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Mechanism by which antibodies to non-AgB antigens mediate rejection of rat leukaemia cells.
The August and Hooded rat strains are compatible at the major histocompatibility locus (both are AgB5 or Rtlc). Antisera against the minor histocompatibility antigens of Hooded rats were raised by immunizing August rats with grafts of tumours or normal tissue. Such antisera, if transferred to normal...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1980
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010402/ https://www.ncbi.nlm.nih.gov/pubmed/7426344 |
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author | Denham, S. Hooton, J. W. Barfoot, R. K. Alexander, P. Mayol, R. Wrathmell, A. B. |
author_facet | Denham, S. Hooton, J. W. Barfoot, R. K. Alexander, P. Mayol, R. Wrathmell, A. B. |
author_sort | Denham, S. |
collection | PubMed |
description | The August and Hooded rat strains are compatible at the major histocompatibility locus (both are AgB5 or Rtlc). Antisera against the minor histocompatibility antigens of Hooded rats were raised by immunizing August rats with grafts of tumours or normal tissue. Such antisera, if transferred to normal unimmunized August rats, cause them to reject i.v. administered Hooded rat leukemia (HRL) cells within a few hours, and X-irradiated August rats, for whom a graft of HRL is lethal, can survive indefinitely if pretreated with the antiserum. The distribution of 125I-labelled HRL cells in the tissues of August rats was followed at times after their injection, and it was found that, in the presence of antiserum, i.v. administered leukaemic cells are rapidly destroyed in the liver and spleen. The active component of the antiserum is IgG antibody, and its action is independent of the lytic elements of complement. Antibody-mediated splenic and hepatic clearance of the leukaemia cells is unaffected by total-body X-irradiation but reduced by treating the rats with colloidal carbon. The data are consistent with the hypothesis that the rejection of HRL across the histocompatibility barrier studied is, in the presence of antibody, effected by immunophagocytosis. |
format | Text |
id | pubmed-2010402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1980 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20104022009-09-10 Mechanism by which antibodies to non-AgB antigens mediate rejection of rat leukaemia cells. Denham, S. Hooton, J. W. Barfoot, R. K. Alexander, P. Mayol, R. Wrathmell, A. B. Br J Cancer Research Article The August and Hooded rat strains are compatible at the major histocompatibility locus (both are AgB5 or Rtlc). Antisera against the minor histocompatibility antigens of Hooded rats were raised by immunizing August rats with grafts of tumours or normal tissue. Such antisera, if transferred to normal unimmunized August rats, cause them to reject i.v. administered Hooded rat leukemia (HRL) cells within a few hours, and X-irradiated August rats, for whom a graft of HRL is lethal, can survive indefinitely if pretreated with the antiserum. The distribution of 125I-labelled HRL cells in the tissues of August rats was followed at times after their injection, and it was found that, in the presence of antiserum, i.v. administered leukaemic cells are rapidly destroyed in the liver and spleen. The active component of the antiserum is IgG antibody, and its action is independent of the lytic elements of complement. Antibody-mediated splenic and hepatic clearance of the leukaemia cells is unaffected by total-body X-irradiation but reduced by treating the rats with colloidal carbon. The data are consistent with the hypothesis that the rejection of HRL across the histocompatibility barrier studied is, in the presence of antibody, effected by immunophagocytosis. Nature Publishing Group 1980-09 /pmc/articles/PMC2010402/ /pubmed/7426344 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 Denham, S. Hooton, J. W. Barfoot, R. K. Alexander, P. Mayol, R. Wrathmell, A. B. Mechanism by which antibodies to non-AgB antigens mediate rejection of rat leukaemia cells. |
title | Mechanism by which antibodies to non-AgB antigens mediate rejection of rat leukaemia cells. |
title_full | Mechanism by which antibodies to non-AgB antigens mediate rejection of rat leukaemia cells. |
title_fullStr | Mechanism by which antibodies to non-AgB antigens mediate rejection of rat leukaemia cells. |
title_full_unstemmed | Mechanism by which antibodies to non-AgB antigens mediate rejection of rat leukaemia cells. |
title_short | Mechanism by which antibodies to non-AgB antigens mediate rejection of rat leukaemia cells. |
title_sort | mechanism by which antibodies to non-agb antigens mediate rejection of rat leukaemia cells. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010402/ https://www.ncbi.nlm.nih.gov/pubmed/7426344 |
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