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用酶免疫试验对人类免疫缺陷病毒(HIV)抗原进行定量检测:与其他检测方法及基于核酸序列的1型HIV RNA扩增法的比较

Quantitative detection of human immunodeficiency virus (HIV) antigen by the Enzymun-Test: comparison with alternative assays and nucleic acid sequence-based amplification of HIV type 1 RNA.

作者信息

Weber B, Melchior W, Preiser W, Hess G, Wahl M, Braner J, Doerr H W

机构信息

Institut für Medizinische Virologie, Zentrum der Hygiene, Universitätskliniken Frankfurt am Main, Germany.

出版信息

J Clin Microbiol. 1996 Jun;34(6):1440-7. doi: 10.1128/jcm.34.6.1440-1447.1996.

Abstract

A new modular automated enzyme immunoassay (EIA) (Enzymun-Test HIV Ag: Boehringer Mannheim) for quantitative human immunodeficiency virus (HIV) antigen detection was evaluated by testing a panel of 1,506 serum samples, including seroconversions, dilution series, follow-up samples from patients under antiretroviral therapy, single serum specimens from HIV-seropositive individuals in different stages of infection, potentially cross-reactive samples, and sera from HIV-negative hospitalized patients. The Abbott HIV type 1 (HIV-1) antigen monoclonal antibody assay served as the reference assay, and nucleic acid sequence-based amplification (Organon Teknika) for quantitative amplification of HIV-1 RNA was used for follow-up of patients under antiretroviral chemotherapy. The Boehringer Mannheim and Abbott EIAs showed concordant results for the early detection of HIV antigen in all the seroconversion panels. The follow-up samples from 29 HIV-infected individuals under antiretroviral therapy gave divergent results between both antigen tests. For the detection of HIV antigen in single serum samples from HIV-infected patients in different stages of HIV infection, a higher number of positive samples was detected with the Abbott HIV-1 antigen monoclonal antibody assay in samples from patients in stages II and III of HIV infection. The Enzymun-Test detected three or more positive samples than did the Abbott assay among the samples of patients with AIDS. The concordance on a sample-to-sample basis between the Boehringer Mannheim and Abbott EIAs was 98.6%. The sensitivity of the Enzymun-Test in comparison to the reference assay was 97.2%; the specificity was 98.8%. Although no close correlation could be found between the amount of viral RNA in serum detected by nucleic acid sequence-based amplification and the concentration of HIV antigen, a high HIV-1 RNA copy number was mostly associated with high levels of HIV antigen. In conclusion, the Enzymun-Test permits accurate HIV antigen detection and offers, in contrast to previous assays, the possibility of completely automated detection.

摘要

通过检测1506份血清样本评估了一种用于定量检测人类免疫缺陷病毒(HIV)抗原的新型模块化自动酶免疫测定法(EIA)(酶免疫检测HIV抗原:宝灵曼公司),这些样本包括血清转化样本、稀释系列样本、接受抗逆转录病毒治疗患者的随访样本、处于不同感染阶段的HIV血清阳性个体的单份血清样本、可能发生交叉反应的样本以及HIV阴性住院患者的血清样本。雅培HIV-1抗原单克隆抗体检测作为参考检测方法,基于核酸序列扩增(欧加农公司)用于HIV-1 RNA定量扩增,用于对抗逆转录病毒化疗患者进行随访。宝灵曼和雅培的酶免疫测定法在所有血清转化样本组中对HIV抗原的早期检测结果一致。29例接受抗逆转录病毒治疗的HIV感染个体的随访样本在两种抗原检测之间得出了不同结果。对于检测处于HIV感染不同阶段的HIV感染患者的单份血清样本中的HIV抗原,在HIV感染II期和III期患者的样本中,雅培HIV-1抗原单克隆抗体检测法检测出的阳性样本数量更多。在艾滋病患者样本中,酶免疫检测比雅培检测法多检测出三个或更多阳性样本。宝灵曼和雅培酶免疫测定法在样本间的一致性为98.6%。与参考检测法相比,酶免疫检测的灵敏度为97.2%;特异性为98.8%。虽然基于核酸序列扩增检测的血清中病毒RNA量与HIV抗原浓度之间未发现密切相关性,但高HIV-1 RNA拷贝数大多与高水平的HIV抗原相关。总之,酶免疫检测能够准确检测HIV抗原,并且与以往检测方法不同,它提供了完全自动化检测的可能性。

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