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Therapeutic Bispecific T-Cell Engager Antibody Targeting the Transferrin Receptor
Bispecific T-cell engager antibodies (BiTE) have been explored as a means to recruit cytolytic T cells to kill tumor cells. The transferrin receptor (TfR) is highly expressed on the surface of rapidly proliferating tumor cells. Therefore, it holds great potential in T cell redirecting therapies. In...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598450/ https://www.ncbi.nlm.nih.gov/pubmed/31293575 http://dx.doi.org/10.3389/fimmu.2019.01396 |
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author | Fu, Mingpeng He, Qi Guo, Zilong Zhou, Xiaoran Li, Heli Zhao, Liang Tang, Hongling Zhou, Xiaoqi Zhu, Huifen Shen, Guanxin He, Yong Lei, Ping |
author_facet | Fu, Mingpeng He, Qi Guo, Zilong Zhou, Xiaoran Li, Heli Zhao, Liang Tang, Hongling Zhou, Xiaoqi Zhu, Huifen Shen, Guanxin He, Yong Lei, Ping |
author_sort | Fu, Mingpeng |
collection | PubMed |
description | Bispecific T-cell engager antibodies (BiTE) have been explored as a means to recruit cytolytic T cells to kill tumor cells. The transferrin receptor (TfR) is highly expressed on the surface of rapidly proliferating tumor cells. Therefore, it holds great potential in T cell redirecting therapies. In this research, we developed a BiTE targeting TfR and CD3 (TfR-BiTE) and studied its therapeutic impact on TfR-positive cancer. TfR-BiTE had the ability to induce the selective lysis of various TfR-positive cancer cells through the activation of T cells, the release of cytokines, and then the coming proliferation of T cells, whereas TfR-negative cells were not affected. In a subcutaneous HepG2 xenograft model, low concentrations of TfR-BiTE inhibited tumor growth. Overall, these results reveal that TfR-BiTE can selectively deplete TfR-positive HepG2 cells; hence, it represents a novel immunotherapeutic approach for the treatment of hepatocellular carcinoma. |
format | Online Article Text |
id | pubmed-6598450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65984502019-07-10 Therapeutic Bispecific T-Cell Engager Antibody Targeting the Transferrin Receptor Fu, Mingpeng He, Qi Guo, Zilong Zhou, Xiaoran Li, Heli Zhao, Liang Tang, Hongling Zhou, Xiaoqi Zhu, Huifen Shen, Guanxin He, Yong Lei, Ping Front Immunol Immunology Bispecific T-cell engager antibodies (BiTE) have been explored as a means to recruit cytolytic T cells to kill tumor cells. The transferrin receptor (TfR) is highly expressed on the surface of rapidly proliferating tumor cells. Therefore, it holds great potential in T cell redirecting therapies. In this research, we developed a BiTE targeting TfR and CD3 (TfR-BiTE) and studied its therapeutic impact on TfR-positive cancer. TfR-BiTE had the ability to induce the selective lysis of various TfR-positive cancer cells through the activation of T cells, the release of cytokines, and then the coming proliferation of T cells, whereas TfR-negative cells were not affected. In a subcutaneous HepG2 xenograft model, low concentrations of TfR-BiTE inhibited tumor growth. Overall, these results reveal that TfR-BiTE can selectively deplete TfR-positive HepG2 cells; hence, it represents a novel immunotherapeutic approach for the treatment of hepatocellular carcinoma. Frontiers Media S.A. 2019-06-21 /pmc/articles/PMC6598450/ /pubmed/31293575 http://dx.doi.org/10.3389/fimmu.2019.01396 Text en Copyright © 2019 Fu, He, Guo, Zhou, Li, Zhao, Tang, Zhou, Zhu, Shen, He and Lei. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Fu, Mingpeng He, Qi Guo, Zilong Zhou, Xiaoran Li, Heli Zhao, Liang Tang, Hongling Zhou, Xiaoqi Zhu, Huifen Shen, Guanxin He, Yong Lei, Ping Therapeutic Bispecific T-Cell Engager Antibody Targeting the Transferrin Receptor |
title | Therapeutic Bispecific T-Cell Engager Antibody Targeting the Transferrin Receptor |
title_full | Therapeutic Bispecific T-Cell Engager Antibody Targeting the Transferrin Receptor |
title_fullStr | Therapeutic Bispecific T-Cell Engager Antibody Targeting the Transferrin Receptor |
title_full_unstemmed | Therapeutic Bispecific T-Cell Engager Antibody Targeting the Transferrin Receptor |
title_short | Therapeutic Bispecific T-Cell Engager Antibody Targeting the Transferrin Receptor |
title_sort | therapeutic bispecific t-cell engager antibody targeting the transferrin receptor |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598450/ https://www.ncbi.nlm.nih.gov/pubmed/31293575 http://dx.doi.org/10.3389/fimmu.2019.01396 |
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