Epstein Michelle M
Medical University of Vienna, Department of Dermatology, Lazarettgasse 19, Vienna A-1090, Austria.
Pharmacol Ther. 2006 Jan;109(1-2):107-36. doi: 10.1016/j.pharmthera.2005.06.006. Epub 2005 Aug 2.
Th2 memory cells play an important role in the pathogenesis of allergic asthma. Evidence from patients and experimental models indicates that memory Th2 cells reside in the lungs during disease remission and, upon allergen exposure, become activated effectors involved in disease exacerbation. The inhibition of memory Th2 cells or their effector functions in allergic asthma influence disease progression, suggesting their importance as therapeutic targets. They are allergen specific and can potentially be suppressed or eliminated using this specificity. They have distinct activation, differentiation, cell surface phenotype, migration capacity, and effector functions that can be targeted singularly or in combination. Furthermore, memory Th2 cells residing in the lungs can be treated locally. Capitalizing on these unique attributes is important for drug development for allergic asthma. The aim of this review is to present an overview of therapeutic strategies targeting Th2 memory cells in allergic asthma, emphasizing Th2 generation, differentiation, activation, migration, effector function, and survival.
Th2记忆细胞在过敏性哮喘的发病机制中起重要作用。来自患者和实验模型的证据表明,记忆性Th2细胞在疾病缓解期驻留在肺部,在接触过敏原后,成为参与疾病加重的活化效应细胞。抑制过敏性哮喘中的记忆性Th2细胞或其效应功能会影响疾病进展,表明它们作为治疗靶点的重要性。它们具有过敏原特异性,并且有可能利用这种特异性进行抑制或消除。它们具有独特的激活、分化、细胞表面表型、迁移能力和效应功能,可单独或联合靶向。此外,驻留在肺部的记忆性Th2细胞可以进行局部治疗。利用这些独特属性对于过敏性哮喘的药物开发很重要。本综述的目的是概述针对过敏性哮喘中Th2记忆细胞的治疗策略,重点关注Th2的产生、分化、激活、迁移、效应功能和存活。