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首页> 外文期刊>Pathogens and global health >Diagnostic potential of monoclonal antibodies developed against C-terminal polypeptide of P. falciparum Histidine Rich Protein2 (PfHRP2) in malaria infected patients from India
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Diagnostic potential of monoclonal antibodies developed against C-terminal polypeptide of P. falciparum Histidine Rich Protein2 (PfHRP2) in malaria infected patients from India

机译:对印度疟疾感染患者的疟原虫组蛋白2(PFHRP2)富含C末端多肽的单克隆抗体的诊断潜力

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Malaria, caused by Plasmodium falciparum has become a major health burden in most tropical and developing countries. P. falciparum Histidine Rich Protein2 (PfHRP2), which exhibits polymorphism, is being widely used as a diagnostic marker. Recently, we reported the development of monoclonal antibodies against conserved C-terminal 105 amino acids of PfHRP2 for malaria diagnosis. Now, in this study, the diagnostic performance of two anti-C-terminal PfHRP2 mAbs (b10c1 and Aa3c10) were evaluated with 100 blood samples from clinically identified malaria patients from seven different geographical centers in India. Sandwich ELISA, polymerase chain reaction (PCR) and statistical tools were used for the evaluation of the performance of the anti-C-terminal PfHRP2 mAb. These mAbs detected P. falciparum (mean OD value 1.525 +/- 0.56) malaria with great accuracy with no cross reactivity with P. Plasmodium vivax (mean OD value 0.285 +/- 0.051) and normal healthy control samples (mean OD value 0.185 +/- 0.06) in Sandwich ELISA assay. The samples which were RDT negative for P. falciparum were also reactive in Sandwich ELISA with mean OD value of (1.303 +/- 0.532). The amount of PfHRP2 antigen in the patients' blood sample was quantified and categorized into three distinct groups having the HRP2 antigen in high, intermediate and low amounts. The presence of Pfhrp2 gene was also confirmed by PCR analysis. The sensitivity and specificity of the mAb were found to be 95 and 96% respectively. These data strongly suggest that the anti-C-terminal PfHRP2 mAbs b10c1 and Aa3c10 have merits for improvising the existing malarial diagnostics.
机译:疟疾,由疟原虫引起的恶性疟原虫引起的是大多数热带和发展中国家的重大健康负担。 P. falciparum组氨酸富含蛋白质2(pfhrp2),其具有多态性,被广泛用作诊断标志物。最近,我们报道了对疟疾诊断的PFHRP2的保守C末端105氨基酸的单克隆抗体的发展。现在,在本研究中,使用来自印度的七个不同地理中心的临床鉴定的疟疾患者的100个血液样本评估了两种抗C末端PFHRP2 mAb(B10C1和AA3C10)的诊断性能。夹心ELISA,聚合酶链反应(PCR)和统计工具用于评估抗C末端PFHRP2 mAb的性能。这些mAbs检测到p. falciparum(平均值1.525 +/- 0.56)疟疾,具有极高的准确性,没有交叉反应性与p.疟原虫vivax(平均异常值0.285 +/- 0.051)和正常的健康对照样品(平均值0.185 + / - 0.06)在夹层ELISA测定中。对于P. falciparum的RDT阴性的样品在夹心ELISA中也是反应性的,其平均OD值(1.303 +/- 0.532)。量化患者血液样品中的PFHRP2抗原的量,并将其分为三个不同的基团,其具有高,中间体和低量的HRP2抗原。通过PCR分析还证实了PFHRP2基因的存在。发现MAB的敏感性和特异性分别为95和96%。这些数据强烈表明,抗C末端PFHRP2 mAb B10C1和AA3C10具有改善现有疟疾诊断的优点。

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