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Interleukin-15 and cancer: some solved and many unsolved questions

Soluble interleukin (IL)-15 exists under two forms: as monomer (sIL-15) or as heterodimeric complex in association with sIL-15Rα (sIL-15/IL-15Rα). Both forms have been successfully tested in experimental tumor murine models and are currently undergoing investigation in phase I/II clinical trials. De...

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Autores principales: Fiore, Piera Filomena, Di Matteo, Sabina, Tumino, Nicola, Mariotti, Francesca Romana, Pietra, Gabriella, Ottonello, Selene, Negrini, Simone, Bottazzi, Barbara, Moretta, Lorenzo, Mortier, Erwan, Azzarone, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674108/
https://www.ncbi.nlm.nih.gov/pubmed/33203664
http://dx.doi.org/10.1136/jitc-2020-001428
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author Fiore, Piera Filomena
Di Matteo, Sabina
Tumino, Nicola
Mariotti, Francesca Romana
Pietra, Gabriella
Ottonello, Selene
Negrini, Simone
Bottazzi, Barbara
Moretta, Lorenzo
Mortier, Erwan
Azzarone, Bruno
author_facet Fiore, Piera Filomena
Di Matteo, Sabina
Tumino, Nicola
Mariotti, Francesca Romana
Pietra, Gabriella
Ottonello, Selene
Negrini, Simone
Bottazzi, Barbara
Moretta, Lorenzo
Mortier, Erwan
Azzarone, Bruno
author_sort Fiore, Piera Filomena
collection PubMed
description Soluble interleukin (IL)-15 exists under two forms: as monomer (sIL-15) or as heterodimeric complex in association with sIL-15Rα (sIL-15/IL-15Rα). Both forms have been successfully tested in experimental tumor murine models and are currently undergoing investigation in phase I/II clinical trials. Despite more than 20 years research on IL-15, some controversial issues remain to be addressed. A first point concerns the detection of the sIL-15/IL-15Rα in plasma of healthy donors or patients with cancer and its biological significance. The second and third unsolved question regards the protumorigenic role of the IL-15/IL-15Rα complex in human cancer and the detrimental immunological consequences associated to prolonged exposure of natural killer (NK) cells to both forms of soluble IL-15, respectively. Data suggest that in vivo prolonged or repeated exposure to monomeric sIL-15 or the soluble complex may lead to NK hypo-responsiveness through the expansion of the CD8(+)/CD44(+) T cell subset that would suppress NK cell functions. In vitro experiments indicate that soluble complex and monomeric IL-15 may cause NK hyporesponsiveness through a direct effect caused by their prolonged stimulation, suggesting that this mechanism could also be effective in vivo. Therefore, a better knowledge of IL-15 and a more appropriate use of both its soluble forms, in terms of concentrations and time of exposure, are essential in order to improve their therapeutic use. In cancer, the overproduction of sIL-15/IL-15Rα could represent a novel mechanism of immune escape. The soluble complex may act as a decoy cytokine unable to efficiently foster NK cells, or could induce NK hyporesponsiveness through an excessive and prolonged stimulation depending on the type of IL-15Rα isoforms associated. All these unsolved questions are not merely limited to the knowledge of IL-15 pathophysiology, but are crucial also for the therapeutic use of this cytokine. Therefore, in this review, we will discuss key unanswered issues on the heterogeneity and biological significance of IL-15 isoforms, analyzing both their cancer-related biological functions and their therapeutic implications.
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spelling pubmed-76741082020-11-30 Interleukin-15 and cancer: some solved and many unsolved questions Fiore, Piera Filomena Di Matteo, Sabina Tumino, Nicola Mariotti, Francesca Romana Pietra, Gabriella Ottonello, Selene Negrini, Simone Bottazzi, Barbara Moretta, Lorenzo Mortier, Erwan Azzarone, Bruno J Immunother Cancer Review Soluble interleukin (IL)-15 exists under two forms: as monomer (sIL-15) or as heterodimeric complex in association with sIL-15Rα (sIL-15/IL-15Rα). Both forms have been successfully tested in experimental tumor murine models and are currently undergoing investigation in phase I/II clinical trials. Despite more than 20 years research on IL-15, some controversial issues remain to be addressed. A first point concerns the detection of the sIL-15/IL-15Rα in plasma of healthy donors or patients with cancer and its biological significance. The second and third unsolved question regards the protumorigenic role of the IL-15/IL-15Rα complex in human cancer and the detrimental immunological consequences associated to prolonged exposure of natural killer (NK) cells to both forms of soluble IL-15, respectively. Data suggest that in vivo prolonged or repeated exposure to monomeric sIL-15 or the soluble complex may lead to NK hypo-responsiveness through the expansion of the CD8(+)/CD44(+) T cell subset that would suppress NK cell functions. In vitro experiments indicate that soluble complex and monomeric IL-15 may cause NK hyporesponsiveness through a direct effect caused by their prolonged stimulation, suggesting that this mechanism could also be effective in vivo. Therefore, a better knowledge of IL-15 and a more appropriate use of both its soluble forms, in terms of concentrations and time of exposure, are essential in order to improve their therapeutic use. In cancer, the overproduction of sIL-15/IL-15Rα could represent a novel mechanism of immune escape. The soluble complex may act as a decoy cytokine unable to efficiently foster NK cells, or could induce NK hyporesponsiveness through an excessive and prolonged stimulation depending on the type of IL-15Rα isoforms associated. All these unsolved questions are not merely limited to the knowledge of IL-15 pathophysiology, but are crucial also for the therapeutic use of this cytokine. Therefore, in this review, we will discuss key unanswered issues on the heterogeneity and biological significance of IL-15 isoforms, analyzing both their cancer-related biological functions and their therapeutic implications. BMJ Publishing Group 2020-11-17 /pmc/articles/PMC7674108/ /pubmed/33203664 http://dx.doi.org/10.1136/jitc-2020-001428 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Review
Fiore, Piera Filomena
Di Matteo, Sabina
Tumino, Nicola
Mariotti, Francesca Romana
Pietra, Gabriella
Ottonello, Selene
Negrini, Simone
Bottazzi, Barbara
Moretta, Lorenzo
Mortier, Erwan
Azzarone, Bruno
Interleukin-15 and cancer: some solved and many unsolved questions
title Interleukin-15 and cancer: some solved and many unsolved questions
title_full Interleukin-15 and cancer: some solved and many unsolved questions
title_fullStr Interleukin-15 and cancer: some solved and many unsolved questions
title_full_unstemmed Interleukin-15 and cancer: some solved and many unsolved questions
title_short Interleukin-15 and cancer: some solved and many unsolved questions
title_sort interleukin-15 and cancer: some solved and many unsolved questions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674108/
https://www.ncbi.nlm.nih.gov/pubmed/33203664
http://dx.doi.org/10.1136/jitc-2020-001428
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