NKTR-255, a novel polymer-conjugated rhIL-15 with potent antitumor efficacy.
Animals
Antineoplastic Agents
/ pharmacokinetics
Burkitt Lymphoma
/ drug therapy
Cell Degranulation
/ drug effects
Cell Line, Tumor
Cell Proliferation
/ drug effects
Cytokines
/ metabolism
Female
HEK293 Cells
Humans
Interleukin-15
/ pharmacokinetics
Lymphocyte Activation
/ drug effects
Lymphocytes
/ drug effects
Mice, Inbred BALB C
Mice, Inbred C57BL
Mice, Knockout
Mice, SCID
Polyethylene Glycols
/ pharmacokinetics
Receptors, Interleukin-15
/ agonists
Signal Transduction
Tumor Microenvironment
hematologic neoplasms
immunotherapy
natural killer T-cells
Journal
Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
accepted:
20
04
2021
entrez:
18
5
2021
pubmed:
19
5
2021
medline:
6
1
2022
Statut:
ppublish
Résumé
NKTR-255 is a novel polyethylene glycol-conjugate of recombinant human interleukin-15 (rhIL-15), which was designed to retain all known receptor binding interactions of the IL-15 molecule. We explored the biologic and pharmacologic differences between endogenous IL-15 receptor α (IL-15Rα)-dependent (NKTR-255 and rhIL-15) and IL-15Rα-independent (precomplexed rhIL-15/IL-15Rα) cytokines. In vitro pharmacological properties of rhIL-15, NKTR-255 and precomplex cytokines (rhIL-15/IL-15Rα and rhIL-15 N72D/IL-15Rα Fc) were investigated in receptor binding, signaling and cell function. In vivo pharmacokinetic (PK) and pharmacodynamic profile of the cytokines were evaluated in normal mice. Finally, immunomodulatory effect and antitumor activity were assessed in a Daudi lymphoma model. NKTR-255 and rhIL-15 exhibited similar in vitro properties in receptor affinity, signaling and leukocyte degranulation, which collectively differed from precomplexed cytokines. Notably, NKTR-255 and rhIL-15 stimulated greater granzyme B secretion in human peripheral blood mononuclear cells versus precomplexed cytokines. In vivo, NKTR-255 exhibited a PK profile with reduced clearance and a longer half-life relative to rhIL-15 and demonstrated prolonged IL-15R engagement in lymphocytes compared with only transient engagement observed for rhIL-15 and precomplexed rhIL-15 N72D/IL-15Rα Fc. As a consequent, NKTR-255 provided a durable and sustained proliferation and activation of natural killer (NK) and CD8 Our results show that the novel immunotherapeutic, NKTR-255, retains the full spectrum of IL-15 biology, but with improved PK properties, over rhIL-15. These findings support the ongoing phase 1 first-in-human trial (NCT04136756) of NKTR-255 in participants with relapsed or refractory hematologic malignancies, potentially advancing rhIL-15-based immunotherapies for the treatment of cancer.
Sections du résumé
BACKGROUND
NKTR-255 is a novel polyethylene glycol-conjugate of recombinant human interleukin-15 (rhIL-15), which was designed to retain all known receptor binding interactions of the IL-15 molecule. We explored the biologic and pharmacologic differences between endogenous IL-15 receptor α (IL-15Rα)-dependent (NKTR-255 and rhIL-15) and IL-15Rα-independent (precomplexed rhIL-15/IL-15Rα) cytokines.
METHODS
In vitro pharmacological properties of rhIL-15, NKTR-255 and precomplex cytokines (rhIL-15/IL-15Rα and rhIL-15 N72D/IL-15Rα Fc) were investigated in receptor binding, signaling and cell function. In vivo pharmacokinetic (PK) and pharmacodynamic profile of the cytokines were evaluated in normal mice. Finally, immunomodulatory effect and antitumor activity were assessed in a Daudi lymphoma model.
RESULTS
NKTR-255 and rhIL-15 exhibited similar in vitro properties in receptor affinity, signaling and leukocyte degranulation, which collectively differed from precomplexed cytokines. Notably, NKTR-255 and rhIL-15 stimulated greater granzyme B secretion in human peripheral blood mononuclear cells versus precomplexed cytokines. In vivo, NKTR-255 exhibited a PK profile with reduced clearance and a longer half-life relative to rhIL-15 and demonstrated prolonged IL-15R engagement in lymphocytes compared with only transient engagement observed for rhIL-15 and precomplexed rhIL-15 N72D/IL-15Rα Fc. As a consequent, NKTR-255 provided a durable and sustained proliferation and activation of natural killer (NK) and CD8
CONCLUSIONS
Our results show that the novel immunotherapeutic, NKTR-255, retains the full spectrum of IL-15 biology, but with improved PK properties, over rhIL-15. These findings support the ongoing phase 1 first-in-human trial (NCT04136756) of NKTR-255 in participants with relapsed or refractory hematologic malignancies, potentially advancing rhIL-15-based immunotherapies for the treatment of cancer.
Identifiants
pubmed: 34001523
pii: jitc-2020-002024
doi: 10.1136/jitc-2020-002024
pmc: PMC8130760
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Cytokines
0
IL15 protein, human
0
IL15RA protein, human
0
Il15ra protein, mouse
0
Interleukin-15
0
NKTR-255
0
Receptors, Interleukin-15
0
Polyethylene Glycols
3WJQ0SDW1A
Banques de données
ClinicalTrials.gov
['NCT04136756']
Types de publication
Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: All authors are current or former employees of Nektar Therapeutics and/or have Nektar Therapeutics stock ownership interests to disclose. PKu is currently employed by Gilead Sciences. MA is currently employed by HIBC Biopharma. PKi is currently employed by Immunocore. LM is currently employed by Invivoscribe.
Références
Immunity. 2002 Nov;17(5):537-47
pubmed: 12433361
J Clin Oncol. 2015 Jan 1;33(1):74-82
pubmed: 25403209
Proc Natl Acad Sci U S A. 2020 Jan 7;117(1):522-531
pubmed: 31871169
J Mol Biol. 2008 Sep 26;382(1):1-12
pubmed: 18656487
Immunity. 1998 Nov;9(5):669-76
pubmed: 9846488
Blood. 2001 Jan 1;97(1):14-32
pubmed: 11133738
Clin Cancer Res. 2019 Aug 15;25(16):4945-4954
pubmed: 31142503
Immunol Lett. 2017 Oct;190:159-168
pubmed: 28823521
J Exp Med. 2000 Mar 6;191(5):771-80
pubmed: 10704459
Blood. 2012 Jul 5;120(1):e1-8
pubmed: 22496150
J Cell Sci. 2019 Dec 5;133(5):
pubmed: 31653781
Lancet Oncol. 2018 May;19(5):694-704
pubmed: 29628312
Cell Mol Immunol. 2008 Jun;5(3):189-96
pubmed: 18582400
EMBO J. 1994 Jun 15;13(12):2822-30
pubmed: 8026467
Cancer Immunol Res. 2016 Jan;4(1):49-60
pubmed: 26511282
Clin Cancer Res. 2014 Apr 15;20(8):2044-50
pubmed: 24737791
EMBO J. 1995 Aug 1;14(15):3654-63
pubmed: 7641685
J Cell Biol. 1995 Apr;129(1):55-64
pubmed: 7698995
Curr Urol Rep. 2019 Nov 28;20(12):84
pubmed: 31781942
J Biol Chem. 2006 Jan 20;281(3):1612-9
pubmed: 16284400
Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):1969-74
pubmed: 14762166
Blood. 2009 Sep 17;114(12):2417-26
pubmed: 19605850
Eur Cytokine Netw. 2010 Dec;21(4):297-307
pubmed: 21078585
Nat Rev Immunol. 2003 Apr;3(4):269-79
pubmed: 12669018
Expert Opin Biol Ther. 2020 Jul;20(7):705-709
pubmed: 32159390
Proc Natl Acad Sci U S A. 2010 Dec 14;107(50):21647-52
pubmed: 21098276