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Development of Bispecific Antibody for Cancer Immunotherapy: Focus on T Cell Engaging Antibody.
Moon, Dain; Tae, Nara; Park, Yunji; Lee, Seung-Woo; Kim, Dae Hee.
Afiliação
  • Moon D; Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
  • Tae N; Global/Gangwon Innovative Biologics Regional Leading Research Center (GIB-RLRC), Kangwon National University, Chuncheon 24341, Korea.
  • Park Y; Pohang University of Science and Technology (POSTECH) Biotech Center, POSTECH, Pohang 37673, Korea.
  • Lee SW; Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.
  • Kim DH; College of Pharmacy, Kangwon National University, Chuncheon 24341, Korea.
Immune Netw ; 22(1): e4, 2022 Feb.
Article em En | MEDLINE | ID: mdl-35291652
ABSTRACT
In the era of immunotherapeutic control of cancers, many advances in biotechnology, especially in Ab engineering, have provided multiple new candidates as therapeutic immuno-oncology modalities. Bispecific Abs (BsAbs) that recognize 2 different antigens in one molecule are promising drug candidates and have inspired an upsurge in research in both academia and the pharmaceutical industry. Among several BsAbs, T cell engaging BsAb (TCEB), a new class of therapeutic agents designed to simultaneously bind to T cells and tumor cells via tumor cell specific antigens in immunotherapy, is the most promising BsAb. Herein, we are providing an overview of the current status of the development of TCEBs. The diverse formats and characteristics of TCEBs, in addition to the functional mechanisms of BsAbs are discussed. Several aspects of a new TCEB-Blinatumomab-are reviewed, including the current clinical data, challenges of patient treatment, drawbacks regarding toxicities, and resistance of TCEB therapy. Development of the next generation of TCEBs is also discussed in addition to the comparison of TCEB with current chimeric antigen receptor-T therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article