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PLoS One ; 19(5): e0302865, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38723016

RESUMO

Influenza A viruses (IAVs) continue to pose a huge threat to public health, and their prevention and treatment remain major international issues. Neuraminidase (NA) is the second most abundant surface glycoprotein on influenza viruses, and antibodies to NA have been shown to be effective against influenza infection. In this study, we generated a monoclonal antibody (mAb), named FNA1, directed toward N1 NAs. FNA1 reacted with H1N1 and H5N1 NA, but failed to react with the NA proteins of H3N2 and H7N9. In vitro, FNA1 displayed potent antiviral activity that mediated both NA inhibition (NI) and blocking of pseudovirus release. Moreover, residues 219, 254, 358, and 388 in the NA protein were critical for FNA1 binding to H1N1 NA. However, further validation is necessary to confirm whether FNA1 mAb is indeed a good inhibitor against NA for application against H1N1 and H5N1 viruses.


Assuntos
Anticorpos Monoclonais , Vírus da Influenza A Subtipo H1N1 , Neuraminidase , Neuraminidase/imunologia , Neuraminidase/metabolismo , Neuraminidase/antagonistas & inibidores , Anticorpos Monoclonais/imunologia , Vírus da Influenza A Subtipo H1N1/imunologia , Humanos , Animais , Anticorpos Antivirais/imunologia , Camundongos , Virus da Influenza A Subtipo H5N1/imunologia , Camundongos Endogâmicos BALB C , Antivirais/farmacologia , Proteínas Virais/imunologia , Proteínas Virais/metabolismo , Vírus da Influenza A Subtipo H3N2/imunologia , Subtipo H7N9 do Vírus da Influenza A/imunologia
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