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一种用于检测高水平罗阿罗阿微丝蚴的新型抗原生物标志物。

A novel antigen biomarker for detection of high-level of Loa loa microfilaremia.

机构信息

Infectious Diseases Division, Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, United States of America.

Infectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, United States of America.

出版信息

PLoS Negl Trop Dis. 2024 Sep 3;18(9):e0012461. doi: 10.1371/journal.pntd.0012461. eCollection 2024 Sep.

Abstract

BACKGROUND

Loiasis is a disease caused by the nematode Loa loa. Serious adverse events sometimes occur in people with heavy L. loa microfilaremia after ivermectin treatment. In regions of Central Africa where loiasis is endemic, this significantly impedes global elimination programs for lymphatic filariasis and onchocerciasis that use mass distribution of ivermectin. Improved diagnostic tests to identify individuals at increased risk of serious adverse events could facilitate efforts to eliminate lymphatic filariasis and onchocerciasis in this region.

METHODS AND FINDINGS

We previously identified the L. loa protein Ll-Bhp-1 in loiasis patient sera. Here, we further characterize Ll-Bhp-1 and report development of an antigen capture ELISA to detect this antigen. This assay detected Ll-Bhp-1 in 74 of 116 (63.8%) loiasis patient sera. Ll-Bhp-1 levels were significantly correlated with L. loa microfilarial counts, and the sensitivity of the assay was highest for samples from people with high counts, (94% and 100% in people with ≥20,000 and ≥50,000 microfilaria per milliliter of blood, respectively). The antigen was not detected in 112 sera from people with other filarial infections, or in 34 control sera from the USA.

CONCLUSIONS

This Ll-Bhp-1 antigen assay is specific for loiasis, and highly sensitive for identifying people with high L. loa microfilarial counts who are at increased risk for serious adverse events after ivermectin treatment. L. loa antigen detection has the potential to facilitate loiasis mapping efforts and programs to eliminate lymphatic filariasis and onchocerciasis in Central Africa.

摘要

背景

罗阿丝虫病是由罗阿丝虫引起的疾病。在伊维菌素治疗后,重度罗阿丝虫微丝蚴血症患者有时会出现严重不良事件。在中非流行地区,这极大地阻碍了使用伊维菌素大规模分发来消除淋巴丝虫病和盘尾丝虫病的全球消除计划。改进的诊断测试可以识别出有发生严重不良事件风险的个体,从而有助于在该地区消除淋巴丝虫病和盘尾丝虫病。

方法和发现

我们之前在罗阿丝虫病患者血清中鉴定了罗阿丝虫蛋白 Ll-Bhp-1。在这里,我们进一步对 Ll-Bhp-1 进行了表征,并报告了开发一种抗原捕获 ELISA 来检测这种抗原的方法。该检测方法在 116 例罗阿丝虫病患者血清中的 74 例(63.8%)中检测到 Ll-Bhp-1。Ll-Bhp-1 水平与罗阿丝虫微丝蚴计数显著相关,并且该检测方法对高计数人群的样本具有最高的灵敏度(计数≥20,000 和≥50,000 微丝蚴/毫升血液的人群分别为 94%和 100%)。该抗原未在 112 例来自其他丝虫感染患者的血清中检测到,也未在 34 例来自美国的对照血清中检测到。

结论

这种 Ll-Bhp-1 抗原检测方法对罗阿丝虫病具有特异性,并且高度敏感,可用于识别微丝蚴计数高的人群,这些人群在伊维菌素治疗后发生严重不良事件的风险增加。罗阿丝虫抗原检测有可能促进罗阿丝虫病绘图工作以及在中非消除淋巴丝虫病和盘尾丝虫病的计划。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f143/11398663/b0a648484498/pntd.0012461.g001.jpg

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