T cell receptor-directed antibody-drug conjugates for the treatment of T cell-derived cancers.

T cell leukemia T cell lymphoma T cell receptor antibody-drug conjugate idiotype targeted therapy yeast surface display

Journal

Molecular therapy. Oncology
ISSN: 2950-3299
Titre abrégé: Mol Ther Oncol
Pays: United States
ID NLM: 9918752083706676

Informations de publication

Date de publication:
19 Sep 2024
Historique:
received: 30 03 2024
revised: 02 07 2024
accepted: 16 07 2024
medline: 23 8 2024
pubmed: 23 8 2024
entrez: 23 8 2024
Statut: epublish

Résumé

T cell-derived cancers are hallmarked by heterogeneity, aggressiveness, and poor clinical outcomes. Available targeted therapies are severely limited due to a lack of target antigens that allow discrimination of malignant from healthy T cells. Here, we report a novel approach for the treatment of T cell diseases based on targeting the clonally rearranged T cell receptor displayed by the cancerous T cell population. As a proof of concept, we identified an antibody with unique specificity toward a distinct T cell receptor (TCR) and developed antibody-drug conjugates, precisely recognizing and eliminating target T cells while preserving overall T cell repertoire integrity and cellular immunity. Our anti-TCR antibody-drug conjugates demonstrated effective receptor-mediated cell internalization, associated with induction of cancer cell death with strong signs of apoptosis. Furthermore, cell proliferation-inhibiting bystander effects observed on target-negative cells may contribute to the molecules' anti-tumor properties precluding potential tumor escape mechanisms. To our knowledge, this represents the first anti-TCR antibody-drug conjugate designed as custom-tailored immunotherapy for T cell-driven pathologies.

Identifiants

pubmed: 39176070
doi: 10.1016/j.omton.2024.200850
pii: S2950-3299(24)00092-4
pmc: PMC11338945
doi:

Types de publication

Journal Article

Langues

eng

Pagination

200850

Informations de copyright

© 2024 The Author(s).

Déclaration de conflit d'intérêts

The authors declare no competing interests.

Auteurs

Katrin Schoenfeld (K)

Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, 64287 Darmstadt, Germany.

Jan Habermann (J)

Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Goethe University, Department of Pediatrics, Experimental Immunology and Cell Therapy, 60590 Frankfurt am Main, Germany.
Frankfurt Cancer Institute, Goethe University, 60596 Frankfurt am Main, Germany.

Philipp Wendel (P)

Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Goethe University, Department of Pediatrics, Experimental Immunology and Cell Therapy, 60590 Frankfurt am Main, Germany.
Frankfurt Cancer Institute, Goethe University, 60596 Frankfurt am Main, Germany.
German Cancer Consortium (DKTK), partner site Frankfurt/Mainz, 60590 Frankfurt am Main, Germany.
German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.

Julia Harwardt (J)

Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, 64287 Darmstadt, Germany.

Evelyn Ullrich (E)

Goethe University, Department of Pediatrics, Experimental Immunology and Cell Therapy, 60590 Frankfurt am Main, Germany.
Frankfurt Cancer Institute, Goethe University, 60596 Frankfurt am Main, Germany.
German Cancer Consortium (DKTK), partner site Frankfurt/Mainz, 60590 Frankfurt am Main, Germany.

Harald Kolmar (H)

Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Centre for Synthetic Biology, Technical University of Darmstadt, 64283 Darmstadt, Germany.

Classifications MeSH