Freitas Natália Erdens Maron, Campos Denis Augusto Argolo, Ferreira Randrin Queiroz Viana, Jesus Felipe Silva Santos de, Silva Ângelo Antônio Oliveira, Mota Cristiane Oliveira da, Marchini Fabricio Klerynton, Celedon Paola Alejandra Fiorani, Zanchin Nilson Ivo Tonin, Santos Fred Luciano Neves
Advanced Public Health Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation (FIOCRUZ-BA), Salvador, Brazil.
Interdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation (FIOCRUZ-BA), Salvador, Brazil.
Am J Trop Med Hyg. 2024 Oct 29;112(1):89-95. doi: 10.4269/ajtmh.24-0379. Print 2025 Jan 8.
Chagas disease (CD), a neglected tropical disease caused by Trypanosoma cruzi, is a significant public health issue particularly in Latin America, affecting millions worldwide. Diagnosis is a challenge owing to the genetic diversity of T. cruzi and the complexities involved in selecting antigens for the detection of anti-T. cruzi antibodies. This study evaluated four chimeric recombinant antigens (IBMP-8.1, IBMP-8.2, IBMP-8.3, and IBMP-8.4) designed to enhance diagnostic accuracy by addressing assay variability. We compared the diagnostic performance of these chimeric antigens using indirect ELISA as a diagnostic platform, with three commercial serological assays in Brazil, analyzing 100 serum samples from individuals with confirmed CD and 86 from non-infected controls. The results revealed that all assays and antigens demonstrated an area under the receiver operating characteristic curve of 100%, signifying their exceptional ability to distinguish between CD-positive and CD-negative samples. Notably, the chimeric antigens achieved 100% sensitivity, specificity, accuracy, and kappa index, equaling or surpassing the commercial assays. This research highlights the efficacy of IBMP chimeric antigens as reliable diagnostic tools for CD, suggesting their potential integration into commercial diagnostic platforms to enhance the accuracy and reliability of CD detection.
恰加斯病(CD)是由克氏锥虫引起的一种被忽视的热带病,是一个重大的公共卫生问题,尤其在拉丁美洲,全球数百万人受其影响。由于克氏锥虫的基因多样性以及选择用于检测抗克氏锥虫抗体的抗原所涉及的复杂性,诊断成为一项挑战。本研究评估了四种嵌合重组抗原(IBMP - 8.1、IBMP - 8.2、IBMP - 8.3和IBMP - 8.4),旨在通过解决检测变异性来提高诊断准确性。我们以间接ELISA作为诊断平台,将这些嵌合抗原的诊断性能与巴西的三种商业血清学检测方法进行比较,分析了100份来自确诊CD个体的血清样本和86份来自未感染对照的血清样本。结果显示,所有检测方法和抗原的受试者操作特征曲线下面积均为100%,表明它们具有区分CD阳性和CD阴性样本的卓越能力。值得注意的是,嵌合抗原的灵敏度、特异性、准确性和kappa指数均达到100%,与商业检测方法相当或更高。本研究突出了IBMP嵌合抗原作为CD可靠诊断工具的有效性,表明它们有可能整合到商业诊断平台中,以提高CD检测的准确性和可靠性。