Kochanowski Maciej, González-Muñoz Miguel, Gómez-Morales María Ángeles, Gottstein Bruno, Dąbrowska Joanna, Różycki Mirosław, Cencek Tomasz, Müller Norbert, Boubaker Ghalia
Department of Parasitology and Invasive Diseases, National Veterinary Research Institute, Partyzantów Avenue 57, 24-100, Puławy, Poland.
University Hospital La Paz-FIBHULP, Paseo Castellana, 261, 28046, Madrid, Spain.
Exp Parasitol. 2019 Feb;197:9-15. doi: 10.1016/j.exppara.2018.12.004. Epub 2018 Dec 22.
Serodiagnosis of human anisakidosis is presently hampered by the current lack of standardised serological assays that allow sensitive and specific detection of Anisakidae-specific antibodies in human patients. In the present study, we comparatively evaluated the diagnostic value (by IgG-ELISA) of excretory-secretory antigens (ESAgs) of Anisakis simplex, Pseudoterranova decipiens and Contracaecum osculatum, representing the most frequently found genera responsible for human infection. In addition, we tested also a mix of the three ES preparations (Mix-ESAgs) as well as two recombinant allergens of A. simplex, rAni s 1 and rAni s 7. ES antigen from C. osculatum yielded the best diagnostic performance in IgG-ELISA-based serodiagnosis of the Spanish anisakidosis patients investigated in this study (relative serodiagnostic sensitivity 100%; specificity 89%) as compared to A. simplex ES-antigen (93% versus 57%) and P. decipiens (67% versus 93%) or a mix of the three ES antigens (100% versus 44%), respectively. Cross-reactions of C. osculatum ES antigen with serum-antibodies from patients suffering from other helminth infections were rare and were exclusively found with few sera from toxocariasis, ascariasis, and filariasis patients. The two recombinant allergens rAni s 1 and rAni s 7 did not prove sufficiently sensitive and specific in order to justify a further evaluation of these antigens regarding their suitability in IgG-ELISA-based serodiagnosis of human anisakidosis. In conclusion, the C. osculatum-ESAg-ELISA remains as key candidate to be further assessed for the serodiagnosis of symptomatic anisakidosis in different endemic regions.
目前,人类异尖线虫病的血清学诊断受到阻碍,因为目前缺乏标准化的血清学检测方法,无法灵敏且特异地检测出人类患者体内异尖线虫科特异性抗体。在本研究中,我们比较评估了简单异尖线虫、欺骗新蛔线虫和吻状对盲囊线虫排泄分泌抗原(ESAgs)的诊断价值(通过IgG-ELISA法),这三种线虫代表了导致人类感染的最常见属。此外,我们还测试了三种ES制剂的混合物(混合ESAgs)以及简单异尖线虫的两种重组变应原rAni s 1和rAni s 7。在本研究中对西班牙异尖线虫病患者进行的基于IgG-ELISA的血清学诊断中,吻状对盲囊线虫的ES抗原表现出最佳诊断性能(相对血清学诊断敏感性为100%;特异性为89%),相比之下,简单异尖线虫ES抗原的相应数据分别为93%和57%,欺骗新蛔线虫的相应数据分别为67%和93%,三种ES抗原混合物的相应数据分别为100%和44%。吻状对盲囊线虫ES抗原与其他蠕虫感染患者血清抗体的交叉反应很少,仅在少数弓蛔虫病、蛔虫病和丝虫病患者的血清中发现。两种重组变应原rAni s 1和rAni s 7在敏感性和特异性方面表现不足,因此无法进一步评估它们在基于IgG-ELISA的人类异尖线虫病血清学诊断中的适用性。总之,吻状对盲囊线虫ESAg-ELISA仍是不同流行地区有症状异尖线虫病血清学诊断的关键候选方法,有待进一步评估。