Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Chinese Journal of Oncology ; (12): 894-898, 2009.
Article in Chinese | WPRIM | ID: wpr-295211

ABSTRACT

<p><b>OBJECTIVE</b>To study the immunological suppressing effect of recombinant adenovirus vector rAD-mTERT promotor-m4-1BBL (rAD-mTERT) on mouse hepatoma cell line Hepa1-6 cells in co-culture with T lymphocytes.</p><p><b>METHODS</b>Adding recombinant adenovirus rAD, rAD-CMV-m4-1BBL (rAD-CMV) and rAD-mTERT to Hepa1-6 and L929 cells, respectively, to observe the effect of these adenoviruses on growth and apoptosis of these cells in co-culture with T lymphocytes.</p><p><b>RESULTS</b>Adding adenovirus significantly suppressed the growth and slightly increased apoptosis of the two types of cells (P < 0.05). rAD-mTERT promotor-m4-1BBL showed only pro-apoptotic effect on Hepa1-6 cells. When co-cultured with T lymphocytes, rAD-CMV-m4-1BBL showed promoting effect on apoptosis of the cells. Compared with that of T cells pre-co-culture, CD4(+) and CD8(+) T cells were proliferated, and the ratio of CD4/CD8 was significantly reduced (from 1.27 to 1.08).</p><p><b>CONCLUSION</b>Adding the recombinant adenoviruses only suppresses the cell growth, but not promotes their apoptosis. In co-culture with T lymphocytes, recombinant adenovirus vector rAD-mTERT promotor-m4-1BBL can targetingly suppress the growth and induce apoptosis of Hepa1-6 cells. The apoptosis is induced through the immunological killing effect of T lymphocytes.</p>


Subject(s)
Animals , Mice , 4-1BB Ligand , Genetics , Physiology , Adenoviridae , Genetics , Apoptosis , CD4-CD8 Ratio , Cell Line , Cell Line, Tumor , Cell Proliferation , Coculture Techniques , Fibroblasts , Cell Biology , Genetic Vectors , Liver Neoplasms, Experimental , Allergy and Immunology , Pathology , Mice, Inbred C57BL , Promoter Regions, Genetic , Recombinant Proteins , Genetics , T-Lymphocytes , Allergy and Immunology , Telomerase , Genetics , Transfection
SELECTION OF CITATIONS
SEARCH DETAIL