Effectiveness ofFasciola giganticaexcretory-secretory and recombinant cathepsin L antigens for rapid diagnosis of human fascioliasis using immunochromatographic devices

被引:5
|
作者
Sadaow, Lakkhana [1 ,2 ,3 ,4 ]
Yamasaki, Hiroshi [5 ]
Morishima, Yasuyuki [5 ]
Sanpool, Oranuch [1 ,2 ,3 ,4 ]
Rodpai, Rutchanee [1 ,2 ,3 ,4 ]
Janwan, Penchom [6 ]
Boonroumkaew, Patcharaporn [1 ,2 ,3 ,4 ]
Maleewong, Wanchai [1 ,2 ,3 ,4 ]
Intapan, Pewpan M. [1 ,2 ,3 ,4 ]
机构
[1] Khon Kaen Univ, Fac Med, Dept Parasitol & Excellence Med Innovat, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Fac Med, Technol Res Grp, Khon Kaen 40002, Thailand
[3] Khon Kaen Univ, Fac Med, Dept Parasitol, Khon Kaen 40002, Thailand
[4] Khon Kaen Univ, Mekong Hlth Sci Res Inst, Khon Kaen 40002, Thailand
[5] Natl Inst Infect Dis, Dept Parasitol, Minist Hlth Labour & Welf, Tokyo 1628640, Japan
[6] Walailak Univ, Sch Allied Hlth Sci, Dept Med Technol, Nakhon Si Thammarat 80161, Thailand
关键词
Human fascioliasis; Serodiagnosis; Antibody detection; Immunochromatographic test; Point-of-care test; LINKED-IMMUNOSORBENT-ASSAY; HEPATICA; IMMUNODIAGNOSIS; SERODIAGNOSIS; ANTIBODIES; EPIDEMIOLOGY;
D O I
10.1007/s00436-020-06907-w
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Fascioliasis, a food- and water-borne trematodiasis, has been identified as a public health threat by the World Health Organization, with millions of people estimated to be infected or at risk of infection worldwide. We developed an immunochromatographic test (ICT) as a point-of-care (POC) tool for the rapid serodiagnosis of human fascioliasis caused byFasciola giganticaand evaluated their diagnostic ability. Two tests were developed using antigens from adultF. giganticaexcretory-secretory (ES) product and recombinantF. giganticacathepsin L (rFgCL). Sera from 12 patients with parasitologically proven fascioliasis caused byF. gigantica, 18 with clinically suspected fascioliasis, 65 with other parasitic infections, and 30 healthy controls were used. Using a cutoff of > 0.5 for antibody detection, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of the ES-based ICT method were 100%, 98.9% 96.8%, 100%, and 99.2%, respectively, and those of the rFgCL-based ICT method were 86.7%, 93.7%, 81.3%, 95.7%, and 92.0%, respectively. The concordance between the two methods was 91.2%. Tests usingF. giganticaES and rFgCL antigens can be employed quickly and easily as POC diagnostic tools. They can be used to support the clinical diagnosis of human fascioliasis gigantica and in large-scale surveys in endemic areas throughout tropical regions without necessitating additional facilities or ancillary supplies.
引用
收藏
页码:3691 / 3698
页数:8
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