Grattan C E, Walpole D, Francis D M, Niimi N, Dootson G, Edler S, Corbett M F, Barr R M
Department of Dermatology, Norfolk & Norwich Hospital, UK.
Clin Exp Allergy. 1997 Dec;27(12):1417-24. doi: 10.1046/j.1365-2222.1997.1630972.x.
Peripheral blood basophils are reduced in some chronic urticaria patients when counted with granule stains. Approximately 30% of patients with severe chronic urticaria have functional autoantibodies which release histamine from healthy donor basophils in vitro but the relationship between basophil numbers in vivo and serum histamine releasing activity has not been studied.
To determine the relationship between basophil numbers and serum basophil histamine releasing activity and to assess whether basophils are present, but undetectable, in peripheral blood with granule stains by using a new flow cytometric method based on surface immunophenotype.
Basophils were counted manually by a chamber method using a granule stain and by flow cytometry using dual staining with anti-IgE and anti-Fc epsilonRI in 25 chronic idiopathic urticaria patients and 25 healthy controls. Serum histamine releasing activity was assessed on healthy donor basophils in vitro and by the weal response to autologous serum skin testing in vivo (patients only).
Basophils were significantly reduced in chronic urticaria by manual counting and flow cytometry. A subgroup of seven patients with in vitro histamine releasing activity showed a marked reduction or absence of basophils by both methods. There were no obvious distinguishing clinical characteristics between these patients and the others; six of them showed positive autologous serum skin-test responses. On comparing the two methods, the manual basophil counts were generally lower than flow cytometric counts. Agreement over the full range of values was not strong and therefore counts obtained by the two methods are not directly interchangeable.
Basopenia in chronic idiopathic urticaria is associated with serum basophil histamine releasing activity in a subgroup of patients. The lack of granule and surface immunophenotype staining suggests a reduction in numbers rather than an inability to detect circulating degranulated cells by conventional counting methods.
使用颗粒染色计数时,一些慢性荨麻疹患者的外周血嗜碱性粒细胞数量减少。约30%的严重慢性荨麻疹患者具有功能性自身抗体,可在体外使健康供体嗜碱性粒细胞释放组胺,但体内嗜碱性粒细胞数量与血清组胺释放活性之间的关系尚未得到研究。
通过基于表面免疫表型的新型流式细胞术方法,确定嗜碱性粒细胞数量与血清嗜碱性粒细胞组胺释放活性之间的关系,并评估外周血中是否存在用颗粒染色无法检测到的嗜碱性粒细胞。
采用颗粒染色通过计数板法手动计数嗜碱性粒细胞,并通过抗IgE和抗FcεRI双重染色的流式细胞术对25例慢性特发性荨麻疹患者和25例健康对照进行计数。体外评估健康供体嗜碱性粒细胞的血清组胺释放活性,并在体内(仅针对患者)通过自体血清皮肤试验的风团反应进行评估。
通过手动计数和流式细胞术,慢性荨麻疹患者的嗜碱性粒细胞显著减少。7例具有体外组胺释放活性的患者亚组,两种方法均显示嗜碱性粒细胞明显减少或缺失。这些患者与其他患者之间没有明显的临床特征差异;其中6例自体血清皮肤试验反应呈阳性。比较两种方法,手动嗜碱性粒细胞计数通常低于流式细胞术计数。在整个数值范围内的一致性不强,因此两种方法获得的计数不能直接互换。
在一部分慢性特发性荨麻疹患者中,嗜碱性粒细胞减少与血清嗜碱性粒细胞组胺释放活性相关。缺乏颗粒和表面免疫表型染色提示细胞数量减少,而非传统计数方法无法检测到循环中的脱颗粒细胞。