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Glomerular chemokine expression and the effect of steroid and cyclophosphamide pulse therapy in human crescentic glomerulonephritis

机译:肾小球趋化因子的表达以及类固醇和环磷酰胺脉冲疗法在人新月型肾小球肾炎中的作用

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Objective To study glomerular expression of C-C chemokines, monocyte chemoattractant protein-1 (MCP-1), macrophage inflammatory protein-1α and β (MIP-1α, MIP-1β) and the effect of steroid and cyclophosphamide (CTX) intermittent intravenous pulse therapy on expression in patients with crescentic glomerulonephritis (CGN) to further investigate the underlying mechanism of the treatment. Methods Twelve patients with initial biopsy-proven CGN_2, 6 with lupus nephritis (lupus-CGN, LN-CGN) and 6 with vasculitis, (vasculitis-CGN, V-CGN) were enrolled in this study. They underwent an initial biopsy before steroid and CTX intermittent intravenous pulse therapy and were biopsied again one to three months later. Expression of MCP-1, MIP-1α, MIP-1?, and CD68 in glomeruli with cellular and fibrocellular crescents were examined by immunohistochemical analysis in serial sections of renal biopsies. The effect of the pulse therapy on histopathological changes was also observed. Results Although steroid and CTX intermittent intravenous pulse therapy markedly reduced the degree of glomerular crescent formation both in LN-CGN and V-CGN, the effect of the therapy on glomerular chemokine expression was significantly different between LN-CGN and V-CGN. It was found that steroid and CTX intermittent intravenous pulse therapy reduced the expression of CD68, MCP-1, and MIP-1α, but had no effect on MIP-1β in glomeruli with cellular crescents of patients with LN-CGN. In patients with V-CGN, the therapy also reduced the expression of CD68, but had no effect on MCP-1, MIP-1α, and MIP-1β in glomeruli with cellular crescents. It was noted that the degree of glomerulosclerosis and tubular interstitial fibrosis increased more significantly at the second biopsy in V-CGN as compared to LN-CGN. Conclusions The efficacy of steroid and CTX intermittent intravenous pulse therapy in CGN might be affected by reduction of glomerular chemokine expression. The different changes in glomerular expression of MCP-1 and MIP-1α in patients with LN-CGN and V-CGN after pulse therapy may correlate to different responses to treatment and prognosis.
机译:目的研究CC趋化因子,单核细胞趋化蛋白-1(MCP-1),巨噬细胞炎性蛋白-1α和β(MIP-1α,MIP-1β)的肾小球表达以及类固醇和环磷酰胺(CTX)间歇静脉脉冲治疗的作用对新月型肾小球肾炎(CGN)患者中的表达进行研究,以进一步研究治疗的潜在机制。方法招募了12例经初步活检证实的CGN_2患者,6例狼疮性肾炎(lupus-CGN,LN-CGN)和6例血管炎(血管炎-CGN,V-CGN)。他们在接受类固醇和CTX间歇性静脉脉冲治疗之前进行了首次活检,并在一到三个月后再次进行了活检。通过免疫组织化学分析在肾活检的连续切片中检查了MCP-1,MIP-1α,MIP-1α和CD68在具有细胞和纤维细胞新月的肾小球中的表达。还观察到脉冲疗法对组织病理学改变的影响。结果尽管类固醇和CTX间歇性静脉内脉冲治疗显着降低了LN-CGN和V-CGN的肾小球新月形形成程度,但该疗法对LN-CGN和V-CGN的肾小球趋化因子表达的影响显着不同。研究发现,类固醇和CTX间歇性静脉内脉冲疗法可降低CD68,MCP-1和MIP-1α的表达,但对LN-CGN患者的新月形肾小球中MIP-1β无效。在V-CGN患者中,该疗法还降低了CD68的表达,但对新月型肾小球的MCP-1,MIP-1α和MIP-1β没有影响。值得注意的是,与LN-CGN相比,V-CGN第二次活检时肾小球硬化和肾小管间质纤维化的程度明显增加。结论降低肾小球趋化因子表达可能会影响类固醇和CTX间歇静脉脉冲治疗CGN的疗效。 LN-CGN和V-CGN患者脉冲治疗后MCP-1和MIP-1α肾小球表达的不同变化可能与对治疗和预后的不同反应有关。

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