An IL-7 fusion protein targeting EDA fibronectin upregulates TCF1 on CD8+ T-cells, preferentially accumulates to neoplastic lesions, and boosts PD-1 blockade.


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:
13 Aug 2024
Historique:
accepted: 27 07 2024
medline: 15 8 2024
pubmed: 15 8 2024
entrez: 14 8 2024
Statut: epublish

Résumé

Anti-PD-1 antibodies have revolutionized cancer immunotherapy due to their ability to induce long-lasting complete remissions in a proportion of patients. Current research efforts are attempting to identify biomarkers and suitable combination partners to predict or further improve the activity of immune checkpoint inhibitors. Antibody-cytokine fusions are a class of pharmaceuticals that showed the potential to boost the anticancer properties of other immunotherapies. Extradomain A-fibronectin (EDA-FN), which is expressed in most solid and hematological tumors but is virtually undetectable in healthy adult tissues, is an attractive target for the delivery of cytokine at the site of the disease. In this work, we describe the generation and characterization of a novel interleukin-7-based fusion protein targeting EDA-FN termed F8(scDb)-IL7. The product consists of the F8 antibody specific to the alternatively spliced EDA of FN in the single-chain diabody (scDb) format fused to human IL-7. F8(scDb)-IL7 efficiently stimulates human peripheral blood mononuclear cells in vitro. Moreover, the product significantly increases the expression of T Cell Factor 1 (TCF-1) on CD8+T cells compared with an IL2-fusion protein. TCF-1 has emerged as a pivotal transcription factor that influences the durability and potency of immune responses against tumors. In preclinical cancer models, F8(scDb)-IL7 demonstrates potent single-agent activity and eradicates sarcoma lesions when combined with anti-PD-1. Our results provide the rationale to explore the combination of F8(scDb)-IL7 with anti-PD-1 antibodies for the treatment of patients with cancer.

Sections du résumé

BACKGROUND BACKGROUND
Anti-PD-1 antibodies have revolutionized cancer immunotherapy due to their ability to induce long-lasting complete remissions in a proportion of patients. Current research efforts are attempting to identify biomarkers and suitable combination partners to predict or further improve the activity of immune checkpoint inhibitors. Antibody-cytokine fusions are a class of pharmaceuticals that showed the potential to boost the anticancer properties of other immunotherapies. Extradomain A-fibronectin (EDA-FN), which is expressed in most solid and hematological tumors but is virtually undetectable in healthy adult tissues, is an attractive target for the delivery of cytokine at the site of the disease.
METHODS METHODS
In this work, we describe the generation and characterization of a novel interleukin-7-based fusion protein targeting EDA-FN termed F8(scDb)-IL7. The product consists of the F8 antibody specific to the alternatively spliced EDA of FN in the single-chain diabody (scDb) format fused to human IL-7.
RESULTS RESULTS
F8(scDb)-IL7 efficiently stimulates human peripheral blood mononuclear cells in vitro. Moreover, the product significantly increases the expression of T Cell Factor 1 (TCF-1) on CD8+T cells compared with an IL2-fusion protein. TCF-1 has emerged as a pivotal transcription factor that influences the durability and potency of immune responses against tumors. In preclinical cancer models, F8(scDb)-IL7 demonstrates potent single-agent activity and eradicates sarcoma lesions when combined with anti-PD-1.
CONCLUSIONS CONCLUSIONS
Our results provide the rationale to explore the combination of F8(scDb)-IL7 with anti-PD-1 antibodies for the treatment of patients with cancer.

Identifiants

pubmed: 39142716
pii: jitc-2023-008504
doi: 10.1136/jitc-2023-008504
pii:
doi:

Substances chimiques

Fibronectins 0
Interleukin-7 0
Recombinant Fusion Proteins 0
Programmed Cell Death 1 Receptor 0
Hepatocyte Nuclear Factor 1-alpha 0
PDCD1 protein, human 0
Immune Checkpoint Inhibitors 0
IL7 protein, human 0
HNF1A protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. 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: DN is a cofounder and shareholder of Philogen (www.philogen.com), a Swiss-Italian Biotech company that operates in the field of ligand-based pharmacodelivery. CDN, EProdi, RD, DR, EG and EPuca are employees of Philochem AG, a daughter company of Philogen acting as discovery unit of the group.

Auteurs

Cesare Di Nitto (C)

Philochem AG, Otelfingen, Switzerland.

Domenico Ravazza (D)

Philochem AG, Otelfingen, Switzerland.

Ettore Gilardoni (E)

Philochem AG, Otelfingen, Switzerland.

Thomas Look (T)

Department of Neurology and Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.

Miaomiao Sun (M)

Department of Neurology and Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.

Eleonora Prodi (E)

Philochem AG, Otelfingen, Switzerland.

Vlad Moisoiu (V)

Department of Neurology and Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.

Christian Pellegrino (C)

Department of Medical Oncology and Hematology, University Hospital Zurich, Zurich, Switzerland.

Markus G Manz (MG)

Department of Medical Oncology and Hematology, University Hospital Zurich, Zurich, Switzerland.

Emanuele Puca (E)

Philochem AG, Otelfingen, Switzerland.

Michael Weller (M)

Department of Neurology and Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.
University of Zurich, Zurich, Switzerland.

Tobias Weiss (T)

Department of Neurology and Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland.
University of Zurich, Zurich, Switzerland.

Dario Neri (D)

Philogen SpA, Siena, Italy.
Department of Chemistry and Applied Biosciences, ETH Zurich, Zurich, Switzerland.

Roberto De Luca (R)

Philochem AG, Otelfingen, Switzerland roberto.deluca@philogen.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH