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Bispecific T cell engagers: an emerging therapy for management of hematologic malignancies
Harnessing the power of immune cells, especially T cells, to enhance anti-tumor activities has become a promising strategy in clinical management of hematologic malignancies. The emerging bispecific antibodies (BsAbs), which recruit T cells to tumor cells, exemplified by bispecific T cell engagers (...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091790/ https://www.ncbi.nlm.nih.gov/pubmed/33941237 http://dx.doi.org/10.1186/s13045-021-01084-4 |
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author | Tian, Zheng Liu, Ming Zhang, Ya Wang, Xin |
author_facet | Tian, Zheng Liu, Ming Zhang, Ya Wang, Xin |
author_sort | Tian, Zheng |
collection | PubMed |
description | Harnessing the power of immune cells, especially T cells, to enhance anti-tumor activities has become a promising strategy in clinical management of hematologic malignancies. The emerging bispecific antibodies (BsAbs), which recruit T cells to tumor cells, exemplified by bispecific T cell engagers (BiTEs), have facilitated the development of tumor immunotherapy. Here we discussed the advances and challenges in BiTE therapy developed for the treatment of hematologic malignancies. Blinatumomab, the first BiTE approved for the treatment of acute lymphocytic leukemia (ALL), is appreciated for its high efficacy and safety. Recent studies have focused on improving the efficacy of BiTEs by optimizing treatment regimens and refining the molecular structures of BiTEs. A considerable number of bispecific T cell-recruiting antibodies which are potentially effective in hematologic malignancies have been derived from BiTEs. The elucidation of mechanisms of BiTE action and neonatal techniques used for the construction of BsAbs can improve the treatment of hematological malignancies. This review summarized the features of bispecific T cell-recruiting antibodies for the treatment of hematologic malignancies with special focus on preclinical experiments and clinical studies. |
format | Online Article Text |
id | pubmed-8091790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80917902021-05-04 Bispecific T cell engagers: an emerging therapy for management of hematologic malignancies Tian, Zheng Liu, Ming Zhang, Ya Wang, Xin J Hematol Oncol Review Harnessing the power of immune cells, especially T cells, to enhance anti-tumor activities has become a promising strategy in clinical management of hematologic malignancies. The emerging bispecific antibodies (BsAbs), which recruit T cells to tumor cells, exemplified by bispecific T cell engagers (BiTEs), have facilitated the development of tumor immunotherapy. Here we discussed the advances and challenges in BiTE therapy developed for the treatment of hematologic malignancies. Blinatumomab, the first BiTE approved for the treatment of acute lymphocytic leukemia (ALL), is appreciated for its high efficacy and safety. Recent studies have focused on improving the efficacy of BiTEs by optimizing treatment regimens and refining the molecular structures of BiTEs. A considerable number of bispecific T cell-recruiting antibodies which are potentially effective in hematologic malignancies have been derived from BiTEs. The elucidation of mechanisms of BiTE action and neonatal techniques used for the construction of BsAbs can improve the treatment of hematological malignancies. This review summarized the features of bispecific T cell-recruiting antibodies for the treatment of hematologic malignancies with special focus on preclinical experiments and clinical studies. BioMed Central 2021-05-03 /pmc/articles/PMC8091790/ /pubmed/33941237 http://dx.doi.org/10.1186/s13045-021-01084-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Tian, Zheng Liu, Ming Zhang, Ya Wang, Xin Bispecific T cell engagers: an emerging therapy for management of hematologic malignancies |
title | Bispecific T cell engagers: an emerging therapy for management of hematologic malignancies |
title_full | Bispecific T cell engagers: an emerging therapy for management of hematologic malignancies |
title_fullStr | Bispecific T cell engagers: an emerging therapy for management of hematologic malignancies |
title_full_unstemmed | Bispecific T cell engagers: an emerging therapy for management of hematologic malignancies |
title_short | Bispecific T cell engagers: an emerging therapy for management of hematologic malignancies |
title_sort | bispecific t cell engagers: an emerging therapy for management of hematologic malignancies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091790/ https://www.ncbi.nlm.nih.gov/pubmed/33941237 http://dx.doi.org/10.1186/s13045-021-01084-4 |
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