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Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour.
The TATA of two clones from the same murine methylcholanthrene-induced fibrosarcoma have been investigated by immunizing syngeneic mice with irradiated cells of one or both clones and challenging them 14 days later with viable cells. The tumour had been induced in a female backcross CBA mouse hetero...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1984
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976682/ https://www.ncbi.nlm.nih.gov/pubmed/6197985 |
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author | Woodruff, M. F. Ansell, J. D. Hodson, B. A. Micklem, H. S. |
author_facet | Woodruff, M. F. Ansell, J. D. Hodson, B. A. Micklem, H. S. |
author_sort | Woodruff, M. F. |
collection | PubMed |
description | The TATA of two clones from the same murine methylcholanthrene-induced fibrosarcoma have been investigated by immunizing syngeneic mice with irradiated cells of one or both clones and challenging them 14 days later with viable cells. The tumour had been induced in a female backcross CBA mouse heterozygous for the A and B alloenzymes of phosphoglycerate kinase-1 (PGK-1). One clone expressed A and the other B, and both A and B hosts were used in the experiments. Each clone was found to possess strong TATA but there was no demonstrable cross reactivity. The clonal composition of tumours produced by inoculating mice with a mixture of the two clones was profoundly altered by prior immunization with one of them. A second experiment was performed with 3 clones from another tumour; these expressed PGK-1 A, B and AB respectively. Again, there was no evidence of immunological cross reactivity between the A and B clones, but there was some cross reactivity between the A clone and AB clone. These results, coupled with previous observations of changes in the clonal composition of pleoclonal murine fibrosarcomas in culture and on transplantation, suggest that the antigenic specificity of these tumours is less stable than is commonly supposed. |
format | Text |
id | pubmed-1976682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1984 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19766822009-09-10 Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour. Woodruff, M. F. Ansell, J. D. Hodson, B. A. Micklem, H. S. Br J Cancer Research Article The TATA of two clones from the same murine methylcholanthrene-induced fibrosarcoma have been investigated by immunizing syngeneic mice with irradiated cells of one or both clones and challenging them 14 days later with viable cells. The tumour had been induced in a female backcross CBA mouse heterozygous for the A and B alloenzymes of phosphoglycerate kinase-1 (PGK-1). One clone expressed A and the other B, and both A and B hosts were used in the experiments. Each clone was found to possess strong TATA but there was no demonstrable cross reactivity. The clonal composition of tumours produced by inoculating mice with a mixture of the two clones was profoundly altered by prior immunization with one of them. A second experiment was performed with 3 clones from another tumour; these expressed PGK-1 A, B and AB respectively. Again, there was no evidence of immunological cross reactivity between the A and B clones, but there was some cross reactivity between the A clone and AB clone. These results, coupled with previous observations of changes in the clonal composition of pleoclonal murine fibrosarcomas in culture and on transplantation, suggest that the antigenic specificity of these tumours is less stable than is commonly supposed. Nature Publishing Group 1984-01 /pmc/articles/PMC1976682/ /pubmed/6197985 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 | Research Article Woodruff, M. F. Ansell, J. D. Hodson, B. A. Micklem, H. S. Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour. |
title | Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour. |
title_full | Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour. |
title_fullStr | Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour. |
title_full_unstemmed | Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour. |
title_short | Specificity of tumour associated transplantation antigens (TATA) of different clones from the same tumour. |
title_sort | specificity of tumour associated transplantation antigens (tata) of different clones from the same tumour. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976682/ https://www.ncbi.nlm.nih.gov/pubmed/6197985 |
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