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Artigo em Russo | MEDLINE | ID: mdl-16758899

RESUMO

The in vitro experiments with immunoglobulin and blood plasma containing hepatitis B virus (HBV) markers, revealed that the control of immunoglobulin preparations for the presence of hepatitis B virus surface antigen (HBsAg), mandatory for Russia, was not sufficiently informative. The neutralization of HBsAg with specific antibodies to the level, not determined by the EIA method, reached not less than 24 ng/ ml in 2 hours of incubation and not less than 49 ng/ml in 24 hours of incubation, which, when evaluated in 1 lU of anti-HBs, was 34.6 +/- 0.9 ng and 70.7 +/- 1.8 ng of HBsAg respectively. The process of the formation of immune complexes depended mainly on the time of incubation of experimental samples and on the antibody--antigen proportion in the system. The neutralization of viruses by antibodies had no influence on the capacity of the polymerase chain reaction to detect HBV DNA.


Assuntos
Produtos Biológicos/análise , Antígenos de Superfície da Hepatite B/análise , Soros Imunes/análise , Imunoglobulinas Intravenosas/análise , Testes de Neutralização/métodos , Complexo Antígeno-Anticorpo , Produtos Biológicos/normas , Hepatite B/prevenção & controle , Anticorpos Anti-Hepatite B/imunologia , Antígenos de Superfície da Hepatite B/imunologia , Humanos , Soros Imunes/imunologia , Técnicas Imunoenzimáticas , Imunoglobulinas Intravenosas/imunologia , Reação em Cadeia da Polimerase , Sensibilidade e Especificidade , Fatores de Tempo
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