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首页> 外文期刊>Academic Journal of Xian Jiaotong University >THE STUDY ON RELATION BETWEEN CD1A~+ CELLS AND INFILTRATIVE CD3~+ AND CD8+ CELLS IN RENAL TISSUE OF GLOMERULONEPHRITIS
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THE STUDY ON RELATION BETWEEN CD1A~+ CELLS AND INFILTRATIVE CD3~+ AND CD8+ CELLS IN RENAL TISSUE OF GLOMERULONEPHRITIS

机译:肾盂球菌肾组织中CD1A〜+细胞与侵袭性CD3〜+和CD8 +细胞关系的研究

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摘要

Objective To discuss the role of dendritic cells (DCs) in cellular immunity pathogenesis of glomerulonephritis (GN). Methods 114 patients with GN were selected randomly and divided into two groups, primary GN (pGN) and secondry GN (sGN). CD1a~+, CD3~+ and CD8~+ ceils in bioptic renal tissues were examined immunohistochemically. The distribution of CD1a+ cells and the infiltration of CD3+ and CD8+ cells in renal tissues were observed. Results There was no significant difference of CD1a~+, CD3+ , and CD8+ cells between pGN and sGN group (P>0. 05). CD1a+ cells had significant positive correlation with the infiltrative CD3+ and CD8+ cells, respectively (P<0. 01). The infiltrative CD3+ cells had significant positive correlation with the CD8+ cells in the same area, respectively (P<0. 01). CD1a+ cells, CD3+ cells infiltrating in both glomeruli and renal interstitial tissues, and CD8+ cells only infiltrating in renal interstitial tissues, all of them had significant positive correlation with the degree of glomerular proliferation, respectively (P<0. 05). The infiltrative CD3~+ and CD8~+ cells in renal interstitial tissues had significant positive correlation with the degree of glomerular sclerosis and the lesion degree of renal tubule and interstitial, respectively (P<0. 05). There were significant positive correlation between CD1a~+ cells and the lesion degree of renal interstitial (P<0. 05). Conclusion DCs could activate T lymphocyte by presenting antigen, then the activated T lymphocyte participate in the pathogenesis of GN through releasing cytokine and/or directly damaging the renal tubule and interstitial, which produce more serious glomerular lesion.
机译:目的探讨树突状细胞(DCs)在肾小球肾炎(GN)细胞免疫发病机制中的作用。方法随机选择114例GN患者,分为原发性GN(pGN)和次生性GN(sGN)两类。免疫组织化学检查肾活检组织中CD1a〜+,CD3〜+和CD8〜+细胞。观察肾组织中CD1a +细胞的分布以及CD3 +和CD8 +细胞的浸润情况。结果pGN组和sGN组之间CD1a〜+,CD3 +和CD8 +细胞差异无统计学意义(P> 0。05)。 CD1a +细胞分别与浸润性CD3 +细胞和CD8 +细胞呈显着正相关(P <0.01)。浸润性CD3 +细胞分别与同一区域的CD8 +细胞具有显着正相关(P <0.01)。在肾小球和肾间质组织中均浸润的CD1a +细胞,CD3 +细胞和仅在肾间质组织中浸润的CD8 +细胞分别与肾小球增生程度显着正相关(P <0。05)。肾间质组织中浸润性CD3〜+和CD8〜+细胞分别与肾小球硬化程度,肾小管和间质病变程度呈显着正相关(P <0。05)。 CD1a〜+细胞与肾间质病变程度呈显着正相关(P <0。05)。结论DCs可通过呈递抗原来激活T淋巴细胞,然后激活的T淋巴细胞通过释放细胞因子和/或直接破坏肾小管和间质而参与GN的发病过程,从而产生更严重的肾小球病变。

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