NKTR-255, a novel polymer-conjugated rhIL-15 with potent antitumor efficacy.


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
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.

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Auteurs

Takahiro Miyazaki (T)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Mekhala Maiti (M)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Marlene Hennessy (M)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Thomas Chang (T)

Protein Chemistry, Nektar Therapeutics, San Francisco, California, USA.

Peiwen Kuo (P)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Murali Addepalli (M)

Research Biology, Nektar Therapeutics, Hyderabad, India.

Palakshi Obalapur (P)

Research Biology, Nektar Therapeutics, Hyderabad, India.

Sara Sheibani (S)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Joanna Wilczek (J)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Rhoneil Pena (R)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Phi Quach (P)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Janet Cetz (J)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Andrew Moffett (A)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Yinyan Tang (Y)

Protein Chemistry, Nektar Therapeutics, San Francisco, California, USA.

Peter Kirk (P)

Protein Chemistry, Nektar Therapeutics, San Francisco, California, USA.

Jicai Huang (J)

Protein Chemistry, Nektar Therapeutics, San Francisco, California, USA.

Dawei Sheng (D)

Protein Chemistry, Nektar Therapeutics, San Francisco, California, USA.

Ping Zhang (P)

Protein Chemistry, Nektar Therapeutics, San Francisco, California, USA.

Werner Rubas (W)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Loui Madakamutil (L)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Saul Kivimäe (S)

Research Biology: Pharmacology, Nektar Therapeutics, San Francisco, California, USA.

Jonathan Zalevsky (J)

Research and Development, Nektar Therapeutics, San Francisco, California, USA jzalevsky@nektar.com.

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Classifications MeSH