Józefowski Szczepan
Katedra i Zakład Immunologii, Uniwersytet Jagielloński, Collegium Medicum, ul. Czysta 18, 31-121 Kraków.
Postepy Hig Med Dosw (Online). 2012 Feb 29;66:120-31. doi: 10.5604/17322693.984080.
Recognition of pathogens by innate immune cells is mediated by pattern recognition receptors (PRR), which include the class A scavenger receptors (SR), SR-A/CD204 and MARCO. It seems that in addition to activating innate immune responses, phagocytosis and inflammation, this initial, PRR-mediated recognition also determines polarization of adaptive immune responses (Th1, Th2, Th17 or Treg). It has been demonstrated that class A SR are major PRR mediating opsonin-independent phagocytosis. SR-A- or MARCO-deficient mice exhibit impaired ability to control bacterial infections, resulting in increased mortality. Our results suggest that in addition to impaired bacterial destruction by macrophages, dysregulation of immune responses may contribute to defective antibacterial defense in class A SR-deficient mice. Using specific receptor ligation with antibodies, we showed that SR-A and MARCO regulate in an opposite manner production of IL-12 in macrophages, the cytokine playing a crucial role in Th1/Th2 polarization of adaptive immune responses. Together with the observation that expression of MARCO is increased by different Th1-polarizing factors and decreased by Th2-polarizing factors, these results suggest that changes in relative expression levels of SR-A and MARCO may be a mechanism of sustained polarization of adaptive immune responses.
天然免疫细胞对病原体的识别由模式识别受体(PRR)介导,其中包括A类清道夫受体(SR),即SR-A/CD204和MARCO。除了激活天然免疫反应、吞噬作用和炎症外,这种由PRR介导的初始识别似乎还决定了适应性免疫反应(Th1、Th2、Th17或Treg)的极化。已证明A类SR是介导不依赖调理素吞噬作用的主要PRR。缺乏SR-A或MARCO的小鼠控制细菌感染的能力受损,导致死亡率增加。我们的结果表明,除了巨噬细胞对细菌的破坏受损外,免疫反应失调可能导致A类SR缺陷小鼠的抗菌防御功能缺陷。通过用抗体进行特异性受体连接,我们发现SR-A和MARCO以相反的方式调节巨噬细胞中IL-12的产生,IL-12是在适应性免疫反应的Th1/Th2极化中起关键作用的细胞因子。结合MARCO的表达在不同的Th1极化因子作用下增加而在Th2极化因子作用下减少这一观察结果,这些结果表明SR-A和MARCO相对表达水平的变化可能是适应性免疫反应持续极化的一种机制。