McGeer E G, McGeer P L
Kinsmen Laboratory of Neurological Research, University of British Columbia, 2255 Wesbrook Mall, Vancouver, B.C., V6T 1Z3, Canada.
Curr Pharm Des. 1999 Oct;5(10):821-36.
Immunohistochemical studies suggested the existence of a chronic inflammatory condition in affected regions of the brain in Alzheimer disease (AD). Since inflammation can be damaging to host tissue, it was hypothesized that antiinflammatory drugs might inhibit both the onset and the progression of AD. This hypothesis is supported by a number of epidemiological studies suggesting that the prevalence of AD in persons is reduced by 40 - 50% in persons using antiinflammatory drugs. In one small pilot trial in early AD, the nonsteroidal antiinflammatory drug indomethacin appeared to halt the progressive memory loss. Immunohistochemical and molecular biological studies on immune system components in AD brain are revealing the complexities of the innate immune reaction. This very complexity may offer points of therapeutic intervention for new types of antiinflammatory agents. The complement system, microglia and cytokines are key components. This review summarizes the present state of knowledge on the immune system elements found in AD brain.
免疫组化研究表明,阿尔茨海默病(AD)患者大脑的病变区域存在慢性炎症状态。由于炎症会对宿主组织造成损害,因此有人推测抗炎药物可能会抑制AD的发病和进展。这一假说得到了多项流行病学研究的支持,这些研究表明,使用抗炎药物的人群中AD的患病率降低了40%-50%。在一项针对早期AD的小型试点试验中,非甾体抗炎药吲哚美辛似乎能够阻止进行性记忆丧失。对AD大脑中免疫系统成分的免疫组化和分子生物学研究正在揭示先天免疫反应的复杂性。这种复杂性可能为新型抗炎药物提供治疗干预点。补体系统、小胶质细胞和细胞因子是关键成分。本综述总结了目前关于AD大脑中发现的免疫系统元素的知识现状。