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Recent advances of bispecific antibodies in solid tumors
Cancer immunotherapy is the most exciting advancement in cancer therapy. Similar to immune checkpoint blockade and chimeric antigen receptor T cell (CAR-T), bispecific antibody (BsAb) is attracting more and more attention as a novel strategy of antitumor immunotherapy. BsAb not only offers an effect...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607507/ https://www.ncbi.nlm.nih.gov/pubmed/28931402 http://dx.doi.org/10.1186/s13045-017-0522-z |
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author | Yu, Shengnan Li, Anping Liu, Qian Yuan, Xun Xu, Hanxiao Jiao, Dechao Pestell, Richard G. Han, Xinwei Wu, Kongming |
author_facet | Yu, Shengnan Li, Anping Liu, Qian Yuan, Xun Xu, Hanxiao Jiao, Dechao Pestell, Richard G. Han, Xinwei Wu, Kongming |
author_sort | Yu, Shengnan |
collection | PubMed |
description | Cancer immunotherapy is the most exciting advancement in cancer therapy. Similar to immune checkpoint blockade and chimeric antigen receptor T cell (CAR-T), bispecific antibody (BsAb) is attracting more and more attention as a novel strategy of antitumor immunotherapy. BsAb not only offers an effective linkage between therapeutics (e.g., immune effector cells, radionuclides) and targets (e.g., tumor cells) but also simultaneously blocks two different oncogenic mediators. In recent decades, a variety of BsAb formats have been generated. According to the structure of Fc domain, BsAb can be classified into two types: IgG-like format and Fc-free format. Among these formats, bispecific T cell engagers (BiTEs) and triomabs are commonly investigated. BsAb has achieved an exciting breakthrough in hematological malignancies and promising outcome in solid tumor as showed in various clinical trials. In this review, we focus on the preclinical experiments and clinical studies of epithelial cell adhesion molecule (EpCAM), human epidermal growth factor receptor (HER) family, carcinoembryonic antigen (CEA), and prostate-specific membrane antigen (PSMA) related BsAbs in solid tumors, as well as discuss the challenges and corresponding approaches in clinical application. |
format | Online Article Text |
id | pubmed-5607507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56075072017-09-24 Recent advances of bispecific antibodies in solid tumors Yu, Shengnan Li, Anping Liu, Qian Yuan, Xun Xu, Hanxiao Jiao, Dechao Pestell, Richard G. Han, Xinwei Wu, Kongming J Hematol Oncol Review Cancer immunotherapy is the most exciting advancement in cancer therapy. Similar to immune checkpoint blockade and chimeric antigen receptor T cell (CAR-T), bispecific antibody (BsAb) is attracting more and more attention as a novel strategy of antitumor immunotherapy. BsAb not only offers an effective linkage between therapeutics (e.g., immune effector cells, radionuclides) and targets (e.g., tumor cells) but also simultaneously blocks two different oncogenic mediators. In recent decades, a variety of BsAb formats have been generated. According to the structure of Fc domain, BsAb can be classified into two types: IgG-like format and Fc-free format. Among these formats, bispecific T cell engagers (BiTEs) and triomabs are commonly investigated. BsAb has achieved an exciting breakthrough in hematological malignancies and promising outcome in solid tumor as showed in various clinical trials. In this review, we focus on the preclinical experiments and clinical studies of epithelial cell adhesion molecule (EpCAM), human epidermal growth factor receptor (HER) family, carcinoembryonic antigen (CEA), and prostate-specific membrane antigen (PSMA) related BsAbs in solid tumors, as well as discuss the challenges and corresponding approaches in clinical application. BioMed Central 2017-09-20 /pmc/articles/PMC5607507/ /pubmed/28931402 http://dx.doi.org/10.1186/s13045-017-0522-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Yu, Shengnan Li, Anping Liu, Qian Yuan, Xun Xu, Hanxiao Jiao, Dechao Pestell, Richard G. Han, Xinwei Wu, Kongming Recent advances of bispecific antibodies in solid tumors |
title | Recent advances of bispecific antibodies in solid tumors |
title_full | Recent advances of bispecific antibodies in solid tumors |
title_fullStr | Recent advances of bispecific antibodies in solid tumors |
title_full_unstemmed | Recent advances of bispecific antibodies in solid tumors |
title_short | Recent advances of bispecific antibodies in solid tumors |
title_sort | recent advances of bispecific antibodies in solid tumors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607507/ https://www.ncbi.nlm.nih.gov/pubmed/28931402 http://dx.doi.org/10.1186/s13045-017-0522-z |
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