Cargando…

Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes.

In this paper we investigate the reactivity pattern of T cells from stomach carcinoma patients against autologous tumour cells. T cells obtained from the tumour environment, tumour-draining lymph nodes and peripheral blood were cloned in 78 patients with stomach cancer and anti-tumour cytotoxic T ly...

Descripción completa

Detalles Bibliográficos
Autores principales: Stulle, K., Vollmers, H. P., Marquardt, P., Müller-Hermelink, H. K.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033682/
https://www.ncbi.nlm.nih.gov/pubmed/7981054
_version_ 1782136890687750144
author Stulle, K.
Vollmers, H. P.
Marquardt, P.
Müller-Hermelink, H. K.
author_facet Stulle, K.
Vollmers, H. P.
Marquardt, P.
Müller-Hermelink, H. K.
author_sort Stulle, K.
collection PubMed
description In this paper we investigate the reactivity pattern of T cells from stomach carcinoma patients against autologous tumour cells. T cells obtained from the tumour environment, tumour-draining lymph nodes and peripheral blood were cloned in 78 patients with stomach cancer and anti-tumour cytotoxic T lymphocytes (CTLs) precursor frequencies were assessed in each sample by using limiting dilution analysis. When tumour-specific CTLs were tested for specific T-cell killing by using only low doses of Interleukin 2 (100 U ml-1), a moderate rate of proliferation frequency of T cells (0.047) and specific cytotoxicity (12%) were observed in lymph node populations. When both IL-2 and autologous tumour cells in mixed lymphocyte tumour cultures (MLTCs) were used for stimulation, a dramatic increase in number (0.1) and in specific lytic activity (46%) could be measured. No effect or specific activity to tumour cells was observed with peripheral blood lymphocytes and tumour-infiltrating lymphocytes.
format Text
id pubmed-2033682
institution National Center for Biotechnology Information
language English
publishDate 1994
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-20336822009-09-10 Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes. Stulle, K. Vollmers, H. P. Marquardt, P. Müller-Hermelink, H. K. Br J Cancer Research Article In this paper we investigate the reactivity pattern of T cells from stomach carcinoma patients against autologous tumour cells. T cells obtained from the tumour environment, tumour-draining lymph nodes and peripheral blood were cloned in 78 patients with stomach cancer and anti-tumour cytotoxic T lymphocytes (CTLs) precursor frequencies were assessed in each sample by using limiting dilution analysis. When tumour-specific CTLs were tested for specific T-cell killing by using only low doses of Interleukin 2 (100 U ml-1), a moderate rate of proliferation frequency of T cells (0.047) and specific cytotoxicity (12%) were observed in lymph node populations. When both IL-2 and autologous tumour cells in mixed lymphocyte tumour cultures (MLTCs) were used for stimulation, a dramatic increase in number (0.1) and in specific lytic activity (46%) could be measured. No effect or specific activity to tumour cells was observed with peripheral blood lymphocytes and tumour-infiltrating lymphocytes. Nature Publishing Group 1994-12 /pmc/articles/PMC2033682/ /pubmed/7981054 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
Stulle, K.
Vollmers, H. P.
Marquardt, P.
Müller-Hermelink, H. K.
Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes.
title Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes.
title_full Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes.
title_fullStr Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes.
title_full_unstemmed Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes.
title_short Human stomach carcinoma-specific T cells derived from the tumour-draining lymph nodes.
title_sort human stomach carcinoma-specific t cells derived from the tumour-draining lymph nodes.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033682/
https://www.ncbi.nlm.nih.gov/pubmed/7981054
work_keys_str_mv AT stullek humanstomachcarcinomaspecifictcellsderivedfromthetumourdraininglymphnodes
AT vollmershp humanstomachcarcinomaspecifictcellsderivedfromthetumourdraininglymphnodes
AT marquardtp humanstomachcarcinomaspecifictcellsderivedfromthetumourdraininglymphnodes
AT mullerhermelinkhk humanstomachcarcinomaspecifictcellsderivedfromthetumourdraininglymphnodes