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Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells

With their resistance to genotoxic and anti-proliferative drugs and potential to grow tumors and metastases from very few cells, cancer stem or tumor-initiating cells (TICs) are a severe limitation for the treatment of cancer by conventional therapies. Here, we explored whether human T cells that ar...

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Autores principales: Herrmann, Ines, Baeuerle, Patrick A., Friedrich, Matthias, Murr, Alexander, Filusch, Susanne, Rüttinger, Dominik, Majdoub, Mariam W., Sharma, Sherven, Kufer, Peter, Raum, Tobias, Münz, Markus
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956687/
https://www.ncbi.nlm.nih.gov/pubmed/20976159
http://dx.doi.org/10.1371/journal.pone.0013474
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author Herrmann, Ines
Baeuerle, Patrick A.
Friedrich, Matthias
Murr, Alexander
Filusch, Susanne
Rüttinger, Dominik
Majdoub, Mariam W.
Sharma, Sherven
Kufer, Peter
Raum, Tobias
Münz, Markus
author_facet Herrmann, Ines
Baeuerle, Patrick A.
Friedrich, Matthias
Murr, Alexander
Filusch, Susanne
Rüttinger, Dominik
Majdoub, Mariam W.
Sharma, Sherven
Kufer, Peter
Raum, Tobias
Münz, Markus
author_sort Herrmann, Ines
collection PubMed
description With their resistance to genotoxic and anti-proliferative drugs and potential to grow tumors and metastases from very few cells, cancer stem or tumor-initiating cells (TICs) are a severe limitation for the treatment of cancer by conventional therapies. Here, we explored whether human T cells that are redirected via an EpCAM/CD3-bispecific antibody called MT110 can lyse colorectal TICs and prevent tumor growth from TICs. MT110 recognizes EpCAM, a cell adhesion molecule expressed on TICs from diverse human carcinoma, which was recently shown to promote tumor growth through engagement of elements of the wnt pathway. MT110 was highly potent in mediating complete redirected lysis of KRAS-, PI3 kinase- and BRAF-mutated colorectal TICs, as demonstrated in a soft agar assay. In immunodeficient mice, MT110 prevented growth of tumors from a 5,000-fold excess of a minimally tumorigenic TIC dose. T cells engaged by MT110 may provide a potent therapeutic means to eradicate TICs and bulk tumor cells derived thereof.
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spelling pubmed-29566872010-10-25 Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells Herrmann, Ines Baeuerle, Patrick A. Friedrich, Matthias Murr, Alexander Filusch, Susanne Rüttinger, Dominik Majdoub, Mariam W. Sharma, Sherven Kufer, Peter Raum, Tobias Münz, Markus PLoS One Research Article With their resistance to genotoxic and anti-proliferative drugs and potential to grow tumors and metastases from very few cells, cancer stem or tumor-initiating cells (TICs) are a severe limitation for the treatment of cancer by conventional therapies. Here, we explored whether human T cells that are redirected via an EpCAM/CD3-bispecific antibody called MT110 can lyse colorectal TICs and prevent tumor growth from TICs. MT110 recognizes EpCAM, a cell adhesion molecule expressed on TICs from diverse human carcinoma, which was recently shown to promote tumor growth through engagement of elements of the wnt pathway. MT110 was highly potent in mediating complete redirected lysis of KRAS-, PI3 kinase- and BRAF-mutated colorectal TICs, as demonstrated in a soft agar assay. In immunodeficient mice, MT110 prevented growth of tumors from a 5,000-fold excess of a minimally tumorigenic TIC dose. T cells engaged by MT110 may provide a potent therapeutic means to eradicate TICs and bulk tumor cells derived thereof. Public Library of Science 2010-10-18 /pmc/articles/PMC2956687/ /pubmed/20976159 http://dx.doi.org/10.1371/journal.pone.0013474 Text en Herrmann et al. http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Herrmann, Ines
Baeuerle, Patrick A.
Friedrich, Matthias
Murr, Alexander
Filusch, Susanne
Rüttinger, Dominik
Majdoub, Mariam W.
Sharma, Sherven
Kufer, Peter
Raum, Tobias
Münz, Markus
Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells
title Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells
title_full Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells
title_fullStr Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells
title_full_unstemmed Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells
title_short Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells
title_sort highly efficient elimination of colorectal tumor-initiating cells by an epcam/cd3-bispecific antibody engaging human t cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956687/
https://www.ncbi.nlm.nih.gov/pubmed/20976159
http://dx.doi.org/10.1371/journal.pone.0013474
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