Abstract |
The cytotoxicity of freshly obtained human peripheral blood lymphocytes and lymphocytes activated with human recombinant interleukin II (rIL-2) was evaluated against lung cancer cell lines by the human tumor clonogenic assay. Colony formation of all human lung cancer cell lines, PC-1, 3, 6, 7, 9, 13 and 14 were suppressed by lymphocytes activated with 100 units/ml of human rIL-2 for 72 hr. However, the degree of the suppression of colony formation by lymphocytes activated with rIL-2 was different for each cell line. The per cent inhibition of colony formation obtained by HTCA correlated well with the per cent cytolysis obtained by 51Cr-release assay for all cell lines. HTCA provides a very useful tool for the detection of cytotoxicity of lymphocytes against clonogenic tumor cells.
|
Authors | J Fujita, N Saijo, Y Sasaki, H Futami, J Ishihara, H Takahashi, A Hoshi, A W Hamburger |
Journal | European journal of cancer & clinical oncology
(Eur J Cancer Clin Oncol)
Vol. 22
Issue 4
Pg. 445-50
(Apr 1986)
ISSN: 0277-5379 [Print] England |
PMID | 3488219
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
|
Topics |
- Cell Division
- Cell Line
- Cytotoxicity, Immunologic
- Humans
- Interleukin-2
(immunology)
- Killer Cells, Natural
(immunology)
- Lung Neoplasms
(immunology, pathology)
- Lymphocyte Activation
- Tumor Stem Cell Assay
|