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首页> 外文期刊>Journal of Clinical Microbiology >Two-site immunoradiometric assay for detection of Plasmodium falciparum antigen in blood using monoclonal and polyclonal antibodies.
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Two-site immunoradiometric assay for detection of Plasmodium falciparum antigen in blood using monoclonal and polyclonal antibodies.

机译:使用单克隆和多克隆抗体的两点免疫放射测定法检测血液中的恶性疟原虫抗原。

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Three systems of immunoradiometric assays (IRMAs), a two-site monoclonal antibody sandwich IRMA (MAb-IRMA), two-site polyclonal antibody-monoclonal antibody sandwich IRMA (PAb-MAb-IRMA), and two-site polyclonal antibody sandwich IRMA (PAb-IRMA), were developed to detect low-grade infections with Plasmodium falciparum. The assays showed good correlation with parasitemia when tested against parasites from in vitro cultures (r = 0.996, 0.994, and 0.998 for MAb-, PAb-MAb-, and PAb-IRMA, respectively), with the ability to detect as few as 0.24, 0.67, and 1.82 parasites per 10(7) erythrocytes, respectively. The assays were specific for P. falciparum, since a serially diluted specimen from a patient with vivax malaria with an initial parasitemia of 0.8% and almost all of the undiluted specimens from five other vivax malaria patients were negative. The assays were performed on patients with falciparum malaria before and after treatment with antimalarial drugs. Before treatment, all 24 patients were positive by all three systems of two-site sandwich IRMAs. Two weeks after treatment, 81.8% (18 of 22) of the patients were positive by microscopic examination, but the IRMA positivity rates were 90.9% (20 of 22), 86.4% (19 of 22), and 81.8% (18 of 22) for MAb-, PAb-MAb-, and PAb-IRMA, respectively. Four weeks after treatment, all 19 patients were negative by microscopic examination, but 52.6% (10 of 19) of the patients were still positive with MAb- and PAb-MAb-IRMA and 31.6% (6 of 19) were positive with PAb-IRMA. Comparison between the three systems of IRMA showed that the MAb-IRMA was superior to the other two systems for three reasons. First, it gave a lower count when tested with blood from healthy individuals. Second, it gave a higher count when tested with blood from patients with falciparum malaria. Third, it gave better correlation with parasitemia when blood from falciparum malaria patients was tested. MAb-IRMA is recommended for use for the detection of low-grade P. falciparum infection.
机译:三种免疫放射测定(IRMA)系统,两点单克隆抗体三明治IRMA(MAb-IRMA),两点多克隆抗体-单克隆抗体三明治IRMA(PAb-MAb-IRMA)和两点多克隆抗体三明治IRMA( PAb-IRMA)被开发用于检测恶性疟原虫的低度感染。当针对体外培养物中的寄生虫进行测试时,该检测方法与寄生虫病显示出良好的相关性(MAb-,PAb-MAb-和PAb-IRMA分别为r = 0.996、0.994和0.998),检出能力仅为0.24每10(7)个红细胞中分别有0.67和1.82个寄生虫。该测定法对恶性疟原虫具有特异性,因为来自间日疟原虫患者的系列稀释标本的初始寄生虫病率为0.8%,而来自其他五名间日疟原虫患者的几乎所有未稀释标本均为阴性。在使用抗疟药治疗之前和之后,对恶性疟疾患者进行了测定。在治疗前,所有24例患者的两部位三明治IRMA的所有三个系统均为阳性。治疗后两周,镜检阳性率为81.8%(22名中的18名),但IRMA阳性率为90.9%(22名中的20名),86.4%(22名中的19名)和81.8%(22名中的18名) )分别用于MAb-,PAb-MAb-和PAb-IRMA。治疗后四周,所有19例患者的镜检结果均为阴性,但52.6%(19中的10)患者仍然是MAb-和PAb-MAb-IRMA阳性的,而31.6%(19中的6)患者的PAb-仍然是阳性的IRMA。三个IRMA系统之间的比较表明,MAb-IRMA优于其他两个系统的原因有三个。首先,当用健康人的血液测试时,它的计数较低。其次,当用恶性疟疾患者的血液进行检测时,其计数更高。第三,当测试恶性疟疾患者的血液时,它与寄生虫病具有更好的相关性。建议将MAb-IRMA用于检测低度恶性疟原虫感染。

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