Institute of Parasitology, University of Zurich, Zurich, Switzerland.
Infection. 2012 Apr;40(2):139-52. doi: 10.1007/s15010-011-0205-6. Epub 2011 Nov 11.
Human alveolar (AE) and cystic echinococcosis (CE) caused by the metacestode stages of Echinococcus multilocularis and E. granulosus, respectively, lack pathognomonic clinical signs. Diagnosis therefore relies on the results of imaging and serological studies. The primary goal of this study was to evaluate the efficacy of several easy-to-produce crude or partially purified E. granulosus and E. multilocularis metacestode-derived antigens as tools for the serological diagnosis and differential diagnosis of patients suspicious for AE or CE.
The sera of 51 treatment-naïve AE and 32 CE patients, 98 Swiss blood donors and 38 patients who were initially suspicious for echinococcosis but suffering from various other liver diseases (e.g., liver neoplasia, etc.) were analysed.
According to the results of enzyme-linked immunosorbent assays (ELISA), metacestode-derived antigens of E. granulosus had sensitivities varying from 81 to 97% and >99.9% for the diagnosis of CE and AE, respectively. Antigens derived from E. multilocularis metacestodes had sensitivities ranging from 84 to 91% and >99.9% for the diagnosis of CE and AE, respectively. Specificities ranged from 92 to >99.9%. Post-test probabilities for the differential diagnosis of AE from liver neoplasias, CE from cystic liver lesions, and screening for AE in Switzerland were around 95, 86 and 2.2%, respectively. Cross-reactions with antibodies in sera of patients with other parasitic affections (fasciolosis, schistosomosis, amebosis, cysticercosis, and filarioses) did occur at variable frequencies, but could be eliminated through the use of confirmatory testing.
Different metacestode-derived antigens of E. granulosus and E. multilocularis are valuable, widely accessible, and cost-efficient tools for the serological diagnosis of echinococcosis. However, confirmatory testing is necessary, due to the lack of species specificity and the occurrence of cross-reactions to other helminthic diseases.
人肺泡(AE)和囊型包虫病(CE)分别由细粒棘球蚴和多房棘球蚴的中绦期引起,缺乏特征性的临床体征。因此,诊断依赖于影像学和血清学研究的结果。本研究的主要目的是评估几种易于制备的粗提或部分纯化的细粒棘球蚴和多房棘球蚴中绦期衍生抗原作为疑似 AE 或 CE 患者血清学诊断和鉴别诊断的工具的功效。
分析了 51 例未经治疗的 AE 患者和 32 例 CE 患者、98 名瑞士献血者和 38 名最初怀疑患有包虫病但患有其他肝脏疾病(如肝肿瘤等)的患者的血清。
根据酶联免疫吸附试验(ELISA)的结果,细粒棘球蚴和多房棘球蚴中绦期衍生抗原对 CE 和 AE 的诊断灵敏度分别为 81%至 97%和>99.9%。多房棘球蚴中绦期衍生抗原对 CE 和 AE 的诊断灵敏度分别为 84%至 91%和>99.9%。特异性范围为 92%至>99.9%。AE 与肝肿瘤、CE 与囊性肝病变、瑞士 AE 筛查的鉴别诊断后验概率分别约为 95%、86%和 2.2%。与其他寄生虫感染(肝片吸虫病、血吸虫病、阿米巴病、囊虫病和丝虫病)患者血清中的抗体发生交叉反应的频率不同,但通过使用确认性检测可以消除。
不同的细粒棘球蚴和多房棘球蚴中绦期衍生抗原是包虫病血清学诊断的有价值、广泛可及且具有成本效益的工具。然而,由于缺乏种特异性和与其他蠕虫病的交叉反应,需要进行确认性检测。