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Evaluation of recombinant K39 antigen and various promastigote antigens in sero-diagnosis of visceral leishmaniasis in Bangladesh

机译:孟加拉国内脏利什曼病血清学诊断中重组K39抗原和各种前鞭毛体抗原的评估

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摘要

BackgroundDefinitive diagnosis of visceral leishmaniasis (VL) by demonstrating parasites in tissue smears or by culture involves invasive procedures, technical expertise and adequate laboratory facilities. Endemic countries rely mainly on serological tests to diagnose VL. Currently, the immunochromatographic test incorporating the recombinant K39 antigen (rK39 ICT) is the reference test for rapid diagnosis of VL in the Indian subcontinent. The performance of serological tests using rK39 and other promastigote antigens can vary due to differences in antigen expression, the various hosts and environmental factors. To achieve elimination of VL, diagnostic accuracy will be necessary for active case detection especially in those who carry asymptomatic infections. We evaluated the performance of rK39 ICT, enzyme linked immunosorbent assay using mixed Leishmania promastigotes from different Leishmania species (p-ELISA) and indirect fluorescent antibody test (IFAT) utilizing whole promastigotes from the Leishmania donovani complex for sero-diagnosis of VL in Bangladesh.
机译:背景技术通过证明组织涂片中的寄生虫或通过培养进行内脏利什曼病(VL)的明确诊断涉及侵入性程序,技术专长和足够的实验室设施。流行国家主要依靠血清学检查来诊断VL。目前,结合重组K39抗原的免疫色谱测试(rK39 ICT)是印度次大陆VL快速诊断的参考测试。使用rK39和其他前鞭毛体抗原的血清学测试的性能可能会因抗原表达,各种宿主和环境因素的差异而有所不同。为了消除VL,特别是在那些无症状感染的患者中,要进行积极的病例检测,诊断准确性将是必需的。我们使用来自不同利什曼原虫物种的混合利什曼原虫前鞭毛虫(p-ELISA)和间接荧光抗体试验(IFAT),利用来自利什曼原虫donovani复合体的整个前鞭毛虫对孟加拉国VL进行血清学诊断,评估了rK39 ICT,酶联免疫吸附测定的性能。

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