Furness P N, Rogers-Wheatley L, Harris K P
Department of Pathology, Leicester General Hospital.
J Clin Pathol. 1997 Feb;50(2):118-22. doi: 10.1136/jcp.50.2.118.
To develop and validate a rapid and economical semiautomated approach to the measurement of immunostainable tissue components which is applicable to routine diagnostic practice. To apply this approach to the measurement of macrophages in renal biopsy specimens in nephrotic states, as protein in the renal tubules may induce macrophage infiltration, and the morphology of macrophages in tissue sections does not lend itself to cell counting.
Macrophages were identified by immunostaining with a pan-macrophage marker, followed by digital image capture and analysis using a macro procedure written for the freeware image analysis program NIH-Image.
The method was rapid, robust and accurate to within the limits imposed by sampling error inherent in the use of small needle biopsy specimens. Very few macrophages are found in normal kidney (mean volume fraction (+/- 95% confidence limits) 0.04% (0.02%)) but infiltration of macrophages was detected in minimal change nephropathy (0.29% (0.12%)) and in membranous glomerulonephritis (0.42% (0.11%)). A statistically significant correlation was found between macrophage volume fraction and weight of proteinuria in minimal change nephropathy but not in membranous glomerulonephritis. Correlations were found in both diseases between macrophage volume fraction and serum creatinine at time of biopsy.
The equipment is inexpensive and measurement takes less than one minute per biopsy specimen. The results indicate that macrophage infiltration is part of the pathological process in minimal change nephropathy and membranous glomerulonephritis. The correlation with creatinine at time of biopsy suggests that renal impairment in minimal change nephropathy may result from infiltration by immunologically active cells and not merely from haemodynamic changes in nephrons. However, the correlation is not close, indicating that the relation between macrophage infiltration and disease severity is not a simple one.
开发并验证一种快速且经济的半自动化方法,用于测量可免疫染色的组织成分,该方法适用于常规诊断实践。将此方法应用于肾病状态下肾活检标本中巨噬细胞的测量,因为肾小管中的蛋白质可能诱导巨噬细胞浸润,且组织切片中巨噬细胞的形态不利于细胞计数。
通过用全巨噬细胞标志物进行免疫染色来识别巨噬细胞,随后使用为免费软件图像分析程序NIH-Image编写的宏程序进行数字图像捕获和分析。
该方法快速、稳健且准确,在使用小针活检标本固有的抽样误差范围内。正常肾脏中发现的巨噬细胞极少(平均体积分数(±95%置信限)为0.04%(0.02%)),但在微小病变性肾病(0.29%(0.12%))和膜性肾小球肾炎(0.42%(0.11%))中检测到巨噬细胞浸润。在微小病变性肾病中,巨噬细胞体积分数与蛋白尿重量之间存在统计学显著相关性,但在膜性肾小球肾炎中未发现。在两种疾病中,活检时巨噬细胞体积分数与血清肌酐之间均存在相关性。
该设备价格低廉,每个活检标本的测量时间不到一分钟。结果表明,巨噬细胞浸润是微小病变性肾病和膜性肾小球肾炎病理过程的一部分。活检时与肌酐的相关性表明,微小病变性肾病中的肾功能损害可能是由免疫活性细胞浸润所致,而不仅仅是由于肾单位的血流动力学变化。然而,这种相关性并不紧密,表明巨噬细胞浸润与疾病严重程度之间的关系并非简单的关系。