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Measurement by Leukocyte Adherence Inhibition of Autosensitization of Cancer Patients to Myelin Basic Protein

In vitro cell‐mediated immunity was assayed by leukocyte adherence inhibition (LAI) to determine the extent of autosensitization to myelin basic protein (MBP). Leukocytes from 123 cancer patients, 16 patients freed of cancer, 135 patients with benign disease, and 26 patients with destruction of nerv...

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Detalles Bibliográficos
Autores principales: Gouda, Zinab, Thomson, David M. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917501/
https://www.ncbi.nlm.nih.gov/pubmed/2454907
http://dx.doi.org/10.1111/j.1349-7006.1988.tb01623.x
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author Gouda, Zinab
Thomson, David M. P.
author_facet Gouda, Zinab
Thomson, David M. P.
author_sort Gouda, Zinab
collection PubMed
description In vitro cell‐mediated immunity was assayed by leukocyte adherence inhibition (LAI) to determine the extent of autosensitization to myelin basic protein (MBP). Leukocytes from 123 cancer patients, 16 patients freed of cancer, 135 patients with benign disease, and 26 patients with destruction of nervous parenchyma were tested. Most patients with cancer reacted to MBP: 92%, 93%, 82%, 78%, 75% and 62% for pancreatic, colonic, esophageal, lung, ovarian and breast. Few patients with benign diseases reacted to MBP. Patients with multiple sclerosis (MS) were sensitized to MBP, but patients with other nervous tissue injury did not react to MBP. Cancer patients did not remain sensitized to MBP once they were freed of their cancer. The LAI assay is a straightforward method of measuring cellular autosensitivity to MBP. In the population of patients tested, autosensitivity to MBP was confined, except for MS, principally to cancer patients.
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spelling pubmed-59175012018-05-11 Measurement by Leukocyte Adherence Inhibition of Autosensitization of Cancer Patients to Myelin Basic Protein Gouda, Zinab Thomson, David M. P. Jpn J Cancer Res Article In vitro cell‐mediated immunity was assayed by leukocyte adherence inhibition (LAI) to determine the extent of autosensitization to myelin basic protein (MBP). Leukocytes from 123 cancer patients, 16 patients freed of cancer, 135 patients with benign disease, and 26 patients with destruction of nervous parenchyma were tested. Most patients with cancer reacted to MBP: 92%, 93%, 82%, 78%, 75% and 62% for pancreatic, colonic, esophageal, lung, ovarian and breast. Few patients with benign diseases reacted to MBP. Patients with multiple sclerosis (MS) were sensitized to MBP, but patients with other nervous tissue injury did not react to MBP. Cancer patients did not remain sensitized to MBP once they were freed of their cancer. The LAI assay is a straightforward method of measuring cellular autosensitivity to MBP. In the population of patients tested, autosensitivity to MBP was confined, except for MS, principally to cancer patients. Blackwell Publishing Ltd 1988-04 /pmc/articles/PMC5917501/ /pubmed/2454907 http://dx.doi.org/10.1111/j.1349-7006.1988.tb01623.x Text en
spellingShingle Article
Gouda, Zinab
Thomson, David M. P.
Measurement by Leukocyte Adherence Inhibition of Autosensitization of Cancer Patients to Myelin Basic Protein
title Measurement by Leukocyte Adherence Inhibition of Autosensitization of Cancer Patients to Myelin Basic Protein
title_full Measurement by Leukocyte Adherence Inhibition of Autosensitization of Cancer Patients to Myelin Basic Protein
title_fullStr Measurement by Leukocyte Adherence Inhibition of Autosensitization of Cancer Patients to Myelin Basic Protein
title_full_unstemmed Measurement by Leukocyte Adherence Inhibition of Autosensitization of Cancer Patients to Myelin Basic Protein
title_short Measurement by Leukocyte Adherence Inhibition of Autosensitization of Cancer Patients to Myelin Basic Protein
title_sort measurement by leukocyte adherence inhibition of autosensitization of cancer patients to myelin basic protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917501/
https://www.ncbi.nlm.nih.gov/pubmed/2454907
http://dx.doi.org/10.1111/j.1349-7006.1988.tb01623.x
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