Sohani Zahra N, Strinich Tara X, Watson Brittany, Smith Steven G, Torek Abbey, Howie Karen J, Gauvreau Gail M
Department of Medicine, McMaster University, Hamilton, ON, Canada.
J Asthma. 2011 Nov;48(9):952-6. doi: 10.3109/02770903.2011.617477.
Induced sputum is used to assess markers of inflammation in asthmatic individuals, and sputum cell differential counts provide an outcome to evaluate the presence, type, and degree of inflammation in the airways. Contamination of sputum slides with squamous epithelial cells (SECs) has been reported to adversely affect the reproducibility of sputum cell differential counts; however, this has not been studied in a controlled manner. Excluding sputum slides because of excessive squamous cell contamination can be problematic resulting in under-powering of studies. The aim of this study is to evaluate the effect of SEC contamination and cell dispersion on the reproducibility of differential counts of sputum cells prepared on glass slides.
A total of 33 sputum samples were induced from 11 subjects with mild asthma under baseline conditions and following an allergen inhalation challenge. Mucoid and salivary portions of each sample were divided and processed in parallel. To evaluate the effect of increasing the proportion of SEC and to evaluate the effect of increasing the number of leukocytes per high power field (HPF), four slides with varying leukocyte numbers and SEC percentages were prepared from each sample by combining and adjusting the volume of cell suspensions derived from mucous and saliva. The four slides were prepared to fall in the following categories: (A) 50 cells/HPF and <20% SEC; (B) 50 cells/HPF and >20% SEC; (C) 100 cells/HPF and <20% SEC; and (D) 100 cells/HPF and >20% SEC. All slides were blinded and counted twice by an experienced observer, and twice by an inexperienced observer.
The differential cell counts for eosinophils, macrophages, and neutrophils were highly reproducible under all conditions when enumerated by an experienced observer (ICC > 0.9), and furthermore, SEC contamination did not affect ICC when differential counts were enumerated by an inexperienced observer (ICC > 0.8).
Our results demonstrate that slides containing SECs, up to 40% in this study, have reproducible differential cell counts.
诱导痰用于评估哮喘患者的炎症标志物,痰细胞分类计数可作为评估气道炎症的存在、类型和程度的一项指标。据报道,痰涂片被鳞状上皮细胞(SEC)污染会对痰细胞分类计数的可重复性产生不利影响;然而,尚未对此进行对照研究。由于鳞状细胞污染过多而排除痰涂片可能会产生问题,导致研究效能不足。本研究的目的是评估SEC污染和细胞分散对玻片上制备的痰细胞分类计数可重复性的影响。
在基线条件下以及过敏原吸入激发后,从11名轻度哮喘患者中总共诱导出33份痰样本。将每个样本的黏液样和唾液样部分分开并并行处理。为了评估增加SEC比例的影响以及评估每高倍视野(HPF)白细胞数量增加的影响,通过合并和调整来自黏液和唾液的细胞悬液体积,从每个样本制备了四张白细胞数量和SEC百分比不同的玻片。制备的四张玻片分为以下几类:(A)50个细胞/HPF且SEC<20%;(B)50个细胞/HPF且SEC>20%;(C)100个细胞/HPF且SEC<20%;(D)100个细胞/HPF且SEC>20%。所有玻片均进行盲法计数,由一名经验丰富的观察者计数两次,一名经验不足的观察者也计数两次。
当由经验丰富的观察者计数时,在所有条件下嗜酸性粒细胞、巨噬细胞和中性粒细胞的分类细胞计数具有高度可重复性(组内相关系数>0.9),此外,当由经验不足的观察者进行分类计数时,SEC污染不影响组内相关系数(组内相关系数>0.8)。
我们的结果表明,本研究中含有高达40% SEC的玻片具有可重复的分类细胞计数。