Tumor-Homing Antibody-Cytokine Fusions for Cancer Therapy.

activity on demand antibody-cytokine fusion proteins cancer therapy dual-cytokine products

Journal

OncoTargets and therapy
ISSN: 1178-6930
Titre abrégé: Onco Targets Ther
Pays: New Zealand
ID NLM: 101514322

Informations de publication

Date de publication:
2024
Historique:
received: 12 07 2024
accepted: 19 08 2024
medline: 3 9 2024
pubmed: 3 9 2024
entrez: 3 9 2024
Statut: epublish

Résumé

Recombinant cytokine products have emerged as a promising avenue in cancer therapy due to their capacity to modulate and enhance the immune response against tumors. However, their clinical application is significantly hindered by systemic toxicities already at low doses, thus preventing escalation to therapeutically active regimens. One promising approach to overcoming these limitations is using antibody-cytokine fusion proteins (also called immunocytokines). These biopharmaceuticals leverage the targeting specificity of antibodies to deliver cytokines directly to the tumor microenvironment, thereby reducing systemic exposure and enhancing the therapeutic index. This review comprehensively examines the development and potential of antibody-cytokine fusion proteins in cancer therapy. It explores the molecular characteristics that influence the performance of these fusion proteins, and it highlights key findings from preclinical and clinical studies, illustrating the potential of immunocytokines to improve treatment outcomes in cancer patients. Recent advancements in the field, such as novel engineering strategies and combination strategies to enhance the efficacy and safety of immunocytokines, are also discussed. These innovations offer new opportunities to optimize this class of biotherapeutics, making them a more viable and effective option for cancer treatment. As the field continues to evolve, understanding the critical factors that influence the performance of immunocytokines will be essential for successfully translating these therapies into clinical practice.

Identifiants

pubmed: 39224695
doi: 10.2147/OTT.S480787
pii: 480787
pmc: PMC11368152
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

697-715

Informations de copyright

© 2024 Prodi et al.

Déclaration de conflit d'intérêts

Dario Neri is a co-founder and shareholder of Philogen (www.philogen.com), a Swiss-Italian Biotech company that operates in the field of ligand-based pharmacodelivery. Eleonora Prodi and Roberto De Luca are employees of Philochem AG, a daughter company of Philogen acting as discovery unit of the group. The authors report no other conflicts of interest in this work.

Auteurs

Eleonora Prodi (E)

Philochem AG, Otelfingen, 8112, Switzerland.
University of Trento, Italy, CiBIO (Department of Cellular, Computational and Integrative Biology), Povo, 38123, Trento.

Dario Neri (D)

Philogen Spa, Siena, 53100, Italy.
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH Zürich), Zurich, Switzerland.

Roberto De Luca (R)

Philochem AG, Otelfingen, 8112, Switzerland.

Classifications MeSH