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Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus
We isolated a replication-competent, neurotropic retrovirus (FrC6 virus) and its molecular clone A8 from the NB-tropic Friend murine leukemia virus (FLV) complex. For detection and characterization of the FrC6 and A8 viruses, monoclonal antibodies (MAbs) against the FLV complex were established. Thi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133943/ https://www.ncbi.nlm.nih.gov/pubmed/8578867 http://dx.doi.org/10.1016/0168-1702(95)00066-Y |
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author | Ikeda, Tomio Takase-Yoden, Sayaka Watanabe, Rihito |
author_facet | Ikeda, Tomio Takase-Yoden, Sayaka Watanabe, Rihito |
author_sort | Ikeda, Tomio |
collection | PubMed |
description | We isolated a replication-competent, neurotropic retrovirus (FrC6 virus) and its molecular clone A8 from the NB-tropic Friend murine leukemia virus (FLV) complex. For detection and characterization of the FrC6 and A8 viruses, monoclonal antibodies (MAbs) against the FLV complex were established. Thirty MAbs, each of which reacted with the FLV-producing cell line, were tested for potential neutralizing activities; only two MAbs inhibited the proliferation of the A8 virus. These two MAbs were ineffective or had very weak neutralizing activities toward the non-neurotropic FLV strain clone 57 virus. Further characterization of MAbs by immunoprecipitation revealed that 4 MAbs recognized the envelope protein of the A8 virus. Two of these 4 MAbs recognized the surface glycoprotein gp70, requiring the conformational epitope of the virus for this recognition, while the other two MAbs, which were reactive with the transmembrane protein p15E, were conformation-independent Both of the MAbs against gp70 distinguished neuropathogenic and non-neuropathogenic viruses to some extent, through neutralizing activity or binding activity detected by immunoprecipitation, whereas the two MAbs against p15E reacted with the viruses in a similar manner. Furthermore, one of the MAbs distinguished the viral antigen in the wall of the vacuolation that composes the spongiotic lesion induced by FrC6 viral infection of the brain. |
format | Online Article Text |
id | pubmed-7133943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71339432020-04-08 Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus Ikeda, Tomio Takase-Yoden, Sayaka Watanabe, Rihito Virus Res Research Paper We isolated a replication-competent, neurotropic retrovirus (FrC6 virus) and its molecular clone A8 from the NB-tropic Friend murine leukemia virus (FLV) complex. For detection and characterization of the FrC6 and A8 viruses, monoclonal antibodies (MAbs) against the FLV complex were established. Thirty MAbs, each of which reacted with the FLV-producing cell line, were tested for potential neutralizing activities; only two MAbs inhibited the proliferation of the A8 virus. These two MAbs were ineffective or had very weak neutralizing activities toward the non-neurotropic FLV strain clone 57 virus. Further characterization of MAbs by immunoprecipitation revealed that 4 MAbs recognized the envelope protein of the A8 virus. Two of these 4 MAbs recognized the surface glycoprotein gp70, requiring the conformational epitope of the virus for this recognition, while the other two MAbs, which were reactive with the transmembrane protein p15E, were conformation-independent Both of the MAbs against gp70 distinguished neuropathogenic and non-neuropathogenic viruses to some extent, through neutralizing activity or binding activity detected by immunoprecipitation, whereas the two MAbs against p15E reacted with the viruses in a similar manner. Furthermore, one of the MAbs distinguished the viral antigen in the wall of the vacuolation that composes the spongiotic lesion induced by FrC6 viral infection of the brain. Published by Elsevier B.V. 1995-10 2000-02-25 /pmc/articles/PMC7133943/ /pubmed/8578867 http://dx.doi.org/10.1016/0168-1702(95)00066-Y Text en Copyright © 1995 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Research Paper Ikeda, Tomio Takase-Yoden, Sayaka Watanabe, Rihito Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus |
title | Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus |
title_full | Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus |
title_fullStr | Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus |
title_full_unstemmed | Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus |
title_short | Characterization of monoclonal antibodies recognizing neurotropic Friend murine leukemia virus |
title_sort | characterization of monoclonal antibodies recognizing neurotropic friend murine leukemia virus |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133943/ https://www.ncbi.nlm.nih.gov/pubmed/8578867 http://dx.doi.org/10.1016/0168-1702(95)00066-Y |
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