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Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody.
Four patients with chronic lymphocytic leukaemia were treated by one or more infusions of polyclonal antibody specific for the immunoglobulin idiotype expressed on their leukaemic cells. The antibody was in the form of IgG from sheep antiserum. Three of the 4 cases showed a significant fall in blood...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1984
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976721/ https://www.ncbi.nlm.nih.gov/pubmed/6722005 |
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author | Gordon, J. Abdul-Ahad, A. K. Hamblin, T. J. Stevenson, F. K. Stevenson, G. T. |
author_facet | Gordon, J. Abdul-Ahad, A. K. Hamblin, T. J. Stevenson, F. K. Stevenson, G. T. |
author_sort | Gordon, J. |
collection | PubMed |
description | Four patients with chronic lymphocytic leukaemia were treated by one or more infusions of polyclonal antibody specific for the immunoglobulin idiotype expressed on their leukaemic cells. The antibody was in the form of IgG from sheep antiserum. Three of the 4 cases showed a significant fall in blood lymphocyte count. On one occasion most of the residual circulating lymphocytes were apparently dead. However on all occasions the cell counts rebounded to near pre-infusion levels within one week. Viable lymphocytes recovered from the blood after infusion always showed evidence of antigenic modulation: a diminished level of surface idiotype in a patched distribution, with an accompanying refractoriness to lysis by anti-idiotype plus complement. When cultured in vitro blood lymphocytes from three of the four patients revealed an appreciable export of idiotypic Ig. These 3 patients showed plasma levels of idiotypic Ig up to 400 micrograms ml-1, reduced by plasma exchange prior to infusion. The fourth patient had a level of less than 4 micrograms ml-1, and was the only one in whom free antibody could be found in the plasma after infusion. These cases demonstrate two major factors which thwart antibody attack on leukaemic cells--extracellular antigen and antigenic modulation--as well as problems relating to sparseness of surface antigen, recruitment of effectors, and exhaustion of effectors. |
format | Text |
id | pubmed-1976721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1984 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19767212009-09-10 Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody. Gordon, J. Abdul-Ahad, A. K. Hamblin, T. J. Stevenson, F. K. Stevenson, G. T. Br J Cancer Research Article Four patients with chronic lymphocytic leukaemia were treated by one or more infusions of polyclonal antibody specific for the immunoglobulin idiotype expressed on their leukaemic cells. The antibody was in the form of IgG from sheep antiserum. Three of the 4 cases showed a significant fall in blood lymphocyte count. On one occasion most of the residual circulating lymphocytes were apparently dead. However on all occasions the cell counts rebounded to near pre-infusion levels within one week. Viable lymphocytes recovered from the blood after infusion always showed evidence of antigenic modulation: a diminished level of surface idiotype in a patched distribution, with an accompanying refractoriness to lysis by anti-idiotype plus complement. When cultured in vitro blood lymphocytes from three of the four patients revealed an appreciable export of idiotypic Ig. These 3 patients showed plasma levels of idiotypic Ig up to 400 micrograms ml-1, reduced by plasma exchange prior to infusion. The fourth patient had a level of less than 4 micrograms ml-1, and was the only one in whom free antibody could be found in the plasma after infusion. These cases demonstrate two major factors which thwart antibody attack on leukaemic cells--extracellular antigen and antigenic modulation--as well as problems relating to sparseness of surface antigen, recruitment of effectors, and exhaustion of effectors. Nature Publishing Group 1984-05 /pmc/articles/PMC1976721/ /pubmed/6722005 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 Gordon, J. Abdul-Ahad, A. K. Hamblin, T. J. Stevenson, F. K. Stevenson, G. T. Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody. |
title | Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody. |
title_full | Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody. |
title_fullStr | Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody. |
title_full_unstemmed | Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody. |
title_short | Mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody. |
title_sort | mechanisms of tumour cell escape encountered in treating lymphocytic leukaemia with anti-idiotypic antibody. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976721/ https://www.ncbi.nlm.nih.gov/pubmed/6722005 |
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