Kim Irene K, Bedi Damanpreet Singh, Denecke Christian, Ge Xupeng, Tullius Stefan G
Division of Transplant Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Transplantation. 2008 Oct 15;86(7):889-94. doi: 10.1097/TP.0b013e318186ac4a.
Until recently, research on transplantation rejection and tolerance has been directed toward deciphering the mechanisms of the adaptive immune system. However, the emergence that the innate immune system, the body's first-line defense against pathogens, has a strong influence on adaptive immunity has galvanized interest in elucidating the interplay between these two arms of the immune system. The discovery of Toll-like receptors and the characterization of the cellular mediators involved in innate immunity have provided growing evidence that innate immunity affects the adaptive immune response. Emerging evidence has also shown that early "danger signals"' associated with ischemia-reperfusion injury or brain death contribute to innate immune activation, promoting rejection, and inhibiting tolerance induction. In addition, nonspecific stimuli such as increased donor age or patient disease may also serve to exert a synergistic influence on innate immune activation. Ultimately, controlling the events in innate immune activation may help drive tolerance induction and reduce the rate of rejection.
直到最近,关于移植排斥和耐受的研究一直致力于破解适应性免疫系统的机制。然而,作为机体抵御病原体的第一道防线的先天免疫系统对适应性免疫有强大影响这一现象的出现,激发了人们对阐明免疫系统这两个分支之间相互作用的兴趣。Toll样受体的发现以及参与先天免疫的细胞介质的特性研究,提供了越来越多的证据表明先天免疫会影响适应性免疫反应。新出现的证据还表明,与缺血再灌注损伤或脑死亡相关的早期“危险信号”会导致先天免疫激活,促进排斥反应,并抑制耐受诱导。此外,诸如供体年龄增加或患者疾病等非特异性刺激也可能对先天免疫激活产生协同影响。最终,控制先天免疫激活中的各种事件可能有助于推动耐受诱导并降低排斥率。