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引用次数: 0
摘要
成熟的幼稚 CD4 SP T 细胞从人类胸腺向外周移出的情况尚未完全清楚,尽管阐明支配 T 细胞移出的机制对于理解基础免疫学和艾滋病病毒感染等疾病的免疫反应至关重要。最近的研究揭示了鞘氨醇-1-磷酸(S1P)及其受体在多个领域的需求,包括成熟的幼稚 T 细胞从小鼠胸腺排出。我们正在研究人类胸腺中这种新的必要T细胞排出受体的表达和功能,并对在感染性疾病中观察到的这种受体的表达和功能变化进行定性。为了完成这项工作,我们使用了本文中评述的各种人源化小鼠模型。未来在T细胞出路领域的工作,尤其是与S1P受体有关的工作,将推动基础T细胞免疫学和免疫病理学领域的发展,并为探索新型疗法开辟新的途径。
Human T-Cell Development and Thymic Egress: An Infectious Disease Perspective.
Emigration of mature naïve CD4 SP T cells from the human thymus to the periphery is not fully understood, although elucidation of the mechanisms that govern egress of T cells is crucial to understanding both basic immunology and the immune response in diseases such as HIV infection. Recent work has brought to light the requirement for sphingosine-1-phosphate (S1P) and its receptors in a variety of fields including mature naïve T-cell egress from the thymus of mice. We are examining the expression and function of this novel requisite T-cell egress receptor within the human thymus, characterizing changes observed in the expression and function of this receptor in infectious diseases. To perform this work, we use a variety of humanized murine models reviewed in this article. Future work in the field of T-cell egress, especially as it pertains to S1P receptors, should advance the fields of basic T-cell immunology and immunopathology and open new avenues for exploration into novel therapeutics.