Liu G, Wu C, Wu Y, Zhao Y
Transplantation Biology Research Division, State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Scand J Immunol. 2006 Jul;64(1):1-9. doi: 10.1111/j.1365-3083.2006.01771.x.
The termination of the apoptotic programme occurs in most cases via recognition and clearance by phagocytes, especially the professional phagocytes, such as macrophages and immature dendritic cells. Engulfed cells do not simply disappear from the midst of living tissues. The fine-defined presentation of yielded self-antigens to T cells is a central event in the induction or the maintenance of the peripheral immune tolerance to self. Conversely, abnormality in this pathway may contribute to the pathogenesis of systemic and organ-specific autoimmune diseases. We herein reviewed the relationship between phagocytosis of apoptotic cells and immune regulation, especially the effects of engulfed apoptotic cells on immune tolerance and autoimmune diseases.
在大多数情况下,凋亡程序的终止是通过吞噬细胞,尤其是专业吞噬细胞,如巨噬细胞和未成熟树突状细胞的识别和清除来实现的。被吞噬的细胞不会简单地从活组织中消失。产生的自身抗原向T细胞的精细呈递是诱导或维持外周自身免疫耐受的核心事件。相反,该途径的异常可能导致全身性和器官特异性自身免疫性疾病的发病机制。我们在此综述了凋亡细胞吞噬与免疫调节之间的关系,特别是被吞噬的凋亡细胞对免疫耐受和自身免疫性疾病的影响。