机构地区:[1]南京军区南京总医院肾脏科,国家肾脏疾病临床医学研究中心,全军肾脏病研究所,南京210016
出 处:《肾脏病与透析肾移植杂志》2015年第2期128-132,共5页Chinese Journal of Nephrology,Dialysis & Transplantation
基 金:国家科技支撑计划课题(2013BAI09B04)(2015BAI12B05);江苏省临床医学中心项目(BL2012007)
摘 要:目的:观察肾移植术后多瘤病毒相关性肾病(BKVAN)患者肾组织浸润细胞的变化,探讨其临床意义。方法:28例BKVAN患者作为研究对象(BKVAN组),选取26例急性排斥反应和19例常规活检患者作为对照组。比较BKVAN组与对照组肾组织中CD4^+、CD8^+、CD68^+、CD20^+细胞,白细胞介素2受体(IL-2R)的阳性表达及肾小管上皮细胞HLA-DR的阳性表达情况;根据血清肌酐(SCr)水平将BKVAN患者分为A1组11例(109.62<SCr≤219.23μmol/L)、A2组11例(219.23<SCr≤328.85μmol/L)和A3组6例(SCr>328.85μmol/L),观察不同SCr水平BKVAN患者移植肾组织中上述指标的变化。结果:BKVAN肾组织中CD4^+、CD8^+、CD68^+、CD20^+细胞、IL-2R的阳性表达较常规活检组均明显增加(P<0.01),而肾小管上皮细胞HLA-DR的阳性表达增加不明显;BKVAN组与急性排斥反应组相比,前者肾组织中B淋巴细胞浸润数量增加,但统计学差别不明显,而急性排斥反应组CD8^+细胞和肾小管上皮细胞HLA-DR的阳性表达显著增加(P<0.01)。随着SCr水平的升高,BKVAN患者移植肾组织中CD68^+细胞、IL-2R的阳性表达增加,其中A3组与A1组相比CD68^+细胞的浸润具有显著统计学差别(P<0.01)。结论:BKV诱发肾组织T淋巴细胞和B淋巴细胞活化,加重移植肾损害;与急性排斥相比BKVAN组受者肾组织中CD20^+细胞的浸润数量更多、肾小管上皮细胞HLA-DR阳性表达和CD8^+细胞明显减少。Objective:To investigate the immunohistological features of poiyomavirus type BK associated renal allograft nephropathy (BKVAN). Methodology: Seventy three patients with renal transplantation were selected in this retrospective study. They included 28 cases with BKVAN (BKVAN group), 26 cases with acute rejection (control group 1 ) and 19 cases with normal biopsy (control group 2). By immunohistochemistry ways, the difference of CD4, CDS, CD68, B lymphocyte and T lymphocyte interleukin-2 receptor (IL-2R) expressed in renal allograft biopsy and HLA-DR expressed in renal allograft tubular epithelial cell were observed among BKVAN group, control group 1 and control group 2. On the basis of serum creatinine(SCr) level, 28 patients with BKVAN were devided into group A1 ( 109. 62〈SCr≤219. 23 μmmol/L, n = 11 ), group A2 ( 219〈SCr≤328.85 μmmol/L, n = 11 ) and group A3 ( SCr〉328.85 μmmol/L, n = 6). The differences of IL-2R and HLA-DR were also observed among three groups . Results:The levels of CD4, CD8, CD68, B lymphocyte and T lymphocyte IL-2R were significantly increased in BKVAN group than those in the control group 2 (P〈0. 01 ), while the expression of HLA-DR in renal allograft tubular epithelial cell was not different. Although the number of B lymphocyte was arithmetically greater in BKVAN group than that in the control group 1, the difference was not statistically significant. The expression of HLA-DR in renal allograft tubular epithelial cell and the levels of CD8 were significantly increased in control group 1 compared to BKVAN group (P〈0. 01). With the elevated SCr level, the levels of CD68 and T lymphocyte IL-2R were moreincreased in BKVAN group, and there were significant differences between the group A3 and A1 (P〈0. 01). Conclusion: Renal allograft damage caused by BKVAN involved in both T and B lymphocyte mediated immune responses. BKVAN was characterized by the more B lymphocytes, not more expressed HLA-DR in renal allograft tubular e
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