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人MPO-ANCA相关性肾小球肾炎中MPO、IgG和C3在肾小球中的免疫病理共定位。

Immunopathologic co-localization of MPO, IgG, and C3 in glomeruli in human MPO-ANCA-associated glomerulonephritis.

作者信息

Kawashima Soko, Arimura Yoshihiro, Sano Katsuko, Kudo Akihiko, Komagata Yoshinori, Kaname Shinya, Kawakami Hayato, Yamada Akira

机构信息

First Department of Internal Medicine, Kyorin University School of Medicine, Tokyo, Japan.

出版信息

Clin Nephrol. 2013 Apr;79(4):292-301. doi: 10.5414/cn107675.

Abstract

Myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA)- associated glomerulonephritis (GN) is characterized by pauci-immune necrotizing glomerulonephritis(NGN). Although it has been thought that MPO-ANCA is involved in the pathogenesis of capillary injuries in NGN via activation of neutrophils, recent studies suggest a possible role of other factors such as immunoglobulins precipitated on the glomeruli. Here we performed a pathological study investigating a relationship of deposition of MPO, IgG, complements with regard to MPO-positive cells and glomerular capillaries in human MPO-ANCA-associated GN. Renal specimen including 317 glomeruli obtained from 20 patients with MPOANCA- associated GN were analyzed. All of the specimens showed significant focal segmental deposition of IgG. There was a significant glomerular infiltration of MPO-positive cells along with deposition of extracellular MPO in the active lesions of segmental and global NCG, with CD34 staining being decreased in the adjacent areas. IgG deposits were almost colocalized with C3 and partly with MPO, which are also associated with a decrease in CD34 staining, suggesting that immune complex formation and the resultant capillary injuries. Actually occurred, the colocalization of MPO, IgG and C3 was seen only in the glomerular lesions with low severity and activity. These results suggest that not only MPO itself released from the neutrophils but also immune complexes composed of MPO and anti-MPO antibody may play some pathogenetic roles for the glomerular injuries especially in the early phase of human MPO-ANCA-associated GN.

摘要

髓过氧化物酶抗中性粒细胞胞浆抗体(MPO-ANCA)相关肾小球肾炎(GN)的特征是寡免疫坏死性肾小球肾炎(NGN)。尽管一直认为MPO-ANCA通过激活中性粒细胞参与NGN中毛细血管损伤的发病机制,但最近的研究表明其他因素可能发挥作用,如肾小球上沉淀的免疫球蛋白。在此,我们进行了一项病理学研究,调查人MPO-ANCA相关GN中MPO、IgG、补体的沉积与MPO阳性细胞和肾小球毛细血管之间的关系。分析了从20例MPO-ANCA相关GN患者获取的包括317个肾小球的肾标本。所有标本均显示IgG有显著的局灶节段性沉积。在节段性和球性NCG的活动性病变中,MPO阳性细胞有显著的肾小球浸润,同时细胞外MPO沉积,相邻区域CD34染色减少。IgG沉积物几乎与C3共定位,部分与MPO共定位,这也与CD34染色减少有关,提示免疫复合物形成及由此导致的毛细血管损伤实际发生,MPO、IgG和C3的共定位仅在低严重程度和低活性的肾小球病变中可见。这些结果表明,不仅从中性粒细胞释放的MPO本身,而且由MPO和抗MPO抗体组成的免疫复合物可能在肾小球损伤中发挥某些致病作用,尤其是在人MPO-ANCA相关GN的早期阶段。

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