Cargando…

T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell

Triplebody 19-3-19, an antibody-derived protein, carries three single chain fragment variable domains in tandem in a single polypeptide chain. 19-3-19 binds CD19-bearing lymphoid cells via its two distal domains and primary T cells via its CD3-targeting central domain in an antigen-specific manner....

Descripción completa

Detalles Bibliográficos
Autores principales: Roskopf, Claudia C., Schiller, Christian B., Braciak, Todd A., Kobold, Sebastian, Schubert, Ingo A., Fey, Georg H., Hopfner, Karl-Peter, Oduncu, Fuat S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171644/
https://www.ncbi.nlm.nih.gov/pubmed/25115385
_version_ 1782335930581909504
author Roskopf, Claudia C.
Schiller, Christian B.
Braciak, Todd A.
Kobold, Sebastian
Schubert, Ingo A.
Fey, Georg H.
Hopfner, Karl-Peter
Oduncu, Fuat S.
author_facet Roskopf, Claudia C.
Schiller, Christian B.
Braciak, Todd A.
Kobold, Sebastian
Schubert, Ingo A.
Fey, Georg H.
Hopfner, Karl-Peter
Oduncu, Fuat S.
author_sort Roskopf, Claudia C.
collection PubMed
description Triplebody 19-3-19, an antibody-derived protein, carries three single chain fragment variable domains in tandem in a single polypeptide chain. 19-3-19 binds CD19-bearing lymphoid cells via its two distal domains and primary T cells via its CD3-targeting central domain in an antigen-specific manner. Here, malignant B-lymphoid cell lines and primary cells from patients with B cell malignancies were used as targets in cytotoxicity tests with pre-stimulated allogeneic T cells as effectors. 19-3-19 mediated up to 95% specific lysis of CD19-positive tumor cells and, at picomolar EC(50) doses, had similar cytolytic potency as the clinically successful agent Blinatumomab(TM). 19-3-19 activated resting T cells from healthy unrelated donors and mediated specific lysis of both autologous and allogeneic CD19-positive cells. 19-3-19 led to the elimination of 70% of CD19-positive target cells even with resting T cells as effectors at an effector-to-target cell ratio of 1 : 10. The molecule is therefore capable of mediating serial lysis of target cells by a single T cell. These results highlight that central domains capable of engaging different immune effectors can be incorporated into the triplebody format to provide more individualized therapy tailored to a patient’s specific immune status.
format Online
Article
Text
id pubmed-4171644
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-41716442014-09-23 T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell Roskopf, Claudia C. Schiller, Christian B. Braciak, Todd A. Kobold, Sebastian Schubert, Ingo A. Fey, Georg H. Hopfner, Karl-Peter Oduncu, Fuat S. Oncotarget Research Paper Triplebody 19-3-19, an antibody-derived protein, carries three single chain fragment variable domains in tandem in a single polypeptide chain. 19-3-19 binds CD19-bearing lymphoid cells via its two distal domains and primary T cells via its CD3-targeting central domain in an antigen-specific manner. Here, malignant B-lymphoid cell lines and primary cells from patients with B cell malignancies were used as targets in cytotoxicity tests with pre-stimulated allogeneic T cells as effectors. 19-3-19 mediated up to 95% specific lysis of CD19-positive tumor cells and, at picomolar EC(50) doses, had similar cytolytic potency as the clinically successful agent Blinatumomab(TM). 19-3-19 activated resting T cells from healthy unrelated donors and mediated specific lysis of both autologous and allogeneic CD19-positive cells. 19-3-19 led to the elimination of 70% of CD19-positive target cells even with resting T cells as effectors at an effector-to-target cell ratio of 1 : 10. The molecule is therefore capable of mediating serial lysis of target cells by a single T cell. These results highlight that central domains capable of engaging different immune effectors can be incorporated into the triplebody format to provide more individualized therapy tailored to a patient’s specific immune status. Impact Journals LLC 2014-07-23 /pmc/articles/PMC4171644/ /pubmed/25115385 Text en Copyright: © 2014 Roskopf et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Roskopf, Claudia C.
Schiller, Christian B.
Braciak, Todd A.
Kobold, Sebastian
Schubert, Ingo A.
Fey, Georg H.
Hopfner, Karl-Peter
Oduncu, Fuat S.
T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell
title T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell
title_full T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell
title_fullStr T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell
title_full_unstemmed T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell
title_short T cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant B-lymphoid cells by a single T cell
title_sort t cell-recruiting triplebody 19-3-19 mediates serial lysis of malignant b-lymphoid cells by a single t cell
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171644/
https://www.ncbi.nlm.nih.gov/pubmed/25115385
work_keys_str_mv AT roskopfclaudiac tcellrecruitingtriplebody19319mediatesseriallysisofmalignantblymphoidcellsbyasingletcell
AT schillerchristianb tcellrecruitingtriplebody19319mediatesseriallysisofmalignantblymphoidcellsbyasingletcell
AT braciaktodda tcellrecruitingtriplebody19319mediatesseriallysisofmalignantblymphoidcellsbyasingletcell
AT koboldsebastian tcellrecruitingtriplebody19319mediatesseriallysisofmalignantblymphoidcellsbyasingletcell
AT schubertingoa tcellrecruitingtriplebody19319mediatesseriallysisofmalignantblymphoidcellsbyasingletcell
AT feygeorgh tcellrecruitingtriplebody19319mediatesseriallysisofmalignantblymphoidcellsbyasingletcell
AT hopfnerkarlpeter tcellrecruitingtriplebody19319mediatesseriallysisofmalignantblymphoidcellsbyasingletcell
AT oduncufuats tcellrecruitingtriplebody19319mediatesseriallysisofmalignantblymphoidcellsbyasingletcell