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阿尔茨海默病及一些相关病症的免疫病理学

The immunopathology of Alzheimer's disease and some related disorders.

作者信息

Kalaria R N

机构信息

Department of Neurology, Case Western Reserve University School of Medicine, Cleveland, OH 44106.

出版信息

Brain Pathol. 1993 Oct;3(4):333-47. doi: 10.1111/j.1750-3639.1993.tb00761.x.

Abstract

Current evidence clearly indicates that elements of the immune system are involved in the pathogenesis of the principal lesions characterizing Alzheimer's disease (AD). Findings are in accord with features associated with both the innate and adaptive immune mechanisms involved in a predominantly local inflammatory response within the parenchyma. Many of the features are unique to AD, presumably related to the unusual properties of beta amyloid protein. Remarkably, the brain holds the capacity to produce almost all the immune system mediators which largely seem to be generated by glia comprising both astrocytes and microglia. While a variety of humoral mediators including classical acute phase proteins (and serpins) are increased and released, the complement seems most intrinsically involved. The cellular response is elaborated by microglia which seem the main immunocompetent cells partaking in the response. These appear to function as pluripotent macrophages expressing both classes of MHC antigens. Further characterization of this interesting response to cerebral amyloidosis will be challenging.

摘要

目前的证据清楚地表明,免疫系统的元素参与了阿尔茨海默病(AD)主要病变的发病机制。研究结果与涉及实质内主要局部炎症反应的先天免疫和适应性免疫机制相关的特征一致。许多特征是AD所特有的,可能与β淀粉样蛋白的异常特性有关。值得注意的是,大脑有能力产生几乎所有的免疫系统介质,这些介质似乎主要由包括星形胶质细胞和小胶质细胞在内的胶质细胞产生。虽然包括经典急性期蛋白(和丝氨酸蛋白酶抑制剂)在内的多种体液介质增加并释放,但补体似乎最内在地参与其中。细胞反应由小胶质细胞阐述,小胶质细胞似乎是参与反应的主要免疫活性细胞。这些细胞似乎作为表达两类MHC抗原的多能巨噬细胞发挥作用。对这种有趣的脑淀粉样变性反应的进一步表征将具有挑战性。

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