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一种针对人细小病毒样病原体特异性 IgM 的抗体捕获放射免疫测定法的开发与应用。

The development and use of an antibody capture radioimmunoassay for specific IgM to a human parvovirus-like agent.

作者信息

Anderson M J, Davis L R, Jones S E, Pattison J R, Serjeant G R

出版信息

J Hyg (Lond). 1982 Apr;88(2):309-24. doi: 10.1017/s0022172400070169.

Abstract

An IgM-antibody capture radioimmunoassay (MACRIA) was developed for the detection of IgM antibody specific for the human parvovirus-like agent B19. Diagnosis of infection with this agent by either antigen detection or antibody seroconversion had been made by counter-current immunoelectrophoresis (CIE) in 18 cases of aplastic crisis occurring in children with homozygous sickle-cell disease. The MACRIA described here gave positive results in 17 of these 18 cases; in the remaining case only an acute specimen taken from the patient during viraemia and late convalescent specimens taken 184 and 247 days after onset of illness were available. The test was used to investigate 20 further cases of aplastic crisis in which neither viral antigen nor antibody seroconversion could be detected by CIE. Detection of virus-specific IgM permitted diagnosis of infection with this parvovirus-like agent in 17 of these cases. In the remaining three cases only single serum specimens taken late in convalescence, 82 days or more after the onset of symptoms, were available. In addition to these 34 cases of aplastic crisis in which primary infection with this agent was diagnosed by MACRIA, seven cases of apparent 'silent' infection detected by CIE were investigated. The test permitted the discrimination between primary infection and re-exposure to the virus in six of these patients. The use of this assay has added a considerable weight of evidence implicating primary infection with this parvovirus-like agent as an important cause of aplastic crisis in children with sickle-cell disease. Furthermore, MACRIA permits diagnosis of infection when only single serum specimens taken up to ten weeks after infection are available. Thus the use of this test will significantly facilitate the investigation of other clinical syndromes of presumptive infectious aetiology.

摘要

开发了一种IgM抗体捕获放射免疫分析(MACRIA),用于检测针对人细小病毒样病原体B19的特异性IgM抗体。通过逆流免疫电泳(CIE)对18例纯合子镰状细胞病患儿发生再生障碍危象的病例进行了该病原体感染的诊断,诊断依据为抗原检测或抗体血清转化。此处描述的MACRIA在这18例病例中的17例给出了阳性结果;在其余病例中,仅获得了患者病毒血症期间采集的急性期标本以及发病后184天和247天采集的恢复期晚期标本。该检测用于进一步调查20例再生障碍危象病例,CIE无法检测到病毒抗原或抗体血清转化。在其中17例病例中,病毒特异性IgM的检测使得能够诊断出感染了这种细小病毒样病原体。在其余3例病例中,仅获得了症状出现82天或更长时间后恢复期晚期采集的单一血清标本。除了这34例通过MACRIA诊断为该病原体原发性感染的再生障碍危象病例外,还对CIE检测到的7例明显“无症状”感染病例进行了调查。该检测在其中6例患者中能够区分原发性感染和再次接触病毒。该分析方法的应用为原发性感染这种细小病毒样病原体是镰状细胞病患儿再生障碍危象的重要病因提供了大量证据。此外,当仅获得感染后长达十周采集的单一血清标本时,MACRIA也能够诊断感染。因此,该检测的应用将显著促进对其他假定感染病因的临床综合征的调查。

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