Parasitology Laboratory Wadsworth Center, New York State Department of Health, Albany, NY 12208.
Division of Infectious Diseases, New York Medical College, Valhalla, NY 10595.
Diagn Microbiol Infect Dis. 2020 May;97(1):115008. doi: 10.1016/j.diagmicrobio.2020.115008. Epub 2020 Jan 29.
Multiple methodologies have been used to detect antibodies to Babesia microti. Use of an indirect immunofluorescence assay (IFA) has been the most widely used approach, but IFAs have varied as to which antibody class or classes are being detected and in regard to cutoff titers. In this study, 245 different patients with polymerase chain reaction (PCR)-confirmed B. microti infection were tested by a polyvalent IFA using serum collected within 3 days of the date the blood sample for PCR testing was obtained. Of the 245 patients, 243 (99.2%) had a positive serologic test result (i.e., ≥1:64). Of the 243 patients who were seropositive, 242 (99.6%) had a titer of ≥1:256, 236 (97.1%) had a titer of ≥1:512, and 210 (86.4%) had a titer of ≥1:1024. In conclusion, high titer seropositivity based on a polyvalent IFA is to be expected at the time of PCR confirmation of active babesiosis in clinical practice.
已经使用了多种方法来检测微小巴贝斯虫抗体。间接免疫荧光分析(IFA)的应用最为广泛,但 IFA 在检测哪种抗体类别或类别以及截止滴度方面存在差异。在这项研究中,使用多价 IFA 检测了 245 名经聚合酶链反应(PCR)确认的微小巴贝斯虫感染的不同患者,这些患者的血清采集时间在用于 PCR 检测的血液样本采集日期后的 3 天内。在 245 名患者中,243 名(99.2%)血清学检测结果呈阳性(即≥1:64)。在 243 名血清阳性患者中,242 名(99.6%)的滴度≥1:256,236 名(97.1%)的滴度≥1:512,210 名(86.4%)的滴度≥1:1024。总之,在临床实践中,PCR 确认活性巴贝斯虫感染时,预计会出现基于多价 IFA 的高滴度血清阳性。