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Trial Watch: Immunostimulation with recombinant cytokines for cancer therapy

E. García-Martínez, M. Smith, A. Buqué, F. Aranda, FA. de la Peña, A. Ivars, MS. Cánovas, MAV. Conesa, J. Fucikova, R. Spisek, L. Zitvogel, G. Kroemer, L. Galluzzi,

. 2018 ; 7 (6) : e1433982. [pub] 20180215

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/bmc18023991

Cytokines regulate virtually aspects of innate and adaptive immunity, including the initiation, execution and extinction of tumor-targeting immune responses. Over the past three decades, the possibility of using recombinant cytokines as a means to elicit or boost clinically relevant anticancer immune responses has attracted considerable attention. However, only three cytokines have been approved so far by the US Food and Drug Administration and the European Medicines Agency for use in cancer patients, namely, recombinant interleukin (IL)-2 and two variants of recombinant interferon alpha 2 (IFN-α2a and IFN-α2b). Moreover, the use of these cytokines in the clinics is steadily decreasing, mostly as a consequence of: (1) the elevated pleiotropism of IL-2, IFN-α2a and IFN-α2b, resulting in multiple unwarranted effects; and (2) the development of highly effective immunostimulatory therapeutics, such as immune checkpoint blockers. Despite this and other obstacles, research in the field continues as alternative cytokines with restricted effects on specific cell populations are being evaluated. Here, we summarize research preclinical and clinical developments on the use of recombinant cytokines for immunostimulation in cancer patients.

Citace poskytuje Crossref.org

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$a Cytokines regulate virtually aspects of innate and adaptive immunity, including the initiation, execution and extinction of tumor-targeting immune responses. Over the past three decades, the possibility of using recombinant cytokines as a means to elicit or boost clinically relevant anticancer immune responses has attracted considerable attention. However, only three cytokines have been approved so far by the US Food and Drug Administration and the European Medicines Agency for use in cancer patients, namely, recombinant interleukin (IL)-2 and two variants of recombinant interferon alpha 2 (IFN-α2a and IFN-α2b). Moreover, the use of these cytokines in the clinics is steadily decreasing, mostly as a consequence of: (1) the elevated pleiotropism of IL-2, IFN-α2a and IFN-α2b, resulting in multiple unwarranted effects; and (2) the development of highly effective immunostimulatory therapeutics, such as immune checkpoint blockers. Despite this and other obstacles, research in the field continues as alternative cytokines with restricted effects on specific cell populations are being evaluated. Here, we summarize research preclinical and clinical developments on the use of recombinant cytokines for immunostimulation in cancer patients.
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$a Buqué, Aitziber $u Department of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA.
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$a Aranda, Fernando $u Immunoreceptors of the Innate and Adaptive System, IDIBAPS, Barcelona, Spain.
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$a de la Peña, Francisco Ayala $u Hematology and Oncology Department, Hospital Universitario Morales Meseguer, Murcia, Spain.
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$a Ivars, Alejandra $u Hematology and Oncology Department, Hospital Universitario Morales Meseguer, Murcia, Spain.
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$a Cánovas, Manuel Sanchez $u Hematology and Oncology Department, Hospital Universitario Morales Meseguer, Murcia, Spain.
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$a Conesa, Ma Angeles Vicente $u Hematology and Oncology Department, Hospital Universitario Morales Meseguer, Murcia, Spain.
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$a Fucikova, Jitka $u Sotio, Prague, Czech Republic. Dept. of Immunology, 2nd Faculty of Medicine and University Hospital Motol, Charles University, Prague, Czech Republic.
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$a Spisek, Radek $u Sotio, Prague, Czech Republic. Dept. of Immunology, 2nd Faculty of Medicine and University Hospital Motol, Charles University, Prague, Czech Republic.
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$a Zitvogel, Laurence $u Gustave Roussy Comprehensive Cancer Institute, Villejuif, France. INSERM, U1015, Villejuif, France. Center of Clinical Investigations in Biotherapies of Cancer (CICBT) 1428, Villejuif, France. Université Paris Sud/Paris XI, Le Kremlin-Bicêtre, France.
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$a Kroemer, Guido $u Université Paris Descartes/Paris V, France. Université Pierre et Marie Curie/Paris VI, Paris. Equipe 11 labellisée Ligue contre le Cancer, Centre de Recherche des Cordeliers, Paris, France. INSERM, U1138, Paris, France. Metabolomics and Cell Biology Platforms, Gustave Roussy Comprehensive Cancer Institute, Villejuif, France. Karolinska Institute, Department of Women's and Children's Health, Karolinska University Hospital, Stockholm, Sweden. Pôle de Biologie, Hopitâl Européen George Pompidou, AP-HP, Paris, France.
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$a Galluzzi, Lorenzo $u Department of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA. Université Paris Descartes/Paris V, France. Sandra and Edward Meyer Cancer Center, New York, NY, USA.
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