Your browser doesn't support javascript.
loading
Potential biomarkers: Identifying powerful tumor specific T cells in adoptive cellular therapy.
Ge, Wu; Dong, Yuqian; Deng, Yao; Chen, Lujuan; Chen, Juan; Liu, Muqi; Wu, Jianmin; Wang, Wei; Ma, Xiaoqian.
Afiliação
  • Ge W; Cell Transplantation and Gene Therapy Institute, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Dong Y; Department of Radiology, The Third Xiangya Hospital of Central South University, Changsha, China.
  • Deng Y; Department of Radiology, The Third Xiangya Hospital of Central South University, Changsha, China.
  • Chen L; Department of Radiology, The Third Xiangya Hospital of Central South University, Changsha, China.
  • Chen J; Department of Radiology, The Third Xiangya Hospital of Central South University, Changsha, China.
  • Liu M; Department of Radiology, The Third Xiangya Hospital of Central South University, Changsha, China.
  • Wu J; Department of Radiology, The Third Xiangya Hospital of Central South University, Changsha, China.
  • Wang W; Department of Radiology, The Third Xiangya Hospital of Central South University, Changsha, China.
  • Ma X; Cell Transplantation and Gene Therapy Institute, The Third Xiangya Hospital, Central South University, Changsha, China.
Front Immunol ; 13: 1003626, 2022.
Article em En | MEDLINE | ID: mdl-36451828
Tumor-specific T cells (TSTs) are essential components for the success of personalized tumor-infiltrating lymphocyte (TIL)-based adoptive cellular therapy (ACT). Therefore, the selection of a common biomarker for screening TSTs in different tumor types, followed by ex vivo expansion to clinical number levels can generate the greatest therapeutic effect. However, studies on shared biomarkers for TSTs have not been realized yet. The present review summarizes the similarities and differences of a number of biomarkers for TSTs in several tumor types studied in the last 5 years, and the advantages of combining biomarkers. In addition, the review discusses the possible shortcomings of current biomarkers and highlights strategies to identify TSTs accurately using intercellular interactions. Finally, the development of TSTs in personalized TIL-based ACT for broader clinical applications is explored.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article