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Enhanced Tumor Localization of Radiolabeled Fab Fragments of Monoclonal Antibody A7 in Nude Mice Bearing Human Pancreatic Carcinoma Xenografts
Much recent research has been directed toward the use of monoclonal antibodies (MAb) for the inimunodetection of solid tumors. In pancreatic cancer, the results of conventional immunoscintigraphy using intact MAb remain disappointing. Clear immunoseintigrapliy with radiolabeled MAb requires a high t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1993
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919260/ https://www.ncbi.nlm.nih.gov/pubmed/8407556 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02066.x |
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author | Otsuji, Eigo Yamaguchi, Toshiharu Yamaoka, Nobuki Kato, Makoto Kotani, Tatsuya Kitamura, Kazuya Yamaguchi, Nozomi Takahashi, Toshio |
author_facet | Otsuji, Eigo Yamaguchi, Toshiharu Yamaoka, Nobuki Kato, Makoto Kotani, Tatsuya Kitamura, Kazuya Yamaguchi, Nozomi Takahashi, Toshio |
author_sort | Otsuji, Eigo |
collection | PubMed |
description | Much recent research has been directed toward the use of monoclonal antibodies (MAb) for the inimunodetection of solid tumors. In pancreatic cancer, the results of conventional immunoscintigraphy using intact MAb remain disappointing. Clear immunoseintigrapliy with radiolabeled MAb requires a high tumor tissue/blood ratio of radioactivity and a low normal tissue/blood ratio of radioactivity. In this study, (125)I‐labeled Fab fragments produced by papain digestion of MAb A7 were injected intravenously into nude mice bearing a human pancreatic cancer (HPC‐YS) xenograft previously shown to react specifically with MAb A7. The radioactivity of tumors and normal organs was subsequently measured. The tumor tissue/blood ratio of (125)I‐labeled Fab fragments of MAb A7 was 1.00±0.24 and 9.68±2.54 at 2 and 24 h after injection, respectively. The tumor tissue/blood ratio of radioactivity was significantly higher than those of normal organs at 24 h after injection. Moreover, the tumor tissue/blood ratio of (125)I‐labeled Fab fragments of MAb A7 was greater than that of intact MAb A7, although the (125)I‐labeled Fab accumulation level was much less than that of (125)I‐labeled intact MAb A7 in the tumor. When mice bearing tumors which did not react with MAb A7 were studied, (125)I‐labeled Fab fragments did not specifically localize to the tumors. These results suggest that Fab fragments of MAb A7 may be suitable carriers of radionuclides for the immunodetection of human pancreatic cancer. |
format | Online Article Text |
id | pubmed-5919260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59192602018-05-11 Enhanced Tumor Localization of Radiolabeled Fab Fragments of Monoclonal Antibody A7 in Nude Mice Bearing Human Pancreatic Carcinoma Xenografts Otsuji, Eigo Yamaguchi, Toshiharu Yamaoka, Nobuki Kato, Makoto Kotani, Tatsuya Kitamura, Kazuya Yamaguchi, Nozomi Takahashi, Toshio Jpn J Cancer Res Article Much recent research has been directed toward the use of monoclonal antibodies (MAb) for the inimunodetection of solid tumors. In pancreatic cancer, the results of conventional immunoscintigraphy using intact MAb remain disappointing. Clear immunoseintigrapliy with radiolabeled MAb requires a high tumor tissue/blood ratio of radioactivity and a low normal tissue/blood ratio of radioactivity. In this study, (125)I‐labeled Fab fragments produced by papain digestion of MAb A7 were injected intravenously into nude mice bearing a human pancreatic cancer (HPC‐YS) xenograft previously shown to react specifically with MAb A7. The radioactivity of tumors and normal organs was subsequently measured. The tumor tissue/blood ratio of (125)I‐labeled Fab fragments of MAb A7 was 1.00±0.24 and 9.68±2.54 at 2 and 24 h after injection, respectively. The tumor tissue/blood ratio of radioactivity was significantly higher than those of normal organs at 24 h after injection. Moreover, the tumor tissue/blood ratio of (125)I‐labeled Fab fragments of MAb A7 was greater than that of intact MAb A7, although the (125)I‐labeled Fab accumulation level was much less than that of (125)I‐labeled intact MAb A7 in the tumor. When mice bearing tumors which did not react with MAb A7 were studied, (125)I‐labeled Fab fragments did not specifically localize to the tumors. These results suggest that Fab fragments of MAb A7 may be suitable carriers of radionuclides for the immunodetection of human pancreatic cancer. Blackwell Publishing Ltd 1993-08 /pmc/articles/PMC5919260/ /pubmed/8407556 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02066.x Text en |
spellingShingle | Article Otsuji, Eigo Yamaguchi, Toshiharu Yamaoka, Nobuki Kato, Makoto Kotani, Tatsuya Kitamura, Kazuya Yamaguchi, Nozomi Takahashi, Toshio Enhanced Tumor Localization of Radiolabeled Fab Fragments of Monoclonal Antibody A7 in Nude Mice Bearing Human Pancreatic Carcinoma Xenografts |
title | Enhanced Tumor Localization of Radiolabeled Fab Fragments of Monoclonal Antibody A7 in Nude Mice Bearing Human Pancreatic Carcinoma Xenografts |
title_full | Enhanced Tumor Localization of Radiolabeled Fab Fragments of Monoclonal Antibody A7 in Nude Mice Bearing Human Pancreatic Carcinoma Xenografts |
title_fullStr | Enhanced Tumor Localization of Radiolabeled Fab Fragments of Monoclonal Antibody A7 in Nude Mice Bearing Human Pancreatic Carcinoma Xenografts |
title_full_unstemmed | Enhanced Tumor Localization of Radiolabeled Fab Fragments of Monoclonal Antibody A7 in Nude Mice Bearing Human Pancreatic Carcinoma Xenografts |
title_short | Enhanced Tumor Localization of Radiolabeled Fab Fragments of Monoclonal Antibody A7 in Nude Mice Bearing Human Pancreatic Carcinoma Xenografts |
title_sort | enhanced tumor localization of radiolabeled fab fragments of monoclonal antibody a7 in nude mice bearing human pancreatic carcinoma xenografts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919260/ https://www.ncbi.nlm.nih.gov/pubmed/8407556 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02066.x |
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