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1.
Chinese Journal of Biotechnology ; (12): 593-604, 2020.
Artigo em Chinês | WPRIM | ID: wpr-827009

RESUMO

An epidemic of acute respiratory syndrome in humans, which appeared in Wuhan, China in December 2019, was caused by a novel coronavirus (SARS-CoV-2). This disease was named as "Coronavirus Disease 2019" (COVID-19). SARS-CoV-2 was first identified as an etiological pathogen of COVID-19, belonging to the species of severe acute respiratory syndrome-related coronaviruses (SARSr-CoV). The speed of both the geographical transmission and the sudden increase in numbers of cases is much faster than SARS and Middle East respiratory syndrome (MERS). COVID-19 is the first global pandemic caused by a coronavirus, which outbreaks in 211 countries/territories/areas. The vaccine against COVID-19, regarded as an effective prophylactic strategy for control and prevention, is being developed in about 90 institutions worldwide. The experiences and lessons encountered in the previous SARS and MERS vaccine research can be used for reference in the development of COVID-19 vaccine. The present paper hopes to provide some insights for COVID-19 vaccines researchers.


Assuntos
Humanos , Betacoronavirus , Alergia e Imunologia , Pesquisa Biomédica , Infecções por Coronavirus , Epidemiologia , Alergia e Imunologia , Virologia , Internacionalidade , Coronavírus da Síndrome Respiratória do Oriente Médio , Alergia e Imunologia , Pandemias , Pneumonia Viral , Epidemiologia , Alergia e Imunologia , Virologia , Coronavírus Relacionado à Síndrome Respiratória Aguda Grave , Alergia e Imunologia , Síndrome Respiratória Aguda Grave , Alergia e Imunologia , Vacinas Virais , Alergia e Imunologia
2.
Journal of Veterinary Science ; : e68-2020.
Artigo | WPRIM | ID: wpr-833681

RESUMO

A fluorescent microsphere-based immunochromatographic strip test (FICT) was developed for the rapid, sensitive, and quantitative detection of porcine reproductive and respiratory syndrome virus (PRRSV) antibodies at the pen-side. The assay was based on the formation of a sandwich immune-complex (anti-pig IgG-PRRSV antibodies-NSP7/N), which was validated by a comparison with IDEXX-ELISA using 3325 clinical specimens. The diagnostic specificity, sensitivity, and accuracy of FICT were 97.28, 93.41, and 94.95%, respectively. FICT showed a good correlation with the virus neutralization assay. Overall, a promising pen-side diagnostic tool was developed for the rapid and quantitative detection of PRRSV antibodies within 15 min.

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