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Malignant Glial Neoplasms: Definition of a Humoral Host Response to Tumor-Associated Antigen(s)
There is increasing evidence that human tumors possess tumor-associated neo-antigens. The host mounts an immunological response to these antigens, as evidenced by the detection of circulating humoral antibodies in a variety of human neoplasia. An indirect immunofluorescent antibody technique was emp...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
1977
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2595517/ https://www.ncbi.nlm.nih.gov/pubmed/333792 |
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author | Sheikh, Khalid M.A. Apuzzo, Michael L.J. Kochsiek, Kim R. Weiss, Martin H. |
author_facet | Sheikh, Khalid M.A. Apuzzo, Michael L.J. Kochsiek, Kim R. Weiss, Martin H. |
author_sort | Sheikh, Khalid M.A. |
collection | PubMed |
description | There is increasing evidence that human tumors possess tumor-associated neo-antigens. The host mounts an immunological response to these antigens, as evidenced by the detection of circulating humoral antibodies in a variety of human neoplasia. An indirect immunofluorescent antibody technique was employed to detect antibodies to tumor-associated antigens in the sera of patients with malignant gliomas. Viable single cell suspensions were used to demonstrate antibodies to surface contents of tumor cells and cell preparations were snap-frozen at −160° C to demonstrate antibodies to cytoplasmic components of tumor cells. After incubation with serum, the preparations were treated with polyvalent sheep antihuman globulin conjugated to isomer-1-fluorescein isothiocyanate, washed, and examined with a Leitz incident fluorescent microscope. Of the 17 sera from histologically proven malignant glial neoplasm patients, 2 (11%) were positive for an autologous surface antibody reaction. Five (23%) of 21 were positive for an autologus cytoplasmic antibody, however, 10 (47%) of 21 of the sera gave a positive reaction for cross-reacting cytoplasmic antibodies when tested with a battery of tumor cells obtained from different patients with malignant glial tumors. No reaction was observed with normal brain tissue. Absorption studies indicated the presence of a tumor-associated antigen. This study demonstrated that certain patients with malignant gliomas possess circulating antibodies to cytoplasmic components of their own tumor cells. The fact that a number of sera cross-reacted with tumor cells obtained from different patients suggests that antigenic cross-reactivity exists between malignant glioma cells from different patients. It is suggested that with further refinement, immunofluorescent detection of antibodies could evolve as a useful diagnostic adjunct in malignant glioma. |
format | Text |
id | pubmed-2595517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1977 |
record_format | MEDLINE/PubMed |
spelling | pubmed-25955172008-12-05 Malignant Glial Neoplasms: Definition of a Humoral Host Response to Tumor-Associated Antigen(s) Sheikh, Khalid M.A. Apuzzo, Michael L.J. Kochsiek, Kim R. Weiss, Martin H. Yale J Biol Med Original Contributions There is increasing evidence that human tumors possess tumor-associated neo-antigens. The host mounts an immunological response to these antigens, as evidenced by the detection of circulating humoral antibodies in a variety of human neoplasia. An indirect immunofluorescent antibody technique was employed to detect antibodies to tumor-associated antigens in the sera of patients with malignant gliomas. Viable single cell suspensions were used to demonstrate antibodies to surface contents of tumor cells and cell preparations were snap-frozen at −160° C to demonstrate antibodies to cytoplasmic components of tumor cells. After incubation with serum, the preparations were treated with polyvalent sheep antihuman globulin conjugated to isomer-1-fluorescein isothiocyanate, washed, and examined with a Leitz incident fluorescent microscope. Of the 17 sera from histologically proven malignant glial neoplasm patients, 2 (11%) were positive for an autologous surface antibody reaction. Five (23%) of 21 were positive for an autologus cytoplasmic antibody, however, 10 (47%) of 21 of the sera gave a positive reaction for cross-reacting cytoplasmic antibodies when tested with a battery of tumor cells obtained from different patients with malignant glial tumors. No reaction was observed with normal brain tissue. Absorption studies indicated the presence of a tumor-associated antigen. This study demonstrated that certain patients with malignant gliomas possess circulating antibodies to cytoplasmic components of their own tumor cells. The fact that a number of sera cross-reacted with tumor cells obtained from different patients suggests that antigenic cross-reactivity exists between malignant glioma cells from different patients. It is suggested that with further refinement, immunofluorescent detection of antibodies could evolve as a useful diagnostic adjunct in malignant glioma. 1977 /pmc/articles/PMC2595517/ /pubmed/333792 Text en |
spellingShingle | Original Contributions Sheikh, Khalid M.A. Apuzzo, Michael L.J. Kochsiek, Kim R. Weiss, Martin H. Malignant Glial Neoplasms: Definition of a Humoral Host Response to Tumor-Associated Antigen(s) |
title | Malignant Glial Neoplasms: Definition of a Humoral Host Response to Tumor-Associated Antigen(s) |
title_full | Malignant Glial Neoplasms: Definition of a Humoral Host Response to Tumor-Associated Antigen(s) |
title_fullStr | Malignant Glial Neoplasms: Definition of a Humoral Host Response to Tumor-Associated Antigen(s) |
title_full_unstemmed | Malignant Glial Neoplasms: Definition of a Humoral Host Response to Tumor-Associated Antigen(s) |
title_short | Malignant Glial Neoplasms: Definition of a Humoral Host Response to Tumor-Associated Antigen(s) |
title_sort | malignant glial neoplasms: definition of a humoral host response to tumor-associated antigen(s) |
topic | Original Contributions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2595517/ https://www.ncbi.nlm.nih.gov/pubmed/333792 |
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