Cargando…
Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones
The possibility that a single human tumor may be composed of an heterogeneous population of cells with respect to susceptibility to lysis by autologous CTL clones was investigated by testing six cytolytic clones derived by micromanipulation against the autologous metastatic melanoma, Me28, and again...
Formato: | Texto |
---|---|
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1986
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188019/ https://www.ncbi.nlm.nih.gov/pubmed/3484513 |
_version_ | 1782146310145572864 |
---|---|
collection | PubMed |
description | The possibility that a single human tumor may be composed of an heterogeneous population of cells with respect to susceptibility to lysis by autologous CTL clones was investigated by testing six cytolytic clones derived by micromanipulation against the autologous metastatic melanoma, Me28, and against 31 clones derived from Me28 by cloning in soft agar. Highly significant differences in the lysis of many tumor clones were observed by three of the CTL effectors in comparison with the cytotoxicity achieved on Me28. These results indicate that cloned cellular reagents can detect heterogeneity among cells isolated from the same melanoma, and suggest that the target determinants recognized on the autologous tumor might be differentially expressed on different neoplastic cells. |
format | Text |
id | pubmed-2188019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1986 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21880192008-04-17 Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones J Exp Med Articles The possibility that a single human tumor may be composed of an heterogeneous population of cells with respect to susceptibility to lysis by autologous CTL clones was investigated by testing six cytolytic clones derived by micromanipulation against the autologous metastatic melanoma, Me28, and against 31 clones derived from Me28 by cloning in soft agar. Highly significant differences in the lysis of many tumor clones were observed by three of the CTL effectors in comparison with the cytotoxicity achieved on Me28. These results indicate that cloned cellular reagents can detect heterogeneity among cells isolated from the same melanoma, and suggest that the target determinants recognized on the autologous tumor might be differentially expressed on different neoplastic cells. The Rockefeller University Press 1986-01-01 /pmc/articles/PMC2188019/ /pubmed/3484513 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones |
title | Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones |
title_full | Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones |
title_fullStr | Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones |
title_full_unstemmed | Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones |
title_short | Heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic T lymphocyte clones |
title_sort | heterogeneity of clones from a human metastatic melanoma detected by autologous cytotoxic t lymphocyte clones |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188019/ https://www.ncbi.nlm.nih.gov/pubmed/3484513 |