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巴西利什曼原虫和秘鲁利什曼原虫抗原在免疫印迹法中检测美洲皮肤利什曼病的诊断性能。

Diagnostic performance of Leishmania braziliensis and Leishmania peruviana antigens in the immunoblot method for the detection of american tegumentary leishmaniasis.

机构信息

Centro Nacional de Salud Pública, Instituto Nacional de Salud, Lima, Perú.

Centro Nacional de Alimentación, Nutrición y Vida Saludable, Instituto Nacional de Salud, Lima, Perú.

出版信息

Rev Peru Med Exp Salud Publica. 2024 Oct 21;41(3):294-300. doi: 10.17843/rpmesp.2024.413.13231.

Abstract

BACKGROUND

Motivation for the study. To contribute to the immunogenic character of soluble and excretion/secretion antigens of Leishmania braziliensis and Leishmania peruviana with the aim of identifying proteins with diagnostic potential.

BACKGROUND

Main findings. The soluble antigen of Leishmania braziliensis has a sensitivity in the detection of ATL of 87.7%, specificity of 100% and a false positive rate of 20% against sera from patients with Chagas disease and 8.3% with mycosis.

BACKGROUND

Implications. Immunoblot can improve the resolution capacity in the serological diagnosis of American tegumentary Leishmaniasis, particularly in patients where the length of the disease and the clinical form make difficult the diagnosis by parasitological methods.

BACKGROUND

This study aimed to determine the performance of Leishmania braziliensis and Leishmania peruviana antigens in the detection of ATL by using serum samples obtained between 2013 - 2016. The obtained soluble and excretion/secretion antigens were transferred to membrane nitrocellulose by immunoblot assay. The evaluation was carried out against sera confirmed for ATL, at a confidence level of 95%, determining that the soluble antigen of Leishmania braziliensis had a sensitivity of 87.7%, specificity of 100% and area under the curve of 0.95; on the other hand, Leishmania peruviana showed values of 92.3%, 95.7% and 0.94, respectively. According to the results, we recommend that the reported immunogenic regions should be characterized and analyzed in order to continue with the development of recombinant and synthetic proteins, aimed at improving the efficiency of the serological diagnosis of the disease.

摘要

背景

研究动机。为了研究巴西利什曼原虫和秘鲁利什曼原虫可溶性和分泌/排泄抗原的免疫原性特征,旨在鉴定具有诊断潜力的蛋白质。

背景

主要发现。巴西利什曼原虫可溶性抗原对 ATL 的检测灵敏度为 87.7%,特异性为 100%,假阳性率为 20%(针对恰加斯病患者的血清),8.3%(针对真菌感染患者的血清)。

背景

意义。免疫印迹可以提高对美洲皮肤利什曼病血清学诊断的分辨率能力,特别是在疾病持续时间长且临床形式使寄生虫学方法的诊断变得困难的患者中。

背景

本研究旨在使用 2013-2016 年获得的血清样本,确定巴西利什曼原虫和秘鲁利什曼原虫抗原在 ATL 检测中的性能。获得的可溶性和分泌/排泄抗原通过免疫印迹转移到硝酸纤维素膜上。在 95%置信水平下,对经确认的 ATL 血清进行评估,结果表明巴西利什曼原虫可溶性抗原的灵敏度为 87.7%,特异性为 100%,曲线下面积为 0.95;另一方面,秘鲁利什曼原虫的灵敏度分别为 92.3%、95.7%和 0.94。根据结果,我们建议对报道的免疫原性区域进行特征分析,以便继续开发重组和合成蛋白,从而提高疾病的血清学诊断效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a6a/11495926/2cdef0a3a2d0/rpmesp-41-03-13231-g001.jpg

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