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首页> 外文期刊>Annals of tropical medicine and parasitology >Detection of filaria-specific IgG4 antibodies and filarial DNA, for the screening of blood spots for Brugia timori.
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Detection of filaria-specific IgG4 antibodies and filarial DNA, for the screening of blood spots for Brugia timori.

机译:检测丝状菌特异性IgG4抗体和丝状DNA,以筛查布鲁格氏菌血斑。

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The establishment of simple, sensitive and specific tools for the diagnosis of brugian lymphatic filariasis is a prerequisite for a successful intervention to control the disease. In the simple and rapid Brugia Rapid (BR) test, an immunochromatographic dipstick is used to detect IgG(4) antibodies that are reactive with a recombinant Brugia malayi antigen. When sera from 109 individuals with Brugia microfilaraemias (12 with B. malayi and 97 with B. timori) were investigated using the BR test, all were found positive. In contrast, all of the 150 sera from individuals with Onchocerca volvulus or Mansonella infections investigated were found negative in BR tests. Some unwelcome cross-reactions were observed, however, with sera from individuals infected with Wuchereria bancrofti (three of 12 test-positive) and Dirofilaria (one of nine test-positive). In an attempt to facilitate sample collection and detect any cross-reactions, the BR dipstick was used to screen blood spots, that had been allowed to dry on filter paper, for B. timori microfilariae, before the dipstick-positive samples were tested with a PCR-based assay. Of the 66 individuals so tested, 37 (56%) were found positive by the BR test used on dry blood spots and eight (22%) by the filtration of fresh blood samples. Only nine of the 37 dipstick-positive samples were found PCR-positive. The combined use of BR tests and PCR-based assays, for testing blood spots in areas where brugian filariasis is endemic, appears to be a promising method not only for post-treatment monitoring but also for the certification activities planned within the framework of the Global Programme to Eliminate Lymphatic Filariasis.
机译:建立简单,敏感和特定的工具来诊断比利时淋巴丝虫病是成功干预以控制该疾病的前提。在简单快速的布鲁吉亚快速(BR)测试中,使用了一种免疫色谱试纸来检测与重组马来西亚布鲁吉亚抗原具有反应性的IgG(4)抗体。当使用BR检验对109名患有布鲁氏微丝虫病的个体(其中B. malayi为12例,B。timori为97例)的血清进行检查时,所有患者的血清均为阳性。相反,在BR试验中发现被调查的Onchocerca volvulus或Mansonella感染个体的所有150份血清均为阴性。但是,观察到与班氏Wuchereria bancrofti(12个测试阳性中的3个)和Dirofilaria(9个测试阳性中的一个)感染的个体的血清有一些不受欢迎的交叉反应。为了促进样品收集和检测到任何交叉反应,在用DIP试纸阳性样品进行检测之前,使用BR试纸来筛查血滴(已使其在滤纸上干燥)以检测timori B. timori微丝aria。基于PCR的检测。在如此测试的66个人中,通过对干血斑进行的BR试验发现37个人(56%)为阳性,通过新鲜血液样品的过滤发现8个人(22%)。在37个量油尺阳性样本中,只有9个被PCR阳性。结合使用BR试验和基于PCR的试验来检测布鲁氏丝虫病流行地区的血斑,这不仅是治疗后监测的一种有前途的方法,而且对于在全球框架内计划进行的认证活动也是一种有前途的方法消除淋巴丝虫病的计划。

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