Bosqui Larissa R, Gonçalves Ana Lúcia R, Gonçalves-Pires Maria do Rosário F, Custodio Luiz Antonio, de Menezes Maria Cláudia N D, Murad Valter A, de Paula Fabiana M, Pavanelli Wander R, Conchon-Costa Ivete, Costa-Cruz Julia Maria, Costa Idessania N
Departamento de Ciências Patológicas, Laboratório de Parasitologia, Universidade Estadual de Londrina, PR, Brazil.
Departamento de Imunologia, Microbiologia e Parasitologia, Instituto de Ciências Biomédicas, Universidade Federal de Uberlândia, MG, Brazil.
Acta Trop. 2015 Oct;150:190-5. doi: 10.1016/j.actatropica.2015.07.026. Epub 2015 Jul 31.
Human strongyloidiasis is an infection caused by the helminth Strongyloides stercoralis that can be fatal, especially in immunosuppressed patients. The aim of this study is to evaluate parasite-specific IgG and IgA levels using S. venezuelensis third-stage (L3) infective larvae alkaline extract as a heterologous antigen by ELISA in paired serum and saliva samples with improved sensitivity and specificity. Individuals from northern Paraná state, Brazil were divided into three groups: 30 patients copropositive for S. stercoralis (Group I); 30 clinically healthy individuals (Group II); and 30 patients copropositive for other parasites (Group III). The area under ROC curve (AUC), an overall index of diagnostic accuracy, and Kappa index were calculated. Data were analyzed using analysis of variance (ANOVA) followed by a Kruskal-Wallis test. Probability (p) values of <0.05 were regarded as significant. In Group I, IgG was detected in 96.7% serum and in 6.7% saliva samples. IgG was not detected in Group II. In Group III, cross-reactivity was observed for serum IgG in 26.7% and in 6.7% for saliva samples. In Group I, IgA was detected in 76.7% serum and 56.7% saliva samples. In Group II, 3.3% were positive for IgA in serum, whereas IgA was not detected in any saliva samples. Group III showed 6.7% serum and 26.7% saliva-positive samples. The sensitivity values for detection of IgG and IgA in serum samples were 96.7% and 76.7%, respectively. In saliva samples, the sensitivity values for detection of IgG and IgA were 6.7% and 56.7%, respectively. The specificity value was 100% for the detection of IgG in serum and for detection of IgG and IgA in saliva, and 96.7% for detection of IgA in serum samples. The proper choice of immunological diagnosis to supplement parasitological methods is essential to estimate the true prevalence of the parasite, and will permit analysis of population immune response profiles, particularly in northern Paraná state, where there are no previous reports.
人体类圆线虫病是由蠕虫粪类圆线虫引起的一种感染,可能会致命,尤其是在免疫抑制患者中。本研究的目的是通过酶联免疫吸附测定法(ELISA),使用委内瑞拉类圆线虫第三期(L3)感染性幼虫碱性提取物作为异源抗原,在配对的血清和唾液样本中评估寄生虫特异性IgG和IgA水平,以提高敏感性和特异性。来自巴西巴拉那州北部的个体被分为三组:30名粪类圆线虫粪检阳性患者(第一组);30名临床健康个体(第二组);以及30名其他寄生虫粪检阳性患者(第三组)。计算了诊断准确性的总体指标即ROC曲线下面积(AUC)和Kappa指数。数据采用方差分析(ANOVA),随后进行Kruskal-Wallis检验。概率(p)值<0.05被视为具有显著性。在第一组中,96.7%的血清样本和6.7%的唾液样本中检测到IgG。第二组中未检测到IgG。在第三组中,26.7%的血清样本和6.7%的唾液样本中观察到血清IgG交叉反应。在第一组中,76.7%的血清样本和56.7%的唾液样本中检测到IgA。在第二组中,3.3%的血清IgA呈阳性,而任何唾液样本中均未检测到IgA。第三组显示6.7%的血清样本和26.7%的唾液样本呈阳性。血清样本中检测IgG和IgA的敏感性值分别为96.7%和76.7%。在唾液样本中,检测IgG和IgA的敏感性值分别为6.7%和56.7%。血清中IgG检测的特异性值为100%,唾液中IgG和IgA检测的特异性值为100%,血清样本中IgA检测的特异性值为96.7%。正确选择免疫诊断方法以补充寄生虫学方法对于估计寄生虫的真实流行率至关重要,并且将有助于分析人群免疫反应谱,特别是在巴拉那州北部,此前尚无相关报道。