首页> 外文期刊>Journal of Clinical Microbiology >An indirect immunofluorescence assay using a cell culture-derived antigen for detection of antibodies to the agent of human granulocytic ehrlichiosis.
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An indirect immunofluorescence assay using a cell culture-derived antigen for detection of antibodies to the agent of human granulocytic ehrlichiosis.

机译:一种间接免疫荧光测定法,使用源自细胞培养物的抗原来检测针对人类粒细胞埃希氏菌病的抗体。

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An indirect immunofluorescence assay for the detection of human antibodies to the agent of human granulocytic ehrlichiosis (HGE) was developed and standardized. Antigen was prepared from a human promyelocytic leukemia cell line (HL-60) infected with a tick-derived isolate of the HGE agent (USG3). Suitable antigen presentation and preservation of cellular morphology were obtained when infected cells were applied and cultured on the slide, excess medium was removed, and cells were fixed with acetone. Use of a buffer containing bovine serum albumin and goat serum reduced background fluorescence, and use of an immunoglobulin G (gamma-specific) conjugate reduced nonspecific binding. The assay readily detected specific antibody from HGE patients and did not detect antibody from healthy individuals. No significant reactivity was noted in sera from patients with high titers of antibodies to other rickettsial species. We were able to identify antibodies reactive to USG3 antigen in samples from areas where HGE is endemic that had tested negative to other rickettsial agents. Animal sera reactive against Ehrlichia equi or Ehrlichia phagocytophila bound to the HGE antigen, indicating that the assay may be useful for veterinary use. Comparability between two different laboratories was assessed by using coded human sera exchanged between laboratories. Results from the two laboratories were similar, indicating that the assay can be easily integrated into use for routine testing for HGE. The assay was then compared to an assay using horse neutrophils infected with ehrlichiae. The two assays gave comparable results, indicating that the cell culture-derived antigen can be used for testing samples that have been previously tested with E. equi as an antigen. The new assay offers several advantages over other immunofluorescence methods that use animal-derived antigen and is suitable for use in testing for human antibodies to the HGE agent.
机译:间接免疫荧光检测法用于检测人类粒细胞性埃希氏菌病(HGE)试剂的抗体已开发并标准化。抗原是从人类的早幼粒细胞白血病细胞系(HL-60)中制备的,该细胞系感染了tick基因衍生的HGE试剂(USG3)。当将感染的细胞应用于载玻片上并进行培养,去除多余的培养基并用丙酮固定细胞时,可以获得合适的抗原呈递和细胞形态的保存。使用含有牛血清白蛋白和山羊血清的缓冲液可减少背景荧光,而使用免疫球蛋白G(γ特异性)结合物则可减少非特异性结合。该测定法很容易检测到来自HGE患者的特异性抗体,而未检测到来自健康个体的抗体。高滴度其他立克次体抗体的患者血清中未发现明显的反应性。我们能够从HGE流行地区的样本中鉴定出对USG3抗原具有反应性的抗体,这些样本对其他立克次氏病试剂呈阴性。对结合到HGE抗原上的马埃里希氏菌或吞噬埃里希氏菌具有反应性的动物血清,表明该测定法可用于兽医用途。通过使用实验室之间交换的编码人血清,评估了两个不同实验室之间的可比性。这两个实验室的结果相似,表明该测定可轻松整合到HGE的常规检测中。然后将该测定与使用感染了大肠杆菌的马嗜中性白细胞的测定进行比较。两种测定给出了可比较的结果,表明细胞培养物衍生的抗原可用于测试先前已用马马链球菌作为抗原测试的样品。与使用动物源抗原的其他免疫荧光方法相比,该新方法具有多个优势,适用于测试针对HGE试剂的人抗体。

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