Carcinoembryonic Antigen (CEA)-Specific 4-1BB-Costimulation Induced by CEA-Targeted 4-1BB-Agonistic Trimerbodies.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2019
Historique:
received: 30 03 2019
accepted: 16 07 2019
entrez: 17 8 2019
pubmed: 17 8 2019
medline: 30 9 2020
Statut: epublish

Résumé

4-1BB (CD137) is an inducible costimulatory receptor that promotes expansion and survival of activated T cells; and IgG-based 4-1BB-agonistic monoclonal antibodies exhibited potent antitumor activity in clinical trials. However, the clinical development of those antibodies is restricted by major off-tumor toxicities associated with FcγR interactions. We have recently generated an EGFR-targeted 4-1BB-agonistic trimerbody that demonstrated strong antitumor activity and did not induce systemic inflammatory cytokine secretion and hepatotoxicity associated with first-generation 4-1BB agonists. Here, we generate a bispecific 4-1BB-agonistic trimerbody targeting the carcinoembryonic antigen (CEA) that is highly expressed in cancers of diverse origins. The CEA-targeted anti-4-1BB-agonistic trimerbody consists of three 4-1BB-specific single-chain fragment variable antibodies and three anti-CEA single-domain antibodies positioned around a murine collagen XVIII-derived homotrimerization domain. The trimerbody was produced as a homogenous, non-aggregating, soluble protein purifiable by standard affinity chromatographic methods. The purified trimerbody was found to be trimeric in solution, very efficient at recognizing 4-1BB and CEA, and potently costimulating T cells

Identifiants

pubmed: 31417564
doi: 10.3389/fimmu.2019.01791
pmc: PMC6685135
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Carcinoembryonic Antigen 0
Recombinant Proteins 0
Single-Chain Antibodies 0
Tumor Necrosis Factor Receptor Superfamily, Member 9 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1791

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Auteurs

Kasper Mikkelsen (K)

Immunotherapy and Cell Engineering Laboratory, Department of Engineering, Aarhus University, Aarhus, Denmark.

Seandean Lykke Harwood (SL)

Immunotherapy and Cell Engineering Laboratory, Department of Engineering, Aarhus University, Aarhus, Denmark.

Marta Compte (M)

Department of Antibody Engineering, Leadartis SL, Madrid, Spain.

Nekane Merino (N)

Structural Biology Unit, CIC bioGUNE, Parque Tecnológico de Bizkaia, Derio, Spain.

Kasper Mølgaard (K)

Immunotherapy and Cell Engineering Laboratory, Department of Engineering, Aarhus University, Aarhus, Denmark.

Simon Lykkemark (S)

Immunotherapy and Cell Engineering Laboratory, Department of Engineering, Aarhus University, Aarhus, Denmark.

Ana Alvarez-Mendez (A)

Department of Nursing, Universidad Complutense de Madrid, Madrid, Spain.

Francisco J Blanco (FJ)

Structural Biology Unit, CIC bioGUNE, Parque Tecnológico de Bizkaia, Derio, Spain.
IKERBASQUE, Basque Foundation for Science, Bilbao, Spain.

Luis Álvarez-Vallina (L)

Immunotherapy and Cell Engineering Laboratory, Department of Engineering, Aarhus University, Aarhus, Denmark.
Cancer Immunotherapy Unit (UNICA), Department of Immunology, Hospital Universitario 12 de Octubre, Madrid, Spain.
Immuno-Oncology and Immunotherapy Group, Instituto de Investigación Sanitaria 12 de Octubre (i+12), Madrid, Spain.

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Classifications MeSH