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CAR-T cell therapeutic avenue for fighting cardiac fibrosis: Roadblocks and perspectives.
Abdalla, Ahmed M E; Miao, Yu; Ahmed, Ahmed I M; Meng, Ning; Ouyang, Chenxi.
Afiliação
  • Abdalla AME; School of Biological Sciences and Technology, University of Jinan, Jinan, China.
  • Miao Y; Department of Biochemistry, College of Applied Science, University of Bahri, Khartoum, Sudan.
  • Ahmed AIM; NHC Key Laboratory of Diagnosis and Therapy of Gastrointestinal Tumor, Gansu Provincial Hospital, Lanzhou, China.
  • Meng N; Key Laboratory of Molecular Diagnostics and Precision Medicine for Surgical Oncology in Gansu Province, Gansu Provincial Hospital, Lanzhou, Gansu, China.
  • Ouyang C; Department of Biochemistry, College of Applied Science, University of Bahri, Khartoum, Sudan.
Cell Biochem Funct ; 42(2): e3955, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38379220
ABSTRACT
Heart diseases remain the primary cause of human mortality in the world. Although conventional therapeutic opportunities fail to halt or recover cardiac fibrosis, the promising clinical results and therapeutic efficacy of engineered chimeric antigen receptor (CART cell therapy show several advancements. However, the current models of CAR-T cells need further improvement since the T cells are associated with the triggering of excessive inflammatory cytokines that directly affect cardiac functions. Thus, the current study highlights the critical function of heart immune cells in tissue fibrosis and repair. The study also confirms CAR-T cell as an emerging therapeutic for treating cardiac fibrosis, explores the current roadblocks to CAR-T cell therapy, and considers future outlooks for research development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Antígenos Quiméricos Limite: Humans Idioma: En Revista: Cell Biochem Funct Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Antígenos Quiméricos Limite: Humans Idioma: En Revista: Cell Biochem Funct Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China