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Antigens of Tumours Induced by Naturally Occurring Murine Sarcoma Virus (MSV-FBJ): I. Detection of Group and Type Specific Antigens by Complement Fixation

Antigens associated with cells transformed in vivo by FBJ virus, a wild type murine sarcoma virus (MSV) complex originating from a spontaneously arising osteosarcoma in a CF1 mouse, have been partially characterized by complement fixation (CF). Using rat antisera against antigens specified by Gross...

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Detalles Bibliográficos
Autores principales: Jones, D. B., Moore, M.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1974
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009148/
https://www.ncbi.nlm.nih.gov/pubmed/4820943
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author Jones, D. B.
Moore, M.
author_facet Jones, D. B.
Moore, M.
author_sort Jones, D. B.
collection PubMed
description Antigens associated with cells transformed in vivo by FBJ virus, a wild type murine sarcoma virus (MSV) complex originating from a spontaneously arising osteosarcoma in a CF1 mouse, have been partially characterized by complement fixation (CF). Using rat antisera against antigens specified by Gross leukaemia virus (GLV) the group specific (gs) antigen of C-type RNA murine tumour viruses was demonstrated in FBJ tumours as well as in GLV rat leukaemias, AKR lymphomata and sarcomata induced by MSV-H (Harvey), an MSV isolate of Friend-Moloney-Rauscher (FMR) subgroup specificity. Using mouse antisera against antigens present in FBJ cells the Gross (G) or wild type specificity of FBJ tumours was demonstrated by cross reactivity with antigens expressed on normal AKR lymphoid tissues and leukaemias. These antigens were absent from MSV-H induced sarcomata and in reciprocal tests mouse antisera to MSV-H failed to react with antigens present in FBJ tumour cells. No distinction between cellular and virion antigens expressed by FBJ cells was possible by CF although evidence for a cellular antigen with G specificity was obtained in tests using aged C57B1 antiserum containing a naturally occurring G antibody lacking significant virus neutralizing capacity. However, the likelihood that mouse FBJ antisera contain antibodies to type specific viral envelope antigens (VEA) as well as cellular antigen is discussed.
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spelling pubmed-20091482009-09-10 Antigens of Tumours Induced by Naturally Occurring Murine Sarcoma Virus (MSV-FBJ): I. Detection of Group and Type Specific Antigens by Complement Fixation Jones, D. B. Moore, M. Br J Cancer Articles Antigens associated with cells transformed in vivo by FBJ virus, a wild type murine sarcoma virus (MSV) complex originating from a spontaneously arising osteosarcoma in a CF1 mouse, have been partially characterized by complement fixation (CF). Using rat antisera against antigens specified by Gross leukaemia virus (GLV) the group specific (gs) antigen of C-type RNA murine tumour viruses was demonstrated in FBJ tumours as well as in GLV rat leukaemias, AKR lymphomata and sarcomata induced by MSV-H (Harvey), an MSV isolate of Friend-Moloney-Rauscher (FMR) subgroup specificity. Using mouse antisera against antigens present in FBJ cells the Gross (G) or wild type specificity of FBJ tumours was demonstrated by cross reactivity with antigens expressed on normal AKR lymphoid tissues and leukaemias. These antigens were absent from MSV-H induced sarcomata and in reciprocal tests mouse antisera to MSV-H failed to react with antigens present in FBJ tumour cells. No distinction between cellular and virion antigens expressed by FBJ cells was possible by CF although evidence for a cellular antigen with G specificity was obtained in tests using aged C57B1 antiserum containing a naturally occurring G antibody lacking significant virus neutralizing capacity. However, the likelihood that mouse FBJ antisera contain antibodies to type specific viral envelope antigens (VEA) as well as cellular antigen is discussed. Nature Publishing Group 1974-01 /pmc/articles/PMC2009148/ /pubmed/4820943 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Articles
Jones, D. B.
Moore, M.
Antigens of Tumours Induced by Naturally Occurring Murine Sarcoma Virus (MSV-FBJ): I. Detection of Group and Type Specific Antigens by Complement Fixation
title Antigens of Tumours Induced by Naturally Occurring Murine Sarcoma Virus (MSV-FBJ): I. Detection of Group and Type Specific Antigens by Complement Fixation
title_full Antigens of Tumours Induced by Naturally Occurring Murine Sarcoma Virus (MSV-FBJ): I. Detection of Group and Type Specific Antigens by Complement Fixation
title_fullStr Antigens of Tumours Induced by Naturally Occurring Murine Sarcoma Virus (MSV-FBJ): I. Detection of Group and Type Specific Antigens by Complement Fixation
title_full_unstemmed Antigens of Tumours Induced by Naturally Occurring Murine Sarcoma Virus (MSV-FBJ): I. Detection of Group and Type Specific Antigens by Complement Fixation
title_short Antigens of Tumours Induced by Naturally Occurring Murine Sarcoma Virus (MSV-FBJ): I. Detection of Group and Type Specific Antigens by Complement Fixation
title_sort antigens of tumours induced by naturally occurring murine sarcoma virus (msv-fbj): i. detection of group and type specific antigens by complement fixation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009148/
https://www.ncbi.nlm.nih.gov/pubmed/4820943
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