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1.
Euro Surveill ; 21(16)2016 Apr 21.
Article in English | MEDLINE | ID: mdl-27126052

ABSTRACT

The current Zika virus (ZIKV) epidemic in the Americas caused an increase in diagnostic requests in European countries. Here we demonstrate high specificity of the Euroimmun anti-ZIKV IgG and IgM ELISA tests using putative cross-reacting sera of European patients with antibodies against tick-borne encephalitis virus, dengue virus, yellow fever virus and hepatitis C virus. This test may aid in counselling European travellers returning from regions where ZIKV is endemic.


Subject(s)
Autoantibodies/blood , Enzyme-Linked Immunosorbent Assay/methods , Zika Virus Infection/blood , Zika Virus Infection/virology , Zika Virus/classification , Zika Virus/isolation & purification , Environmental Exposure , Europe/epidemiology , Humans , Immunoglobulin G/immunology , Immunoglobulin M/immunology , Prevalence , Reproducibility of Results , Sensitivity and Specificity , Seroepidemiologic Studies , Zika Virus/immunology , Zika Virus Infection/epidemiology
2.
J Clin Virol ; 74: 13-8, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26638144

ABSTRACT

BACKGROUND: Rubella IgG testing is routinely done in prenatal care and seroepidemiological studies. Recently concern was raised that seropositivity rates were decreasing questioning vaccination policies. Manufacturers of rubella IgG assays and authors of seroepidemiological studies use different cut-offs for the definition of seropositivity. As rubella virus circulation is reduced since many years, seronegativity rates might be overestimated using an inappropriate cut-off. OBJECTIVES: Using different cut-off definitions we compared fourteen current rubella IgG immunoassays for sensitivity and qualitative result concordance in samples with low positive or negative haemagglutination inhibition (HI) titre. STUDY DESIGN: 150 clinical samples from patients and health care workers were included in the study. All samples were measured in 14 different rubella IgG immunoassays. Seropositivity was defined using recombinant rubella IgG immunoblot as reference standard. RESULTS: The concordance of qualitative results using the manufacturers cut-off definitions was 56.4% if grey-zone results were analysed separately and 69.8% if grey-zone results were defined as positive. Using universal cut-offs of 10 IU/ml or 15 IU/ml the concordance was 70% and 61.4% respectively. Using the different cut-off definitions up to 71 out of the 124 immunoblot-positive samples tested negative in the immunoassays. The mean coefficient of variation (CV) of quantitative results in positive samples was 51% (range 19-113%). CONCLUSIONS: Determination of rubella immunity by measurement of rubella-IgG in a population with high vaccination coverage with current assays leads to a high number of false negative results. The value of routine rubella antibody testing in countries with high vaccination coverage should be discussed.


Subject(s)
Antibodies, Viral/blood , Immunoassay/methods , Immunoglobulin G/blood , Rubella virus/immunology , Adolescent , Adult , Aged , Child , Child, Preschool , False Negative Reactions , Female , Humans , Male , Middle Aged , Prospective Studies , Sensitivity and Specificity , Seroepidemiologic Studies , Young Adult
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