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  5. Trial Watch: Immunostimulation with recombinant cytokines for cancer therapy

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Article
en
2018

Trial Watch: Immunostimulation with recombinant cytokines for cancer therapy

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0 Files

en
2018
Vol 7 (6)
Vol. 7
DOI: 10.1080/2162402x.2018.1433982

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Guido Guido Kroemer
Guido Guido Kroemer

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Elena García-Martínez
Melody Smith
Aitziber Buqué
+10 more

Abstract

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.

How to cite this publication

Elena García-Martínez, Melody Smith, Aitziber Buqué, Fernando Aranda, Francisco Ayala de la Peña, Alejandra Ivars, Manuel Sánchez Cánovas, M.A. Vicente Conesa, Jitka Fučíková, Radek Špíšek, Laurence Zitvogel, Guido Guido Kroemer, Lorenzo Galluzzi (2018). Trial Watch: Immunostimulation with recombinant cytokines for cancer therapy. , 7(6), DOI: https://doi.org/10.1080/2162402x.2018.1433982.

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Publication Details

Type

Article

Year

2018

Authors

13

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1080/2162402x.2018.1433982

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