环孢子子抗体检测在无免疫旅行者中作为检测恶性疟原虫感染血清流行病学工具的评价。

T Jelinek, H D Nothdurft, T Löscher
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引用次数: 0

摘要

这项调查的目的是收集有关无免疫人群接触一次疟疾感染后的cs抗体水平和免疫反应持续时间的数据。为此目的,使用市售的ELISA检测试剂盒调查了来自98名确诊恶性疟疾患者的156份标本、来自64名间日疟疾患者的76份标本和来自32名以前未到过疟疾地区的患者的血清。还通过间接荧光抗体试验(IFAT)对来自恶性疟疾患者的所有标本进行了merozoite抗体检测。在症状出现后的第8天至第90天期间,该小组中89.1%的标本中检测到merozote抗体阳性水平,此后稳步下降。在出现症状后的头7天内,36.4%的恶性疟疾患者标本的cs抗体检测结果呈阳性。在发病后第8-90天,这一数字上升到55.8%,在之后(91-1898天)的标本中,这一数字下降到38.9%。11份标本cs抗体检测呈阳性,但IFAT阴性。因此,在第0天和第7天,IFAT或CS-ELISA检测的标本百分比为51.9% (p < 0.001),在第8天和第90天检测的标本百分比为95.3% (p = 0.039),之后检测的标本百分比为44.4% (p < 0.001)。在5.3%的间日疟疾患者标本中也可检测到cs抗体,而疟疾阴性对照组的血清均未检测到cs抗体阳性。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of circumsporozoite antibody testing as a sero-epidemiological tool for the detection of Plasmodium falciparum infection in non-immune travelers.

The objective of this investigation was to collect data concerning CS-antibody levels and duration of the immunological response to exposure of non-immune persons to a single malaria infection. For this purpose 156 specimens from 98 patients with confirmed falciparum malaria, 76 specimen derived from 64 patients with vivax malaria and sera from 32 patients who had not been previously to malarious areas were investigated by use of a commercially available ELISA testkit. All specimens from patients with falciparum malaria were also tested for merozoite-antibodies by an indirect fluorescence antibody test (IFAT). Positive levels of merozoite-antibodies were detectable in 89.1% of the specimen in this panel during the period between days 8 and 90 after onset of symptoms and decreased steadily thereafter. The test results were positive for CS-antibodies in 36.4% of the specimens from patients with falciparum malaria during the first 7 days after onset of symptoms. This figure increased to 55.8% during days 8-90 after onset and decreased to 38.9% in specimens which were tested later (91-1898 days). 11 specimens reacted positively to CS-antibody testing but negative in the IFAT. Therefore, the percentage of specimen detected by either IFAT or CS-ELISA was at 51.9% during days 0 and 7 (p < 0.001), 95.3% during days 8 and 90 (p = 0.039) and 44.4% for testing performed later (p < 0.001). CS-antibodies could also be detected in 5.3% of specimen from patients with vivax malaria while none of the sera from the malaria-negative control-group tested positive for CS-antibodies.(ABSTRACT TRUNCATED AT 250 WORDS)

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