恶性胸腔积液
医学
胸腔积液
免疫系统
人口
细胞因子
细胞
癌症研究
生物
免疫学
病理
内科学
遗传学
环境卫生
作者
Feng‐Shuang Yi,Kan Zhai,Huan‐Zhong Shi
标识
DOI:10.1016/j.canlet.2020.12.016
摘要
Malignant pleural effusion (MPE) is a frequent complication of malignancies and poses a clinical problem. CD4+ T lymphocytes are the most frequent cell population in MPE. Traditionally, CD4+ T cells are classified into two subsets based on cytokine production profiles, type 1 (Th1) and type 2 (Th2) helper T cells, which exhibit distinct functions. Recently, other T-cell subsets have been added to the Th-cell "portfolio", including regulatory T, Th17, Th9, and Th22 cells. The current review focuses on summarizing the Th-cell phenotypic characteristics, mechanism of Th-cell differentiation, and their pleural space recruitment, based on recent research. We also describe the interplay in MPE among different Th cells, as well as Th cells and lung cancer cells or mesothelial cells. Future research should expand the landscape map of human MPE immune cells, explore the immuno-regulation of B cells, and investigate the communication between macrophages and Th cells in MPE, which may facilitate meaningful advancements in the diagnoses and therapeutics of MPE.
科研通智能强力驱动
Strongly Powered by AbleSci AI