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European seroepidemiology network 2: Standardisation of assays for seroepidemiology of varicella zoster virus.
Authors:Fernando de Ory  José Manuel Echevarría  George Kafatos  Cleo Anastassopoulou  Nick Andrews  Josephine Backhouse  Guy Berbers  Blazena Bruckova  Daniel I Cohen  Hester de Melker  Irja Davidkin  Giovanni Gabutti  Louise M Hesketh  Kari Johansen  Sari Jokinen  Lindsay Jones  Anika Linde  Elisabeth Miller  Jo?l Mossong  Anthony Nardone  Maria Cristina Rota  Andreas Sauerbrei  Fran?ois Schneider  Zahava Smetana  Annedore Tischer  Athanassios Tsakris  Robert Vranckx
Institution:Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain. fory@isciii.es
Abstract:BACKGROUND: The aim of the European Sero-Epidemiology Network (ESEN2) is to harmonise the serological surveillance of vaccine-preventable diseases in Europe. OBJECTIVE: To allow comparison of antibody prevalence in different countries by standardising results into common units. STUDY DESIGN: For varicella zoster virus (VZV), a reference laboratory established a panel of 148 samples, characterised by indirect enzyme-immunoassay (ELISA), indirect immunofluorescence, and complement fixation test. Fifty-seven samples were also studied by the fluorescence antibody to membrane antigen test. The geometric mean of the antibody activity (GMAA) obtained from four ELISA determinations was used to characterise each sample of the panel as positive (GMAA: >100 mIU/ml), equivocal (GMAA: 50-100 mIU/ml) or negative (GMAA: <50 mIU/ml) for antibody to VZV (anti-VZV). Thirteen laboratories, using five different ELISA tests, tested the panel. RESULTS: Agreement with the reference laboratory was above 85% in all cases, and the R(2) values obtained from regression analysis of the quantitative results were always higher than 0.87. Finally, the regression equations could be used to convert national values into a common unitage. CONCLUSION: This study confirmed that results for anti-VZV obtained by different ELISA methods can be converted into common units, enabling the comparison of the seroprevalence profiles obtained in the participant countries.
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