aristides G., Faggioni Alberto, Formenti Silvia C., Fučíková Jitka, Gabriele Lucia, Gaipl Udo S., Galon Jérôme, Garg Abhishek, Ghiringhelli François, Giese Nathalia A., Guo Zong Sheng, Hemminki Akseli, Herrmann Martin, Hodge James W., Holdenrieder Stefan, Honeychurch Jamie, Hu Hong-Min, Huang Xing, Illidge Tim M., Kono Koji, Korbelik Mladen, Krysko Dmitri V., Loi Sherene, Lowenstein Pedro R., Lugli Enrico, Ma Yuting, Madeo Frank, Manfredi Angelo A., Martins Isabelle, Mavilio Domenico, Menger Laurie, Merendino Nicolò, Michaud Michael, Mignot Gregoire, Mossman Karen L., Multhoff Gabriele, Oehler Rudolf, Palombo Fabio, Panaretakis Theocharis, Pol Jonathan, Proietti Enrico, Ricci Jean-Ehrland, Riganti Chiara, Rovere-Querini Patrizia, Rubartelli Anna, Sistigu Antonella, Smyth Mark J., Sonnemann Juergen, Spisek Radek, Stagg John, Sukkurwala Abdul Qader, Tartour Eric, Thorburn Andrew, Thorne Stephen H., Vandenabeele Peter, Velotti Francesca, Workenhe Samuel T., Yang Haining, Zong Wei-Xing, Zitvogel Laurence, Kroemer Guido, Galluzzi Lorenzo, Consensus guidelines for the detection of immunogenic cell death, 10.4161/21624011.2014.955691
  105. Dudek Aleksandra M., Martin Shaun, Garg Abhishek D., Agostinis Patrizia, Immature, Semi-Mature, and Fully Mature Dendritic Cells: Toward a DC-Cancer Cells Interface That Augments Anticancer Immunity, 10.3389/fimmu.2013.00438
  106. Ma Yuting, Adjemian Sandy, Mattarollo Stephen R., Yamazaki Takahiro, Aymeric Laetitia, Yang Heng, Portela Catani João Paulo, Hannani Dalil, Duret Helene, Steegh Kim, Martins Isabelle, Schlemmer Frederic, Michaud Mickaël, Kepp Oliver, Sukkurwala Abdul Qader, Menger Laurie, Vacchelli Erika, Droin Nathalie, Galluzzi Lorenzo, Krzysiek Roman, Gordon Siamon, Taylor Philip R., Van Endert Peter, Solary Eric, Smyth Mark J., Zitvogel Laurence, Kroemer Guido, Anticancer Chemotherapy-Induced Intratumoral Recruitment and Differentiation of Antigen-Presenting Cells, 10.1016/j.immuni.2013.03.003
  107. Zhang Jian-Guo, Czabotar Peter E., Policheni Antonia N., Caminschi Irina, San Wan Soo, Kitsoulis Susie, Tullett Kirsteen M., Robin Adeline Y., Brammananth Rajini, van Delft Mark F., Lu Jinhua, O'Reilly Lorraine A., Josefsson Emma C., Kile Benjamin T., Chin Wei Jin, Mintern Justine D., Olshina Maya A., Wong Wilson, Baum Jake, Wright Mark D., Huang David C.S., Mohandas Narla, Coppel Ross L., Colman Peter M., Nicola Nicos A., Shortman Ken, Lahoud Mireille H., The Dendritic Cell Receptor Clec9A Binds Damaged Cells via Exposed Actin Filaments, 10.1016/j.immuni.2012.03.009
  108. Garnett Charlie T., Palena Claudia, Chakarborty Mala, Tsang Kwong-Yok, Schlom Jeffrey, Hodge James W., Sublethal Irradiation of Human Tumor Cells Modulates Phenotype Resulting in Enhanced Killing by Cytotoxic T Lymphocytes, 10.1158/0008-5472.can-04-1525
  109. Hodge James W., Garnett Charlie T., Farsaci Benedetto, Palena Claudia, Tsang Kwong-Yok, Ferrone Soldano, Gameiro Sofia R., Chemotherapy-induced immunogenic modulation of tumor cells enhances killing by cytotoxic T lymphocytes and is distinct from immunogenic cell death : Chemotherapy induces immunogenic modulation, 10.1002/ijc.28070
  110. Gameiro Sofia R., Jammeh Momodou L., Wattenberg Max M., Tsang Kwong Y., Ferrone Soldano, Hodge James W., Radiation-induced immunogenic modulation of tumor enhances antigen processing and calreticulin exposure, resulting in enhanced T-cell killing, 10.18632/oncotarget.1719
  111. Michaud M., Martins I., Sukkurwala A. Q., Adjemian S., Ma Y., Pellegatti P., Shen S., Kepp O., Scoazec M., Mignot G., Rello-Varona S., Tailler M., Menger L., Vacchelli E., Galluzzi L., Ghiringhelli F., di Virgilio F., Zitvogel L., Kroemer G., Autophagy-Dependent Anticancer Immune Responses Induced by Chemotherapeutic Agents in Mice, 10.1126/science.1208347
  112. Garg A D, Dudek A M, Agostinis P, Calreticulin surface exposure is abrogated in cells lacking, chaperone-mediated autophagy-essential gene, LAMP2A, 10.1038/cddis.2013.372
  113. Martins I, Wang Y, Michaud M, Ma Y, Sukkurwala A Q, Shen S, Kepp O, Métivier D, Galluzzi L, Perfettini J-L, Zitvogel L, Kroemer G, Molecular mechanisms of ATP secretion during immunogenic cell death, 10.1038/cdd.2013.75
  114. Kazama Hirotaka, Ricci Jean-Ehrland, Herndon John M., Hoppe George, Green Douglas R., Ferguson Thomas A., Induction of Immunological Tolerance by Apoptotic Cells Requires Caspase-Dependent Oxidation of High-Mobility Group Box-1 Protein, 10.1016/j.immuni.2008.05.013
  115. Jube S., Rivera Z. S., Bianchi M. E., Powers A., Wang E., Pagano I., Pass H. I., Gaudino G., Carbone M., Yang H., Cancer Cell Secretion of the DAMP Protein HMGB1 Supports Progression in Malignant Mesothelioma, 10.1158/0008-5472.can-11-3481
  116. Garg Abhishek D., Krysko Dmitri V., Vandenabeele Peter, Agostinis Patrizia, Hypericin-based photodynamic therapy induces surface exposure of damage-associated molecular patterns like HSP70 and calreticulin, 10.1007/s00262-011-1184-2
  117. Lancaster Graeme I., Febbraio Mark A., Exosome-dependent Trafficking of HSP70 : A NOVEL SECRETORY PATHWAY FOR CELLULAR STRESS PROTEINS, 10.1074/jbc.m502017200
  118. Mambula S. S., Calderwood S. K., Heat Shock Protein 70 Is Secreted from Tumor Cells by a Nonclassical Pathway Involving Lysosomal Endosomes, 10.4049/jimmunol.177.11.7849
  119. Vega V. L., Rodriguez-Silva M., Frey T., Gehrmann M., Diaz J. C., Steinem C., Multhoff G., Arispe N., De Maio A., Hsp70 Translocates into the Plasma Membrane after Stress and Is Released into the Extracellular Environment in a Membrane-Associated Form that Activates Macrophages, 10.4049/jimmunol.180.6.4299
  120. Kötter Bernhard, Frey Benjamin, Winderl Markus, Rubner Yvonne, Scheithauer Heike, Sieber Renate, Fietkau Rainer, Gaipl Udo S., The in vitro immunogenic potential of caspase-3 proficient breast cancer cells with basal low immunogenicity is increased by hypofractionated irradiation, 10.1186/s13014-015-0506-5
  121. Multhoff Gabriele, Botzler Claus, Wiesnet Marion, Müller Eva, Meier Thomas, Wilmanns Wolfgang, Issels Rolf D., A stress-inducible 72-kDa heat-shock protein (HSP72) is expressed on the surface of human tumor cells, but not on normal cells, 10.1002/ijc.2910610222
  122. Gastpar Robert, Gehrmann Mathias, Bausero Maria A., Asea Alexzander, Gross Catharina, Schroeder Josef A., Multhoff Gabriele, Heat Shock Protein 70 Surface-Positive Tumor Exosomes Stimulate Migratory and Cytolytic Activity of Natural Killer Cells, 10.1158/0008-5472.can-04-3804
  123. Panaretakis Theocharis, Kepp Oliver, Brockmeier Ulf, Tesniere Antoine, Bjorklund Ann-Charlotte, Chapman Daniel C, Durchschlag Michael, Joza Nicholas, Pierron Gérard, van Endert Peter, Yuan Junying, Zitvogel Laurence, Madeo Frank, Williams David B, Kroemer Guido, Mechanisms of pre-apoptotic calreticulin exposure in immunogenic cell death, 10.1038/emboj.2009.1
  124. Madeo Frank, Durchschlag Michael, Kepp Oliver, Panaretakis Theocharis, Zitvogel Laurence, Fröhlich Kai-Uwe, Kroemer Guido, Phylogenetic conservation of the preapoptotic calreticulin exposure pathway from yeast to mammals, 10.4161/cc.8.4.7794
  125. Martin S., Dudek-Perić A.M., Maes H., Garg A.D., Gabrysiak M., Demirsoy S., Swinnen J.V., Agostinis P., Concurrent MEK and autophagy inhibition is required to restore cell death associated danger-signalling in Vemurafenib-resistant melanoma cells, 10.1016/j.bcp.2014.12.003
  126. Szklarczyk Damian, Franceschini Andrea, Wyder Stefan, Forslund Kristoffer, Heller Davide, Huerta-Cepas Jaime, Simonovic Milan, Roth Alexander, Santos Alberto, Tsafou Kalliopi P., Kuhn Michael, Bork Peer, Jensen Lars J., von Mering Christian, STRING v10: protein–protein interaction networks, integrated over the tree of life, 10.1093/nar/gku1003
  127. Dudek Aleksandra M., Garg Abhishek D., Krysko Dmitri V., De Ruysscher Dirk, Agostinis Patrizia, Inducers of immunogenic cancer cell death, 10.1016/j.cytogfr.2013.01.005
  128. Bezu Lucillia, Gomes-de-Silva Ligia C., Dewitte Heleen, Breckpot Karine, Fucikova Jitka, Spisek Radek, Galluzzi Lorenzo, Kepp Oliver, Kroemer Guido, Combinatorial Strategies for the Induction of Immunogenic Cell Death, 10.3389/fimmu.2015.00187
  129. Siurala Mikko, Bramante Simona, Vassilev Lotta, Hirvinen Mari, Parviainen Suvi, Tähtinen Siri, Guse Kilian, Cerullo Vincenzo, Kanerva Anna, Kipar Anja, Vähä-Koskela Markus, Hemminki Akseli, Oncolytic adenovirus and doxorubicin-based chemotherapy results in synergistic antitumor activity against soft-tissue sarcoma : Oncolytic adenovirus and doxorubicin-based chemotherapy, 10.1002/ijc.29048
  130. Menger L., Vacchelli E., Adjemian S., Martins I., Ma Y., Shen S., Yamazaki T., Sukkurwala A. Q., Michaud M., Mignot G., Schlemmer F., Sulpice E., Locher C., Gidrol X., Ghiringhelli F., Modjtahedi N., Galluzzi L., Andre F., Zitvogel L., Kepp O., Kroemer G., Cardiac Glycosides Exert Anticancer Effects by Inducing Immunogenic Cell Death, 10.1126/scitranslmed.3003807
  131. Panaretakis T, Joza N, Modjtahedi N, Tesniere A, Vitale I, Durchschlag M, Fimia G M, Kepp O, Piacentini M, Froehlich K-U, van Endert P, Zitvogel L, Madeo F, Kroemer G, The co-translocation of ERp57 and calreticulin determines the immunogenicity of cell death, 10.1038/cdd.2008.67
  132. Tufi R, Panaretakis T, Bianchi K, Criollo A, Fazi B, Di Sano F, Tesniere A, Kepp O, Paterlini-Brechot P, Zitvogel L, Piacentini M, Szabadkai G, Kroemer G, Reduction of endoplasmic reticulum Ca2+ levels favors plasma membrane surface exposure of calreticulin, 10.1038/sj.cdd.4402275
  133. Martins I, Kepp O, Schlemmer F, Adjemian S, Tailler M, Shen S, Michaud M, Menger L, Gdoura A, Tajeddine N, Tesniere A, Zitvogel L, Kroemer G, Restoration of the immunogenicity of cisplatin-induced cancer cell death by endoplasmic reticulum stress, 10.1038/onc.2010.500
  134. Verfaillie T, Rubio N, Garg A D, Bultynck G, Rizzuto R, Decuypere J-P, Piette J, Linehan C, Gupta S, Samali A, Agostinis P, PERK is required at the ER-mitochondrial contact sites to convey apoptosis after ROS-based ER stress, 10.1038/cdd.2012.74
  135. Galluzzi Lorenzo, Bravo-San Pedro José Manuel, Kroemer Guido, Organelle-specific initiation of cell death, 10.1038/ncb3005
  136. Chaurio Ricardo A., Muñoz Luis E., Maueröder Christian, Janko Christina, Harrer Thomas, Fürnrohr Barbara G., Niederweis Michael, Bilyy Rostyslav, Schett Georg, Herrmann Martin, Berens Christian, The Progression of Cell Death Affects the Rejection of Allogeneic Tumors in Immune-Competent Mice – Implications for Cancer Therapy, 10.3389/fimmu.2014.00560
  137. Garg Abhishek D, Maes Hannelore, van Vliet Alexander R, Agostinis Patrizia, Targeting the hallmarks of cancer with therapy-induced endoplasmic reticulum (ER) stress, 10.4161/23723556.2014.975089
  138. van Vliet A.R., Martin S., Garg A.D., Agostinis P., The PERKs of damage-associated molecular patterns mediating cancer immunogenicity: From sensor to the plasma membrane and beyond, 10.1016/j.semcancer.2015.03.010
  139. Sukkurwala Abdul Qader, Adjemian Sandy, Senovilla Laura, Michaud Mickaël, Spaggiari Sabrina, Vacchelli Erika, Baracco Elisa Elena, Galluzzi Lorenzo, Zitvogel Laurence, Kepp Oliver, Kroemer Guido, Screening of novel immunogenic cell death inducers within the NCI Mechanistic Diversity Set, 10.4161/onci.28473
  140. Wong Daniel Yuan Qiang, Ong Wendy Wei Fang, Ang Wee Han, Induction of Immunogenic Cell Death by Chemotherapeutic Platinum Complexes, 10.1002/anie.201500934
  141. Sistigu Antonella, Yamazaki Takahiro, Vacchelli Erika, Chaba Kariman, Enot David P, Adam Julien, Vitale Ilio, Goubar Aicha, Baracco Elisa E, Remédios Catarina, Fend Laetitia, Hannani Dalil, Aymeric Laetitia, Ma Yuting, Niso-Santano Mireia, Kepp Oliver, Schultze Joachim L, Tüting 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, Préville Xavier, Uzè Gilles, Schreiber Robert D, Chow Melvyn T, Smyth Mark J, Proietti Enrico, André Fabrice, Kroemer Guido, Zitvogel Laurence, Cancer cell–autonomous contribution of type I interferon signaling to the efficacy of chemotherapy, 10.1038/nm.3708
  142. Ramakrishnan Rupal, Gabrilovich Dmitry I., The role of mannose-6-phosphate receptor and autophagy in influencing the outcome of combination therapy, 10.4161/auto.23485
  143. Kaminski Joseph M., Shinohara Eric, Summers James Bradley, Niermann Kenneth J., Morimoto Allan, Brousal Jeffrey, The controversial abscopal effect, 10.1016/j.ctrv.2005.03.004
  144. Golden Encouse B, Frances Derek, Pellicciotta Ilenia, Demaria Sandra, Helen Barcellos-Hoff Mary, Formenti Silvia C, Radiation fosters dose-dependent and chemotherapy-induced immunogenic cell death, 10.4161/onci.28518
  145. Garrido Greta, Rabasa Ailem, Sánchez Belinda, López María Victoria, Blanco Rances, López Armando, Hernández Diana Rosa, Pérez Rolando, Fernández Luis Enrique, Induction of Immunogenic Apoptosis by Blockade of Epidermal Growth Factor Receptor Activation with a Specific Antibody, 10.4049/jimmunol.1003477
  146. Bugaut Hélène, Bruchard Mélanie, Berger Hélène, Derangère Valentin, Odoul Ludivine, Euvrard Romain, Ladoire Sylvain, Chalmin Fanny, Végran Frédérique, Rébé Cédric, Apetoh Lionel, Ghiringhelli François, Mignot Grégoire, Bleomycin Exerts Ambivalent Antitumor Immune Effect by Triggering Both Immunogenic Cell Death and Proliferation of Regulatory T Cells, 10.1371/journal.pone.0065181
  147. Diaconu I., Cerullo V., Hirvinen M. L. M., Escutenaire S., Ugolini M., Pesonen S. K., Bramante S., Parviainen S., Kanerva A., Loskog A. S. I., Eliopoulos A. G., Pesonen S., Hemminki A., Immune Response Is an Important Aspect of the Antitumor Effect Produced by a CD40L-Encoding Oncolytic Adenovirus, 10.1158/0008-5472.can-11-2975
  148. Hemminki Otto, Parviainen Suvi, Juhila Juuso, Turkki Riku, Linder Nina, Lundin Johan, Kankainen Matti, Ristimäki Ari, Koski Anniina, Liikanen Ilkka, Oksanen Minna, Nettelbeck Dirk M., Kairemo Kalevi, Partanen Kaarina, Joensuu Timo, Kanerva Anna, Hemminki Akseli, Immunological data from cancer patients treated with Ad5/3 E2F Δ24 GMCSF suggests utility for tumor immunotherapy, 10.18632/oncotarget.2901
  149. Sun Chunli, Wang Haiying, Mao Shuang, Liu Ji, Li Shan, Wang Jufang, Reactive oxygen species involved in CT26 immunogenic cell death induced by Clostridium difficile toxin B, 10.1016/j.imlet.2015.02.007
  150. Miyamoto S., Inoue H., Nakamura T., Yamada M., Sakamoto C., Urata Y., Okazaki T., Marumoto T., Takahashi A., Takayama K., Nakanishi Y., Shimizu H., Tani K., Coxsackievirus B3 Is an Oncolytic Virus with Immunostimulatory Properties That Is Active against Lung Adenocarcinoma, 10.1158/0008-5472.can-11-3185
  151. Vacchelli Erika, Eggermont Alexander, Galon Jérôme, Sautès-Fridman Catherine, Zitvogel Laurence, Kroemer Guido, Galluzzi Lorenzo, Trial watch : Monoclonal antibodies in cancer therapy, 10.4161/onci.22789
  152. Schiavoni G., Sistigu A., Valentini M., Mattei F., Sestili P., Spadaro F., Sanchez M., Lorenzi S., D'Urso M. T., Belardelli F., Gabriele L., Proietti E., Bracci L., Cyclophosphamide Synergizes with Type I Interferons through Systemic Dendritic Cell Reactivation and Induction of Immunogenic Tumor Apoptosis, 10.1158/0008-5472.can-10-2788
  153. Viaud S., Saccheri F., Mignot G., Yamazaki T., Daillere R., Hannani D., Enot D. P., Pfirschke C., Engblom C., Pittet M. J., Schlitzer A., Ginhoux F., Apetoh L., Chachaty E., Woerther P.-L., Eberl G., Berard M., Ecobichon C., Clermont D., Bizet C., Gaboriau-Routhiau V., Cerf-Bensussan N., Opolon P., Yessaad N., Vivier E., Ryffel B., Elson C. O., Dore J., Kroemer G., Lepage P., Boneca I. G., Ghiringhelli F., Zitvogel L., The Intestinal Microbiota Modulates the Anticancer Immune Effects of Cyclophosphamide, 10.1126/science.1240537
  154. Fucikova Jitka, Moserova Irena, Truxova Iva, Hermanova Ivana, Vancurova Irena, Partlova Simona, Fialova Anna, Sojka Ludek, Cartron Pierre-Francois, Houska Milan, Rob Lukas, Bartunkova Jirina, Spisek Radek, High hydrostatic pressure induces immunogenic cell death in human tumor cells : Effect of HHP in human tumor cells, 10.1002/ijc.28766
  155. Adkins Irena, Fucikova Jitka, Garg Abhishek D, Agostinis Patrizia, Špíšek Radek, Physical modalities inducing immunogenic tumor cell death for cancer immunotherapy, 10.4161/21624011.2014.968434
  156. Weiss E. M., Meister S., Janko C., Ebel N., Schlücker E., Meyer-Pittroff R., Fietkau R., Herrmann M., Gaipl U. S., Frey B., High hydrostatic pressure treatment generates inactivated mammalian tumor cells with immunogeneic features, 10.3109/15476911003657414
  157. Garg Abhishek D., Agostinis Patrizia, ER stress, autophagy and immunogenic cell death in photodynamic therapy-induced anti-cancer immune responses, 10.1039/c3pp50333j
  158. Yu Zhe, Geng Jie, Zhang Minghua, Zhou Yong, Fan Qingyu, Chen Jingyuan, Treatment of osteosarcoma with microwave thermal ablation to induce immunogenic cell death, 10.18632/oncotarget.2310
  159. Zamarin D., Holmgaard R. B., Subudhi S. K., Park J. S., Mansour M., Palese P., Merghoub T., Wolchok J. D., Allison J. P., Localized Oncolytic Virotherapy Overcomes Systemic Tumor Resistance to Immune Checkpoint Blockade Immunotherapy, 10.1126/scitranslmed.3008095
  160. Chen Hui-Ming, Wang Pi-Hsueh, Chen Swey-Shen, Wen Chih-Chun, Chen Yun-Hsiang, Yang Wen-Chin, Yang Ning-Sun, Shikonin induces immunogenic cell death in tumor cells and enhances dendritic cell-based cancer vaccine, 10.1007/s00262-012-1258-9
  161. Korbelik, Cancer Res, 59, 1941 (1999)
  162. Krosl G, Korbelik M, Dougherty GJ, Induction of immune cell infiltration into murine SCCVII tumour by photofrin-based photodynamic therapy, 10.1038/bjc.1995.108
  163. Korbelik M, Stott B, Sun J, Photodynamic therapy-generated vaccines: relevance of tumour cell death expression, 10.1038/sj.bjc.6604059
  164. Korbelik Mladen, Zhang Wei, Merchant Soroush, Involvement of damage-associated molecular patterns in tumor response to photodynamic therapy: surface expression of calreticulin and high-mobility group box-1 release, 10.1007/s00262-011-1047-x
  165. Duewell P, Steger A, Lohr H, Bourhis H, Hoelz H, Kirchleitner S V, Stieg M R, Grassmann S, Kobold S, Siveke J T, Endres S, Schnurr M, RIG-I-like helicases induce immunogenic cell death of pancreatic cancer cells and sensitize tumors toward killing by CD8+ T cells, 10.1038/cdd.2014.96
  166. West A. C., Mattarollo S. R., Shortt J., Cluse L. A., Christiansen A. J., Smyth M. J., Johnstone R. W., An Intact Immune System Is Required for the Anticancer Activities of Histone Deacetylase Inhibitors, 10.1158/0008-5472.can-13-0890
  167. Yang Yong, Li Xian-Jing, Chen Zhen, Zhu Xuan-Xuan, Wang Jing, Zhang Lin-bo, Qiang Lei, Ma Yan-jun, Li Zhi-yu, Guo Qing-Long, You Qi-Dong, Wogonin Induced Calreticulin/Annexin A1 Exposure Dictates the Immunogenicity of Cancer Cells in a PERK/AKT Dependent Manner, 10.1371/journal.pone.0050811
  168. Panzarini Elisa, Inguscio Valentina, Fimia Gian Maria, Dini Luciana, Rose Bengal Acetate PhotoDynamic Therapy (RBAc-PDT) Induces Exposure and Release of Damage-Associated Molecular Patterns (DAMPs) in Human HeLa Cells, 10.1371/journal.pone.0105778
  169. Molinari Romina, D’Eliseo Donatella, Manzi Laura, Zolla Lello, Velotti Francesca, Merendino Nicolò, The n3-polyunsaturated fatty acid docosahexaenoic acid induces immunogenic cell death in human cancer cell lines via pre-apoptotic calreticulin exposure, 10.1007/s00262-011-1074-7
  170. D’Eliseo Donatella, Manzi Laura, Velotti Francesca, Capsaicin as an inducer of damage-associated molecular patterns (DAMPs) of immunogenic cell death (ICD) in human bladder cancer cells, 10.1007/s12192-013-0422-2
  171. Gilardini Montani Maria Saveria, D’Eliseo Donatella, Cirone Mara, Di Renzo Livia, Faggioni Alberto, Santoni Angela, Velotti Francesca, Capsaicin-mediated apoptosis of human bladder cancer cells activates dendritic cells via CD91, 10.1016/j.nut.2014.05.005
  172. Janeway, Immunobiology: The Immune System in Health and Disease, 823 (2005)
  173. Fucikova J., Kralikova P., Fialova A., Brtnicky T., Rob L., Bartunkova J., Spisek R., Human Tumor Cells Killed by Anthracyclines Induce a Tumor-Specific Immune Response, 10.1158/0008-5472.can-11-0950
  174. Krysko D V, Kaczmarek A, Krysko O, Heyndrickx L, Woznicki J, Bogaert P, Cauwels A, Takahashi N, Magez S, Bachert C, Vandenabeele P, TLR-2 and TLR-9 are sensors of apoptosis in a mouse model of doxorubicin-induced acute inflammation, 10.1038/cdd.2011.4
  175. Tseng Ling-Ming, Liu Chun-Yu, Chang Kung-Chi, Chu Pei-Yi, Shiau Chung-Wai, Chen Kuen-Feng, CIP2A is a target of bortezomib in human triple negative breast cancer cells, 10.1186/bcr3175
  176. Davies A. M., Lara P. N., Mack P. C., Gandara D. R., Incorporating Bortezomib into the Treatment of Lung Cancer, 10.1158/1078-0432.ccr-07-0334
  177. Huang Tuxiong, Li Shan, Li Guangchao, Tian Yuan, Wang Haiying, Shi Lianfa, Perez-Cordon Gregorio, Mao Li, Wang Xiaoning, Wang Jufang, Feng Hanping, Utility of Clostridium difficile Toxin B for Inducing Anti-Tumor Immunity, 10.1371/journal.pone.0110826
  178. Bravim Fernanda, De Freitas Jéssica M., Fernandes A. Alberto R., Fernandes Patricia M. B., High hydrostatic pressure and the cell membrane : Stress response of Saccharomyces cerevisiae, 10.1111/j.1749-6632.2009.05182.x
  179. Senovilla L., Vitale I., Martins I., Tailler M., Pailleret C., Michaud M., Galluzzi L., Adjemian S., Kepp O., Niso-Santano M., Shen S., Marino G., Criollo A., Boileve A., Job B., Ladoire S., Ghiringhelli F., Sistigu A., Yamazaki T., Rello-Varona S., Locher C., Poirier-Colame V., Talbot M., Valent A., Berardinelli F., Antoccia A., Ciccosanti F., Fimia G. M., Piacentini M., Fueyo A., Messina N. L., Li M., Chan C. J., Sigl V., Pourcher G., Ruckenstuhl C., Carmona-Gutierrez D., Lazar V., Penninger J. M., Madeo F., Lopez-Otin C., Smyth M. J., Zitvogel L., Castedo M., Kroemer G., An Immunosurveillance Mechanism Controls Cancer Cell Ploidy, 10.1126/science.1224922
  180. Korbelik Mladen, Cancer vaccines generated by photodynamic therapy, 10.1039/c0pp00343c
  181. Garg Abhishek D., Krysko Dmitri V., Vandenabeele Peter, Agostinis Patrizia, DAMPs and PDT-mediated photo-oxidative stress: exploring the unknown, 10.1039/c0pp00294a
  182. Chen J, Xie J, Jiang Z, Wang B, Wang Y, Hu X, Shikonin and its analogs inhibit cancer cell glycolysis by targeting tumor pyruvate kinase-M2, 10.1038/onc.2011.137
  183. Tsai Cheng-Fang, Yeh Wei-Lan, Huang Ssu Ming, Tan Tzu-Wei, Lu Dah-Yuu, Wogonin Induces Reactive Oxygen Species Production and Cell Apoptosis in Human Glioma Cancer Cells, 10.3390/ijms13089877
  184. Sanovic Renata, Verwanger Thomas, Hartl Arnulf, Krammer Barbara, Low dose hypericin-PDT induces complete tumor regression in BALB/c mice bearing CT26 colon carcinoma, 10.1016/j.pdpdt.2011.04.003
  185. Garg Abhishek D., Krysko Dmitri V., Vandenabeele Peter, Agostinis Patrizia, The emergence of phox-ER stress induced immunogenic apoptosis, 10.4161/onci.19750
  186. Liu Zhen, Zhang Huifang M., Yuan Ji, Ye Xin, Taylor Gregory A., Yang Decheng, The immunity-related GTPase Irgm3 relieves endoplasmic reticulum stress response during coxsackievirus B3 infection via a PI3K/Akt dependent pathway : Irgm3 relieves CVB3-induced ER stress response, 10.1111/j.1462-5822.2011.01708.x
  187. Bian Jianchun, Wang Kai, Kong Xiangang, Liu Huairan, Chen Fei, Hu Maozhi, Zhang Xiaorong, Jiao Xinan, Ge Baoxue, Wu Yantao, Meng Songshu, Caspase- and p38-MAPK-dependent induction of apoptosis in A549 lung cancer cells by Newcastle disease virus, 10.1007/s00705-011-0987-y
  188. Garg Abhishek D., De Ruysscher Dirk, Agostinis Patrizia, Immunological metagene signatures derived from immunogenic cancer cell death associate with improved survival of patients with lung, breast or ovarian malignancies: A large-scale meta-analysis, 10.1080/2162402x.2015.1069938
  189. Galluzzi Lorenzo, Kepp Oliver, Kroemer Guido, Enlightening the impact of immunogenic cell death in photodynamic cancer therapy : Molecular cascades towards immunogenicity, 10.1038/emboj.2012.2
  190. Galluzzi L., Pietrocola F., Bravo-San Pedro J. M., Amaravadi R. K., Baehrecke E. H., Cecconi F., Codogno P., Debnath J., Gewirtz D. A., Karantza V., Kimmelman A., Kumar S., Levine B., Maiuri M. C., Martin S. J., Penninger J., Piacentini M., Rubinsztein D. C., Simon H.-U., Simonsen A., Thorburn A. M., Velasco G., Ryan K. M., Kroemer G., Autophagy in malignant transformation and cancer progression, 10.15252/embj.201490784
  191. Mattarollo S. R., Loi S., Duret H., Ma Y., Zitvogel L., Smyth M. J., Pivotal Role of Innate and Adaptive Immunity in Anthracycline Chemotherapy of Established Tumors, 10.1158/0008-5472.can-11-0753
  192. Lin Tien-Jen, Lin Hsin-Ting, Chang Wei-Ting, Mitapalli. S Pradeep, Hsiao Pei-Wen, Yin Shu-Yi, Yang Ning-Sun, Shikonin-enhanced cell immunogenicity of tumor vaccine is mediated by the differential effects of DAMP components, 10.1186/s12943-015-0435-9
  193. Ma Yuting, Aymeric Laetitia, Locher Clara, Mattarollo Stephen R., Delahaye Nicolas F., Pereira Pablo, Boucontet Laurent, Apetoh Lionel, Ghiringhelli François, Casares Noëlia, Lasarte Juan José, Matsuzaki Goro, Ikuta Koichi, Ryffel Bernard, Benlagha Kamel, Tesnière Antoine, Ibrahim Nicolas, Déchanet-Merville Julie, Chaput Nathalie, Smyth Mark J., Kroemer Guido, Zitvogel Laurence, Contribution of IL-17–producing γδ T cells to the efficacy of anticancer chemotherapy, 10.1084/jem.20100269
  194. Yang Heng, Yamazaki Takahiro, Pietrocola Federico, Zhou Heng, Zitvogel Laurence, Ma Yuting, Kroemer Guido, STAT3 Inhibition Enhances the Therapeutic Efficacy of Immunogenic Chemotherapy by Stimulating Type 1 Interferon Production by Cancer Cells, 10.1158/0008-5472.can-15-1122
  195. Ciampricotti Metamia, Hau Cheei-Sing, Doornebal Chris W, Jonkers Jos, de Visser Karin E, Chemotherapy response of spontaneous mammary tumors is independent of the adaptive immune system, 10.1038/nm.2652
  196. Gould Stephen E, Junttila Melissa R, de Sauvage Frederic J, Translational value of mouse models in oncology drug development, 10.1038/nm.3853
  197. Tesniere A, Schlemmer F, Boige V, Kepp O, Martins I, Ghiringhelli F, Aymeric L, Michaud M, Apetoh L, Barault L, Mendiboure J, Pignon J-P, Jooste V, van Endert P, Ducreux M, Zitvogel L, Piard F, Kroemer G, Immunogenic death of colon cancer cells treated with oxaliplatin, 10.1038/onc.2009.356
  198. Hannesdóttir Lára, Tymoszuk Piotr, Parajuli Nirmala, Wasmer Marie-Helene, Philipp Sonja, Daschil Nina, Datta Sebak, Koller Johann-Benedikt, Tripp Christoph H., Stoitzner Patrizia, Müller-Holzner Elisabeth, Wiegers Gerrit Jan, Sexl Veronika, Villunger Andreas, Doppler Wolfgang, Lapatinib and doxorubicin enhance the Stat1-dependent antitumor immune response : Immunomodulation, 10.1002/eji.201242505
  199. Michaud Mickaël, Xie Xiaoqi, Bravo-San Pedro José Manuel, Zitvogel Laurence, White Eileen, Kroemer Guido, An autophagy-dependent anticancer immune response determines the efficacy of melanoma chemotherapy, 10.4161/21624011.2014.944047
  200. Demaria Sandra, Santori Fabio R., Ng Bruce, Liebes Leonard, Formenti Silvia C., Vukmanovic Stanislav, Select forms of tumor cell apoptosis induce dendritic cell maturation, 10.1189/jlb.0804478
  201. Schumacher L. Y., Vo D. D., Garban H. J., Comin-Anduix B., Owens S. K., Dissette V. B., Glaspy J. A., McBride W. H., Bonavida B., Economou J. S., Ribas A., Immunosensitization of Tumor Cells to Dendritic Cell-Activated Immune Responses with the Proteasome Inhibitor Bortezomib (PS-341, Velcade), 10.4049/jimmunol.176.8.4757
  202. Chang C.-L., Hsu Y.-T., Wu C.-C., Yang Y.-C., Wang C., Wu T.- C., Hung C.-F., Immune Mechanism of the Antitumor Effects Generated by Bortezomib, 10.4049/jimmunol.1103826
  203. van der Most Robbert G., Currie Andrew J., Mahendran Sathish, Prosser Amy, Darabi Anna, Robinson Bruce W. S., Nowak Anna K., Lake Richard A., Tumor eradication after cyclophosphamide depends on concurrent depletion of regulatory T cells: a role for cycling TNFR2-expressing effector-suppressor T cells in limiting effective chemotherapy, 10.1007/s00262-008-0628-9
  204. Obeid M, Panaretakis T, Joza N, Tufi R, Tesniere A, van Endert P, Zitvogel L, Kroemer G, Calreticulin exposure is required for the immunogenicity of γ-irradiation and UVC light-induced apoptosis, 10.1038/sj.cdd.4402201
  205. Carr-Brendel Victoria, Markovic Dubravka, Smith Michael, Taylor-Papadimitriou Joyce, Cohen Edward P., Immunity to Breast Cancer in Mice Immunized with X-Irradiated Breast Cancer Cells Modified to Secrete IL-12 : , 10.1097/00002371-199909000-00005
  206. Strome, Cancer Res, 62, 1884 (2002)
  207. Prasad S. J., Farrand K. J., Matthews S. A., Chang J. H., McHugh R. S., Ronchese F., Dendritic Cells Loaded with Stressed Tumor Cells Elicit Long-Lasting Protective Tumor Immunity in Mice Depleted of CD4+CD25+ Regulatory T Cells, 10.4049/jimmunol.174.1.90
  208. Yang Huanjie, Zhou Ping, Huang Hongbiao, Chen Di, Ma Ningfang, Cui Qiuzhi Cindy, Shen Shouxing, Dong Weihua, Zhang Xiaoyan, Lian Wen, Wang Xuejun, Dou Q. Ping, Liu Jinbao, Shikonin exerts antitumor activityviaproteasome inhibition and cell death inductionin vitroandin vivo, 10.1002/ijc.24195
  209. Sharma P., Allison J. P., The future of immune checkpoint therapy, 10.1126/science.aaa8172
  210. Viney M., Lazarou L., Abolins S., The laboratory mouse and wild immunology, 10.1111/pim.12150
  211. Davis Mark M., A Prescription for Human Immunology, 10.1016/j.immuni.2008.12.003
  212. Mestas J., Hughes C. C. W., Of Mice and Not Men: Differences between Mouse and Human Immunology, 10.4049/jimmunol.172.5.2731
  213. Tubiana M., The growth and progression of human tumors: Implications for management strategy, 10.1016/s0167-8140(86)80151-7
  214. Klein Christoph A., Parallel progression of primary tumours and metastases, 10.1038/nrc2627
  215. Yamazaki T, Hannani D, Poirier-Colame V, Ladoire S, Locher C, Sistigu A, Prada N, Adjemian S, Catani J PP, Freudenberg M, Galanos C, André F, Kroemer G, Zitvogel L, Defective immunogenic cell death of HMGB1-deficient tumors: compensatory therapy with TLR4 agonists, 10.1038/cdd.2013.72
  216. Loi S., Pommey S., Haibe-Kains B., Beavis P. A., Darcy P. K., Smyth M. J., Stagg J., CD73 promotes anthracycline resistance and poor prognosis in triple negative breast cancer, 10.1073/pnas.1222251110
  217. Shalapour Shabnam, Font-Burgada Joan, Di Caro Giuseppe, Zhong Zhenyu, Sanchez-Lopez Elsa, Dhar Debanjan, Willimsky Gerald, Ammirante Massimo, Strasner Amy, Hansel Donna E., Jamieson Christina, Kane Christopher J., Klatte Tobias, Birner Peter, Kenner Lukas, Karin Michael, Immunosuppressive plasma cells impede T-cell-dependent immunogenic chemotherapy, 10.1038/nature14395
  218. De Boo Sara, Kopecka Joanna, Brusa Davide, Gazzano Elena, Matera Lina, Ghigo Dario, Bosia Amalia, Riganti Chiara, iNOS activity is necessary for the cytotoxic and immunogenic effects of doxorubicin in human colon cancer cells, 10.1186/1476-4598-8-108
  219. Riganti Chiara, Castella Barbara, Kopecka Joanna, Campia Ivana, Coscia Marta, Pescarmona Gianpiero, Bosia Amalia, Ghigo Dario, Massaia Massimo, Zoledronic Acid Restores Doxorubicin Chemosensitivity and Immunogenic Cell Death in Multidrug-Resistant Human Cancer Cells, 10.1371/journal.pone.0060975
  220. Stoll Gautier, Enot David, Mlecnik Bernhard, Galon Jérôme, Zitvogel Laurence, Kroemer Guido, Immune-related gene signatures predict the outcome of neoadjuvant chemotherapy, 10.4161/onci.27884
  221. Pardoll Drew M., The blockade of immune checkpoints in cancer immunotherapy, 10.1038/nrc3239
  222. Galon Jérôme, Angell Helen K., Bedognetti Davide, Marincola Francesco M., The Continuum of Cancer Immunosurveillance: Prognostic, Predictive, and Mechanistic Signatures, 10.1016/j.immuni.2013.07.008
  223. Fridman Wolf Herman, Pagès Franck, Sautès-Fridman Catherine, Galon Jérôme, The immune contexture in human tumours: impact on clinical outcome, 10.1038/nrc3245
  224. Zitvogel Laurence, Tesniere Antoine, Kroemer Guido, Cancer despite immunosurveillance: immunoselection and immunosubversion, 10.1038/nri1936
  225. Ladoire Sylvain, Penault-Llorca Frédérique, Senovilla Laura, Dalban Cécile, Enot David, Locher Clara, Prada Nicole, Poirier-Colame Vichnou, Chaba Kariman, Arnould Laurent, Ghiringhelli François, Fumoleau Pierre, Spielmann Marc, Delaloge Suzette, Poillot Marie Laure, Arveux Patrick, Goubar Aicha, Andre Fabrice, Zitvogel Laurence, Kroemer Guido, Combined evaluation of LC3B puncta and HMGB1 expression predicts residual risk of relapse after adjuvant chemotherapy in breast cancer, 10.1080/15548627.2015.1082022
  226. Kacerovská Denisa, Pizinger Karel, Majer Filip, Šmíd František, Photodynamic Therapy of Nonmelanoma Skin Cancer with Topical Hypericum perforatum Extract—A Pilot Study, 10.1111/j.1751-1097.2007.00260.x
  227. Rook Alain H., Wood Gary S., Duvic Madeleine, Vonderheid Eric C., Tobia Alfonso, Cabana Bernard, A phase II placebo-controlled study of photodynamic therapy with topical hypericin and visible light irradiation in the treatment of cutaneous T-cell lymphoma and psoriasis, 10.1016/j.jaad.2010.02.039
  228. Koren H., Schenk G.M., Iindra R.H., Alth G., Ebermann R., Kubin A., Koderhold G., Kreitner M., Hypericin in phototherapy, 10.1016/s1011-1344(96)07357-5
  229. Alecu, Anticancer Res, 18, 4651 (1998)
  230. Liikanen Ilkka, Koski Anniina, Merisalo-Soikkeli Maiju, Hemminki Otto, Oksanen Minna, Kairemo Kalevi, Joensuu Timo, Kanerva Anna, Hemminki Akseli, Serum HMGB1 is a predictive and prognostic biomarker for oncolytic immunotherapy, 10.4161/2162402x.2014.989771
  231. Agostinis Patrizia, Berg Kristian, Cengel Keith A., Foster Thomas H., Girotti Albert W., Gollnick Sandra O., Hahn Stephen M., Hamblin Michael R., Juzeniene Asta, Kessel David, Korbelik Mladen, Moan Johan, Mroz Pawel, Nowis Dominika, Piette Jacques, Wilson Brian C., Golab Jakub, Photodynamic therapy of cancer: An update, 10.3322/caac.20114
  232. Suzuki Y., Mimura K., Yoshimoto Y., Watanabe M., Ohkubo Y., Izawa S., Murata K., Fujii H., Nakano T., Kono K., Immunogenic Tumor Cell Death Induced by Chemoradiotherapy in Patients with Esophageal Squamous Cell Carcinoma, 10.1158/0008-5472.can-12-0851
  233. Zappasodi R., Pupa S. M., Ghedini G. C., Bongarzone I., Magni M., Cabras A. D., Colombo M. P., Carlo-Stella C., Gianni A. M., Di Nicola M., Improved Clinical Outcome in Indolent B-Cell Lymphoma Patients Vaccinated with Autologous Tumor Cells Experiencing Immunogenic Death, 10.1158/0008-5472.can-10-1825
  234. Baitsch Lukas, Fuertes-Marraco Silvia A., Legat Amandine, Meyer Christiane, Speiser Daniel E., The three main stumbling blocks for anticancer T cells, 10.1016/j.it.2012.02.006
  235. Redmond William L., Sherman Linda A., Peripheral Tolerance of CD8 T Lymphocytes, 10.1016/j.immuni.2005.01.010
  236. Cole D. K., Pumphrey N. J., Boulter J. M., Sami M., Bell J. I., Gostick E., Price D. A., Gao G. F., Sewell A. K., Jakobsen B. K., Human TCR-Binding Affinity is Governed by MHC Class Restriction, 10.4049/jimmunol.178.9.5727
  237. Schmid D. A., Irving M. B., Posevitz V., Hebeisen M., Posevitz-Fejfar A., Sarria J. C. F., Gomez-Eerland R., Thome M., Schumacher T. N. M., Romero P., Speiser D. E., Zoete V., Michielin O., Rufer N., Evidence for a TCR Affinity Threshold Delimiting Maximal CD8 T Cell Function, 10.4049/jimmunol.1000173
  238. Zehn Dietmar, Bevan Michael J., T Cells with Low Avidity for a Tissue-Restricted Antigen Routinely Evade Central and Peripheral Tolerance and Cause Autoimmunity, 10.1016/j.immuni.2006.06.009
  239. Baumgaertner Petra, Jandus Camilla, Rivals Jean-Paul, Derré Laurent, Lövgren Tanja, Baitsch Lukas, Guillaume Philippe, Luescher Immanuel F., Berthod Gregoire, Matter Maurice, Rufer Nathalie, Michielin Olivier, Speiser Daniel E., Vaccination-induced functional competence of circulating human tumor-specific CD8 T-cells, 10.1002/ijc.26297
  240. Gubin Matthew M., Artyomov Maxim N., Mardis Elaine R., Schreiber Robert D., Tumor neoantigens: building a framework for personalized cancer immunotherapy, 10.1172/jci80008
  241. Schumacher T. N., Schreiber R. D., Neoantigens in cancer immunotherapy, 10.1126/science.aaa4971
  242. Twyman-Saint Victor Christina, Rech Andrew J., Maity Amit, Rengan Ramesh, Pauken Kristen E., Stelekati Erietta, Benci Joseph L., Xu Bihui, Dada Hannah, Odorizzi Pamela M., Herati Ramin S., Mansfield Kathleen D., Patsch Dana, Amaravadi Ravi K., Schuchter Lynn M., Ishwaran Hemant, Mick Rosemarie, Pryma Daniel A., Xu Xiaowei, Feldman Michael D., Gangadhar Tara C., Hahn Stephen M., Wherry E. John, Vonderheide Robert H., Minn Andy J., Radiation and dual checkpoint blockade activate non-redundant immune mechanisms in cancer, 10.1038/nature14292
  243. Ochsenbein A. F., Klenerman P., Karrer U., Ludewig B., Pericin M., Hengartner H., Zinkernagel R. M., Immune surveillance against a solid tumor fails because of immunological ignorance, 10.1073/pnas.96.5.2233
  244. Chu-Yuan Hong, Jing Peng, Yi-Sheng Wei, He-Ping Peng, Hui Yang, Chu-Xiong Zhao, Guo-Jian Liang, Guo-Qiang Wang, The impact of chemotherapy-associated neutrophil/ lymphocyte counts on prognosis of adjuvant chemotherapy in colorectal cancer, 10.1186/1471-2407-13-177
  245. Inogès Susana, Rodrìguez-Calvillo Mercedes, Zabalegui Natalia, Lòpez-Dìaz de Cerio Ascensiòn, Villanueva Helena, Soria Elena, Suárez Lilia, Rodríguez-Caballero Arancha, Pastor Fernando, García-Muñóz Ricardo, Panizo Carlos, Pèrez-Calvo Javier, Melero Ignacio, Rocha Eduardo, Orfao Alberto, Bendandi Maurizio, Clinical Benefit Associated With Idiotypic Vaccination in Patients With Follicular Lymphoma, 10.1093/jnci/djj358
  246. Kakarla Sunitha, Gottschalk Stephen, CAR T Cells for Solid Tumors : Armed and Ready to Go?, 10.1097/ppo.0000000000000032
Bibliographic reference Garg, Abhishek D ; Galluzzi, Lorenzo ; Apetoh, Lionel ; Baert, Thais ; Birge, Raymond B ; et. al. Molecular and Translational Classifications of DAMPs in Immunogenic Cell Death.. In: Frontiers in Immunology, Vol. 6, p. 588 (2015)
Permanent URL http://hdl.handle.net/2078.1/172396