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In vitro Efficacy of Anti‐glial Fibrillary Acidic Protein Monoclonal Antibodies against Human Malignant Glioma Cell Lines

Our studies have confirmed the presence of large concentrations of various intermediate filament proteins (IFPs) in glioma tissue compared to normal brain. This avenue of research was extended to assess the anti‐proliferative activity of anti‐intermediate filament protein monoclonal antibodies (anti...

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Detalles Bibliográficos
Autores principales: Abaza, Mohamed‐Salah I., Narayan, Raj K., Atassi, M. Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921319/
https://www.ncbi.nlm.nih.gov/pubmed/9439685
http://dx.doi.org/10.1111/j.1349-7006.1997.tb00334.x
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author Abaza, Mohamed‐Salah I.
Narayan, Raj K.
Atassi, M. Z.
author_facet Abaza, Mohamed‐Salah I.
Narayan, Raj K.
Atassi, M. Z.
author_sort Abaza, Mohamed‐Salah I.
collection PubMed
description Our studies have confirmed the presence of large concentrations of various intermediate filament proteins (IFPs) in glioma tissue compared to normal brain. This avenue of research was extended to assess the anti‐proliferative activity of anti‐intermediate filament protein monoclonal antibodies (anti‐IFP mAbs)against human glioma cells. In this study, anti‐proliferative activity of glial fibrillary acidic protein monoclonal antibodies (anti‐GFAP mAbs) has been tested in vitro, using glioma cell lines prepared and established from freshly resected brain tumors. One anaplastic astrocytoma (AA), two glioblastoma multiforme (GB(1) and GB(2)) cell lines and three anti‐GFAP mAbs (Bi(2)C(4), B(12)B(4) and B(6)C(6), all IgG(15), kappa) were used. Immunofiuorescence study indicated the ability of anti‐GFAP mAbs to recognize the cell surface of glioma cells and the inhibition study showed that mAb B(12)B(4) inhibited the proliferation of GB(1), (96%), GB(2)(85%)and AA(93%) at a concentration of 3.2x 10(−10)M. mAb B(12)C(4) inhibited the proliferation of GB(1) (95%), GB(2) (86%) and A A (91%) at a concentration of 3.26 X10‐(10)M and mAb B(6)C(5) inhibited the proliferation of GB(1) (75%), GB(2) (75%) and AA (91%) at a concentration of 2.074 X10 (−19)M. Thymidine release assay demonstrated the cytolytic activities of anti‐GFAP mAbs towards these glioma cell lines, and this observation was confirmed by dye exclusion, which indicated the lysis of glioma cells after anti‐GFAP mAbs treatment. Anti‐GFAP mAbs had little effect (<120%) on normal human lymphocyte, liver and intestine cell lines. These results look promising for radioimaging and immunotherapy of human gliomas.
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spelling pubmed-59213192018-05-11 In vitro Efficacy of Anti‐glial Fibrillary Acidic Protein Monoclonal Antibodies against Human Malignant Glioma Cell Lines Abaza, Mohamed‐Salah I. Narayan, Raj K. Atassi, M. Z. Jpn J Cancer Res Article Our studies have confirmed the presence of large concentrations of various intermediate filament proteins (IFPs) in glioma tissue compared to normal brain. This avenue of research was extended to assess the anti‐proliferative activity of anti‐intermediate filament protein monoclonal antibodies (anti‐IFP mAbs)against human glioma cells. In this study, anti‐proliferative activity of glial fibrillary acidic protein monoclonal antibodies (anti‐GFAP mAbs) has been tested in vitro, using glioma cell lines prepared and established from freshly resected brain tumors. One anaplastic astrocytoma (AA), two glioblastoma multiforme (GB(1) and GB(2)) cell lines and three anti‐GFAP mAbs (Bi(2)C(4), B(12)B(4) and B(6)C(6), all IgG(15), kappa) were used. Immunofiuorescence study indicated the ability of anti‐GFAP mAbs to recognize the cell surface of glioma cells and the inhibition study showed that mAb B(12)B(4) inhibited the proliferation of GB(1), (96%), GB(2)(85%)and AA(93%) at a concentration of 3.2x 10(−10)M. mAb B(12)C(4) inhibited the proliferation of GB(1) (95%), GB(2) (86%) and A A (91%) at a concentration of 3.26 X10‐(10)M and mAb B(6)C(5) inhibited the proliferation of GB(1) (75%), GB(2) (75%) and AA (91%) at a concentration of 2.074 X10 (−19)M. Thymidine release assay demonstrated the cytolytic activities of anti‐GFAP mAbs towards these glioma cell lines, and this observation was confirmed by dye exclusion, which indicated the lysis of glioma cells after anti‐GFAP mAbs treatment. Anti‐GFAP mAbs had little effect (<120%) on normal human lymphocyte, liver and intestine cell lines. These results look promising for radioimaging and immunotherapy of human gliomas. Blackwell Publishing Ltd 1997-11 /pmc/articles/PMC5921319/ /pubmed/9439685 http://dx.doi.org/10.1111/j.1349-7006.1997.tb00334.x Text en
spellingShingle Article
Abaza, Mohamed‐Salah I.
Narayan, Raj K.
Atassi, M. Z.
In vitro Efficacy of Anti‐glial Fibrillary Acidic Protein Monoclonal Antibodies against Human Malignant Glioma Cell Lines
title In vitro Efficacy of Anti‐glial Fibrillary Acidic Protein Monoclonal Antibodies against Human Malignant Glioma Cell Lines
title_full In vitro Efficacy of Anti‐glial Fibrillary Acidic Protein Monoclonal Antibodies against Human Malignant Glioma Cell Lines
title_fullStr In vitro Efficacy of Anti‐glial Fibrillary Acidic Protein Monoclonal Antibodies against Human Malignant Glioma Cell Lines
title_full_unstemmed In vitro Efficacy of Anti‐glial Fibrillary Acidic Protein Monoclonal Antibodies against Human Malignant Glioma Cell Lines
title_short In vitro Efficacy of Anti‐glial Fibrillary Acidic Protein Monoclonal Antibodies against Human Malignant Glioma Cell Lines
title_sort in vitro efficacy of anti‐glial fibrillary acidic protein monoclonal antibodies against human malignant glioma cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921319/
https://www.ncbi.nlm.nih.gov/pubmed/9439685
http://dx.doi.org/10.1111/j.1349-7006.1997.tb00334.x
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