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The role of TIM-3 in sepsis: a promising target for immunotherapy?
Wang, Changli; Liu, Jinhai; Wu, Qi; Wang, Zhi; Hu, Baoji; Bo, Lulong.
Afiliação
  • Wang C; Faculty of Anesthesiology, Changhai Hospital, Naval Medical University, Shanghai, China.
  • Liu J; Faculty of Anesthesiology, Changhai Hospital, Naval Medical University, Shanghai, China.
  • Wu Q; Faculty of Anesthesiology, Changhai Hospital, Naval Medical University, Shanghai, China.
  • Wang Z; Faculty of Anesthesiology, Changhai Hospital, Naval Medical University, Shanghai, China.
  • Hu B; Department of Anesthesiology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
  • Bo L; Faculty of Anesthesiology, Changhai Hospital, Naval Medical University, Shanghai, China.
Front Immunol ; 15: 1328667, 2024.
Article em En | MEDLINE | ID: mdl-38576606
ABSTRACT
Sepsis remains a significant cause of mortality and morbidity worldwide, with limited effective treatment options. The T-cell immunoglobulin and mucin domain-containing molecule 3 (TIM-3) has emerged as a potential therapeutic target in various immune-related disorders. This narrative review aims to explore the role of TIM-3 in sepsis and evaluate its potential as a promising target for immunotherapy. We discuss the dynamic expression patterns of TIM-3 during sepsis and its involvement in regulating immune responses. Furthermore, we examine the preclinical studies investigating the regulation of TIM-3 signaling pathways in septic models, highlighting the potential therapeutic benefits and challenges associated with targeting TIM-3. Overall, this review emphasizes the importance of TIM-3 in sepsis pathogenesis and underscores the promising prospects of TIM-3-based immunotherapy as a potential strategy to combat this life-threatening condition.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sepse / Receptor Celular 2 do Vírus da Hepatite A Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sepse / Receptor Celular 2 do Vírus da Hepatite A Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article