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Different biodistribution of 99mTc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human.
Biodistribution of chimeric mouse/human monoclonal antibody against non-specific cross-reacting antigen (chNCA Ab) was studied in athymic mice and patients with metastatic bone disease. 99mTc-chNCA Ab showed a high labelling efficiency, stability and also a high binding ratio to human granulocytes....
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074533/ https://www.ncbi.nlm.nih.gov/pubmed/8664114 |
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author | Oriuchi, N. Watanabe, N. Sugiyama, S. Higuchi, T. Imai, K. Yamanaka, H. Hashimoto, M. Kanda, H. Endo, K. |
author_facet | Oriuchi, N. Watanabe, N. Sugiyama, S. Higuchi, T. Imai, K. Yamanaka, H. Hashimoto, M. Kanda, H. Endo, K. |
author_sort | Oriuchi, N. |
collection | PubMed |
description | Biodistribution of chimeric mouse/human monoclonal antibody against non-specific cross-reacting antigen (chNCA Ab) was studied in athymic mice and patients with metastatic bone disease. 99mTc-chNCA Ab showed a high labelling efficiency, stability and also a high binding ratio to human granulocytes. Since NCA showed cross-reactivity with carcinoembryonic antigen (CEA), animal experiments showed that 99mTc-chNCA Ab was accumulated in the xenografted tumour which expressed CEA, suggesting the preserved immunoreactivity of labelled materials. In the clinical study, injected 99mTc-chNCA Ab formed a high molecular weight complex immediately after intravenous administration and was trapped mainly in liver. The first-phase plasma half-life was 6.4 +/- 1.1 min. None of the patients showed adverse reaction or human antimurine or anti-chimeric antibody in their serum. 99mTc-chNCA Ab demonstrated remarkably different biodistribution between patients and the animal model and showed different pharmacokinetics from other murine and chimeric Abs reported previously. For safety HPLC analysis should be performed before clinical radioimmunodetection or radioimmunotherapy by incubating radiolabelled MAb with human serum under strict conditions. IMAGES: |
format | Text |
id | pubmed-2074533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20745332009-09-10 Different biodistribution of 99mTc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human. Oriuchi, N. Watanabe, N. Sugiyama, S. Higuchi, T. Imai, K. Yamanaka, H. Hashimoto, M. Kanda, H. Endo, K. Br J Cancer Research Article Biodistribution of chimeric mouse/human monoclonal antibody against non-specific cross-reacting antigen (chNCA Ab) was studied in athymic mice and patients with metastatic bone disease. 99mTc-chNCA Ab showed a high labelling efficiency, stability and also a high binding ratio to human granulocytes. Since NCA showed cross-reactivity with carcinoembryonic antigen (CEA), animal experiments showed that 99mTc-chNCA Ab was accumulated in the xenografted tumour which expressed CEA, suggesting the preserved immunoreactivity of labelled materials. In the clinical study, injected 99mTc-chNCA Ab formed a high molecular weight complex immediately after intravenous administration and was trapped mainly in liver. The first-phase plasma half-life was 6.4 +/- 1.1 min. None of the patients showed adverse reaction or human antimurine or anti-chimeric antibody in their serum. 99mTc-chNCA Ab demonstrated remarkably different biodistribution between patients and the animal model and showed different pharmacokinetics from other murine and chimeric Abs reported previously. For safety HPLC analysis should be performed before clinical radioimmunodetection or radioimmunotherapy by incubating radiolabelled MAb with human serum under strict conditions. IMAGES: Nature Publishing Group 1996-06 /pmc/articles/PMC2074533/ /pubmed/8664114 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 Oriuchi, N. Watanabe, N. Sugiyama, S. Higuchi, T. Imai, K. Yamanaka, H. Hashimoto, M. Kanda, H. Endo, K. Different biodistribution of 99mTc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human. |
title | Different biodistribution of 99mTc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human. |
title_full | Different biodistribution of 99mTc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human. |
title_fullStr | Different biodistribution of 99mTc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human. |
title_full_unstemmed | Different biodistribution of 99mTc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human. |
title_short | Different biodistribution of 99mTc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human. |
title_sort | different biodistribution of 99mtc-labelled chimeric mouse-human monoclonal antibody between athymic mice model and human. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074533/ https://www.ncbi.nlm.nih.gov/pubmed/8664114 |
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