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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....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171644/ https://www.ncbi.nlm.nih.gov/pubmed/25115385 |
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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 |
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