Comparison of the serological tests ICT and ELISA for the diagnosis of alveolar echinococcosis in France

被引:19
作者
Knapp, Jenny [1 ,2 ]
Sako, Yasuhito [3 ]
Grenouillet, Frederic [1 ,2 ,4 ]
Bresson-Hadni, Solange [2 ,5 ]
Richou, Carine [2 ,5 ]
Gbaguidi-Haore, Houssein [1 ,6 ]
Ito, Akira [3 ]
Millon, Laurence [1 ,2 ,4 ]
机构
[1] Fac Med & Pharm, Lab Chrono Environm, UMR CNRS 6249, Besancon, France
[2] WHO Collaborating, Ctr Prevent & Treatment Human Echinococcosis, Besancon, France
[3] Asahikawa Med Univ, Dept Parasitol, Asahikawa, Hokkaido, Japan
[4] Univ Hosp Besancon, Lab Parasitol Mycol, Besancon, France
[5] Univ Hosp Besancon, Dept Hepatol, Besancon, France
[6] Univ Hosp Besancon, Lab Hosp Hyg, Besancon, France
关键词
alveolar echinococcosis; diagnosis; rEm18; immunochromatography; rapid test; rEm18-ELISA and Em2-Em18-ELISA tests; RECOMBINANT EM18; FOLLOW-UP; ANTIGEN; DIFFERENTIATION; IMMUNODIAGNOSIS; INFECTIONS;
D O I
10.1051/parasite/2014037
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
Serological diagnosis of alveolar echinococcosis (AE) is a key element for efficient patient treatment management. A rapid immunochromatography test kit (ICT) using the recombinant Em18 antigen (rEm18) was recently developed. The aim of our study was to assess this test on a panel of sera from French patients with alveolar echinococcosis and control patients. In a blind test, a total of 112 serum samples were tested including samples of AE (n = 30), cystic echinococcosis [CE] (n = 15), and polycystic echinococcosis [PE] (n = 1). For the comparison, 66 sera from patients with hepatocarcinoma, fascioliasis, toxocariasis, Caroli's disease, or autoimmune chronic active hepatitis were used. The diagnostic test sets we used were the rEm18-ICT and two validated ELISAs with rEm18 and Em2-Em18 antigens, respectively. For the ICT, 27/30 sera from AE patients, 4/15 sera from CE patients and the PE patient serum were positive. One serum from the control panel (toxocariasis) was positive for the ICT. The rEm18-ICT sensitivity (90.0%) and specificity (92.7%) for detection of Em18-specific antibodies confirmed it as a relevant tool for AE diagnosis. The rEm18-ELISA had a sensitivity of 86.7% and specificity of 91.5%, and the Em2-Em18-ELISA had a sensitivity of 96.7% and specificity of 87.8%. However, when AE patient sera are recorded as weak in intensity with the ICT, we recommend a double reading and use of a reference sample if the ICT is used for patient follow-up.
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