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DOI 10.1016/s1386-6532(00)00178-5

Медицинская библиотека · Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2001

Comparison of six different commercial IgG-ELISA kits for the detection of TBEV-antibodies.

Niedrig M, Vaisviliene D, Teichmann A, Klockmann U, Biel S S

Сравнительное исследованиеСтатьяПеревод в очереди

Аннотация

BACKGROUND

Tick-borne encephalitis virus (TBEV) is a pathogenic human flavivirus endemic in some parts of Europe and Asia. Commercial enzyme immunoassays (EIA) for the detection of IgG antibodies are often used in TBEV-seroprevalence studies, as well as for the confirmation of a successful vaccination against TBEV. However, the detection of TBEV-specific antibodies can be biased by the cross-reactivity between different flavivirus genera.

OBJECTIVES

To compare different EIA test systems for the detection of TBEV-IgG antibodies.

STUDY

DESIGN

Six commercial EIA kits for the detection of TBEV-specific antibodies are compared, using serum panels (n=139) of subjects with a documented clinical history (109 sera from TBEV infected patients, 30 sera from people vaccinated against TBEV). For the analysis of possible cross-reactivities, 24 sera from yellow fever vaccinated people and 13 sera positive for Dengue virus-specific antibodies were also included.

RESULTS

The sensitivity of the different TBEV test systems ranges from 73 to 99%. However, when testing the yellow fever and Dengue virus positive specimens, problems with the flavivirus cross- reactivity become obvious, resulting in specificities between 14 and 81%.

CONCLUSIONS

This study shows the necessity of further improvement of the existing TBEV test systems regarding both sensitivity and specificity.

Для цитирования: Niedrig M, Vaisviliene D, Teichmann A, Klockmann U, Biel S S. Comparison of six different commercial IgG-ELISA kits for the detection of TBEV-antibodies.. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 2001. DOI: 10.1016/s1386-6532(00)00178-5.

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