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利用新型多重免疫分析法在无症状的确诊疟疾个体中同时定量检测抗原和宿主因子 C-反应蛋白。

Simultaneous Quantification of Antigens and Host Factor C-Reactive Protein in Asymptomatic Individuals with Confirmed Malaria by Use of a Novel Multiplex Immunoassay.

机构信息

Diagnostics, PATH, Seattle, Washington, USA

Quansys Biosciences, Logan, Utah, USA.

出版信息

J Clin Microbiol. 2019 Jan 2;57(1). doi: 10.1128/JCM.00948-18. Print 2019 Jan.

Abstract

Malaria rapid diagnostic tests (RDTs) primarily detect antigen histidine-rich protein 2 (HRP2) and the malaria-conserved antigen lactate dehydrogenase (LDH) for and other malaria species. The performance of RDTs and their utility is dependent on circulating antigen concentration distributions in infected individuals in a population in which malaria is endemic and on the limit of detection of the RDT for the antigens. A multiplexed immunoassay for the quantification of HRP2, LDH, and all-malaria LDH (pan LDH) was developed to accurately measure circulating antigen concentration and antigen distribution in a population with endemic malaria. The assay also measures C-reactive protein (CRP) levels as an indicator of inflammation. Validation was conducted with clinical specimens from 397 asymptomatic donors from Myanmar and Uganda, confirmed by PCR for infection, and from participants in induced blood-stage malaria challenge studies. The assay lower limits of detection for HRP2, pan LDH, LDH, and CRP were 0.2 pg/ml, 9.3 pg/ml, 1.5 pg/ml, and 26.6 ng/ml, respectively. At thresholds for HRP2, pan LDH, and LDH of 2.3 pg/ml, 47.8 pg/ml, and 75.1 pg/ml, respectively, and a specificity ≥98.5%, the sensitivities for ultrasensitive PCR-confirmed infections were 93.4%, 84.9%, and 48.9%, respectively. LDH (pLDH) concentration, in contrast to that of HRP2, correlated closely with parasite density. CRP levels were moderately higher in infections with confirmed antigenemia versus those in clinical specimens with no antigen. The 4-plex array is a sensitive tool for quantifying diagnostic antigens in malaria infections and supporting the evaluation of new ultrasensitive RDTs.

摘要

疟疾快速诊断检测(RDT)主要检测抗原组氨酸丰富蛋白 2(HRP2)和乳酸脱氢酶(LDH),用于和其他疟原虫。RDT 的性能和其应用取决于疟疾流行地区感染个体中循环抗原浓度分布以及 RDT 对这些抗原的检测限。开发了一种用于定量检测 HRP2、LDH 和全疟原虫 LDH(pan LDH)的多重免疫测定法,以准确测量流行地区疟疾人群中的循环抗原浓度和抗原分布。该测定法还测量 C-反应蛋白(CRP)水平作为炎症的指标。该测定法在缅甸和乌干达的 397 名无症状供体的临床标本中进行了验证,这些标本通过 PCR 检测感染,以及在诱导的血期疟疾挑战研究中参与者的标本。该测定法对 HRP2、pan LDH、LDH 和 CRP 的检测下限分别为 0.2pg/ml、9.3pg/ml、1.5pg/ml 和 26.6ng/ml。在 HRP2、pan LDH 和 LDH 的阈值分别为 2.3pg/ml、47.8pg/ml 和 75.1pg/ml 时,特异性≥98.5%,超敏 PCR 确诊感染的敏感性分别为 93.4%、84.9%和 48.9%。与 HRP2 相比,LDH(pLDH)浓度与寄生虫密度密切相关。与无抗原的临床标本相比,抗原血症确诊感染的 CRP 水平中度升高。4 plex 阵列是一种敏感的工具,可用于定量检测疟疾感染中的诊断抗原,并支持新的超敏 RDT 的评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98f2/6322473/5874ad62502e/JCM.00948-18-f0001.jpg

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