Ossowski Micaela S, Silva Ângelo Antônio Oliveira, Santos Emily Ferreira, Leony Leonardo Maia, Santos Fred Luciano Neves, Gómez Karina A
Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres" (INGEBI-CONICET), Buenos Aires, Argentina.
Advanced Health Public Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation (FIOCRUZ-BA), Salvador, Brazil.
Front Microbiol. 2025 Jun 10;16:1605755. doi: 10.3389/fmicb.2025.1605755. eCollection 2025.
The diagnosis of chronic infection with the parasite relies on detecting specific IgG antibodies using two or three (in the case of discordance) serological assays based on different principles. This diagnostic algorithm poses challenges in identifying patients with chronic Chagas disease (CCD), particularly in endemic areas where financial and human resources are scarce. The discovery of new antigens capable of achieving 100% sensitivity and specificity is a priority in this field. Previously, we introduced two recombinant domains, designated as rTcD3 and rTcD6 derived from a hypothetical protein from , as potential candidates for the diagnosis of CCD. In the current study, we extended our results by assessing the diagnostic accuracy of rTcD3 and rTcD6 in a large cohort of infected and non-infected individuals from various regions of Brazil. Both antigens showed a specificity of 97.9%, while sensitivity was 79.5% for rTcD3 and 81.5% for rTcD6. In addition, cross-reactivity analysis on 764 samples from individuals with other parasitic, bacterial and viral infections was estimated to be less than 0.9%. Specifically, one (for rTcD3) and two (for rTcD6) samples positive for leptospirosis reacted with both antigens, while 2 out of 764 samples from individuals infected with spp., resulted in a false positive for rTcD3, while four samples behaved similarly for rTcD6. Furthermore, a false-positive reaction was also observed in one HIV-positive sample rTcD6. In conclusion, this study provides further evidence supporting the diagnostic potential of a specific and sensitive IgG-ELISA based on rTcD3 and rTcD6 for detecting chronic infection across various regions of the Americas, with minimal cross-reactivity with other pathogens.
对该寄生虫慢性感染的诊断依赖于使用基于不同原理的两种或三种(在结果不一致的情况下)血清学检测方法来检测特异性IgG抗体。这种诊断算法在识别慢性恰加斯病(CCD)患者方面存在挑战,尤其是在财政和人力资源匮乏的流行地区。发现能够实现100%敏感性和特异性的新抗原是该领域的一个优先事项。此前,我们引入了两个重组结构域,分别命名为rTcD3和rTcD6,它们源自一种假设蛋白,作为CCD诊断的潜在候选物。在当前研究中,我们通过评估rTcD3和rTcD6在来自巴西不同地区的大量感染和未感染个体队列中的诊断准确性,扩展了我们的研究结果。两种抗原的特异性均为97.9%,而rTcD3的敏感性为79.5%,rTcD6的敏感性为81.5%。此外,对来自患有其他寄生虫、细菌和病毒感染个体的764份样本进行的交叉反应性分析估计低于0.9%。具体而言,一份钩端螺旋体病阳性样本(针对rTcD3)和两份(针对rTcD6)与两种抗原均发生反应,而来自感染 spp.个体的764份样本中有两份导致rTcD3出现假阳性,针对rTcD6有四份样本表现类似。此外,在一份HIV阳性样本中rTcD6也观察到假阳性反应。总之,本研究提供了进一步的证据,支持基于rTcD3和rTcD6的特异性和敏感IgG-ELISA在检测美洲不同地区慢性 感染方面的诊断潜力,与其他病原体的交叉反应性最小。