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检测丝虫特异性IgG4抗体和丝虫DNA,用于帝汶布鲁线虫血斑筛查。

Detection of filaria-specific IgG4 antibodies and filarial DNA, for the screening of blood spots for Brugia timori.

作者信息

Fischer P, Bonow I, Supali T, Rückert P, Rahmah N

机构信息

Department of Helminthology, Bernhard Nocht Institute for Tropical Medicine, Bernhard-Nocht-Strasse 74, D-20359 Hamburg, Germany.

出版信息

Ann Trop Med Parasitol. 2005 Jan;99(1):53-60. doi: 10.1179/136485905X13339.

Abstract

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.

摘要

建立简单、灵敏且特异的工具用于诊断布鲁氏淋巴丝虫病,是成功开展疾病控制干预措施的前提条件。在简单快速的布鲁氏快速(BR)检测中,免疫层析试纸条用于检测与重组马来布鲁线虫抗原发生反应的IgG(4)抗体。当使用BR检测对109例布鲁氏微丝蚴血症患者(12例感染马来布鲁线虫,97例感染帝汶布鲁线虫)的血清进行检测时,所有患者均呈阳性。相比之下,对150例盘尾丝虫或曼氏裂头绦虫感染患者的血清进行BR检测,结果均为阴性。然而,观察到一些不良交叉反应,即感染班氏吴策线虫的患者血清(12例中有3例检测呈阳性)和感染恶丝虫的患者血清(9例中有1例检测呈阳性)。为便于样本采集并检测交叉反应,在用基于PCR的检测方法对试纸条检测呈阳性的样本进行检测之前,先使用BR试纸条对滤纸上干燥的血斑进行帝汶布鲁线虫微丝蚴筛查。在接受检测的66例个体中,用BR检测法检测干燥血斑时,37例(56%)呈阳性,用新鲜血液样本过滤法检测时,8例(22%)呈阳性。在37例试纸条检测呈阳性的样本中,只有9例经PCR检测呈阳性。在布鲁氏丝虫病流行地区,联合使用BR检测和基于PCR的检测方法检测血斑,似乎不仅是治疗后监测的一种有前景的方法,也是全球消除淋巴丝虫病规划框架内计划开展的认证活动的一种有前景的方法。

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