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Protective role of antigenic sites on the envelope protein of Hantaan virus defined by monoclonal antibodies
To investigate the role of Hantaan virus envelope glycoprotein in infection, a panel of monoclonal antibodies (MAbs) was examined in vitro with several serological tests and in vivo by passive transfer experiments in mice. An antigenic site, specific for the inhibition of infected cell focus was det...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087150/ https://www.ncbi.nlm.nih.gov/pubmed/1381911 http://dx.doi.org/10.1007/BF01309700 |
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author | Arikawa, J. Yao, J. -S. Yoshimatsu, K. Takashima, I. Hashimoto, N. |
author_facet | Arikawa, J. Yao, J. -S. Yoshimatsu, K. Takashima, I. Hashimoto, N. |
author_sort | Arikawa, J. |
collection | PubMed |
description | To investigate the role of Hantaan virus envelope glycoprotein in infection, a panel of monoclonal antibodies (MAbs) was examined in vitro with several serological tests and in vivo by passive transfer experiments in mice. An antigenic site, specific for the inhibition of infected cell focus was detected with the focus inhibition neutralization test (FINT), in addition to the neutralization related antigenic sites, which were revealed by the ordinary focus reduction neutralization test (FRNT). Suckling mice were given the MAbs by passive transfer followed by lethal Hantaan virus challenge. All neutralizing MAbs detected by either FRNT or FINT protected all mice from lethal infection, confirming the importance of the antigenic sites as a protective antigen. Mice given non-neutralizing MAbs by passive transfer, however, began to die earlier than the control group; mean time to death (18.2±2.1 to 21.5±2.8 days) being significantly shorter than that of the control group (25.8±1.8, p<0.01, Mann-Whitney,U probability test). Virus titers in brains of mice which died early, were about 10 times higher than those of control mice. These results indicated the early death phenomenon of mice which was mediated by the antivirus antibody. |
format | Online Article Text |
id | pubmed-7087150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-70871502020-03-23 Protective role of antigenic sites on the envelope protein of Hantaan virus defined by monoclonal antibodies Arikawa, J. Yao, J. -S. Yoshimatsu, K. Takashima, I. Hashimoto, N. Arch Virol Original Papers To investigate the role of Hantaan virus envelope glycoprotein in infection, a panel of monoclonal antibodies (MAbs) was examined in vitro with several serological tests and in vivo by passive transfer experiments in mice. An antigenic site, specific for the inhibition of infected cell focus was detected with the focus inhibition neutralization test (FINT), in addition to the neutralization related antigenic sites, which were revealed by the ordinary focus reduction neutralization test (FRNT). Suckling mice were given the MAbs by passive transfer followed by lethal Hantaan virus challenge. All neutralizing MAbs detected by either FRNT or FINT protected all mice from lethal infection, confirming the importance of the antigenic sites as a protective antigen. Mice given non-neutralizing MAbs by passive transfer, however, began to die earlier than the control group; mean time to death (18.2±2.1 to 21.5±2.8 days) being significantly shorter than that of the control group (25.8±1.8, p<0.01, Mann-Whitney,U probability test). Virus titers in brains of mice which died early, were about 10 times higher than those of control mice. These results indicated the early death phenomenon of mice which was mediated by the antivirus antibody. Springer-Verlag 1992 /pmc/articles/PMC7087150/ /pubmed/1381911 http://dx.doi.org/10.1007/BF01309700 Text en © Springer-Verlag 1992 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Papers Arikawa, J. Yao, J. -S. Yoshimatsu, K. Takashima, I. Hashimoto, N. Protective role of antigenic sites on the envelope protein of Hantaan virus defined by monoclonal antibodies |
title | Protective role of antigenic sites on the envelope protein of Hantaan virus defined by monoclonal antibodies |
title_full | Protective role of antigenic sites on the envelope protein of Hantaan virus defined by monoclonal antibodies |
title_fullStr | Protective role of antigenic sites on the envelope protein of Hantaan virus defined by monoclonal antibodies |
title_full_unstemmed | Protective role of antigenic sites on the envelope protein of Hantaan virus defined by monoclonal antibodies |
title_short | Protective role of antigenic sites on the envelope protein of Hantaan virus defined by monoclonal antibodies |
title_sort | protective role of antigenic sites on the envelope protein of hantaan virus defined by monoclonal antibodies |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087150/ https://www.ncbi.nlm.nih.gov/pubmed/1381911 http://dx.doi.org/10.1007/BF01309700 |
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