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1.
Chinese Journal of Applied Physiology ; (6): 343-347, 2008.
Article Dans Chinois | WPRIM | ID: wpr-252773

Résumé

<p><b>AIM</b>To construct recombinant retroviruses expressing anti-CD20 scFv/CD80/CD28/zeta gene and detect its expression in Jurkat cells.</p><p><b>METHOD</b>CD28-zetacDNA were amplified from plasmids pBULLET and inserted into pLNCX vector that contained anti-CD20 scFv/CD80 gene. The recombinant plasmids were transfected into PA 317 cells. Retroviruses were harvested from culture medium of PA 317 cells. Then NIH 3T3 were transfected with retroviruses. Objective gene expression was determined by PCR and FACS. Jurkat cells were transfected with high titer of retroviruses and resistant clones were obtained by G418 selection. Objective mRNA was determined by RT- PCR.</p><p><b>RESULTS</b>The recombinant eukaryotic vector was constructed successfully by PCR and enzyme digestion analysis and objective gene was amplified from NIH 3T3 cells transfected with retroviruses by PCR; FACS showed that objective protein could be expressed in NIH 3T3 cells. Objective gene was amplified from Jurkat cells transfected with retroviruses by RT-PCR.</p><p><b>CONCLUSION</b>Recombinant retrovirus expressing anti-CD20 scFv/CD80/CD28/zeta gene was successfully constructed and objective protein could be expressed in Jurkat cells.</p>


Sujets)
Humains , Antigènes CD20 , Génétique , Métabolisme , Antigène CD80 , Génétique , Métabolisme , Antigène CD28 , Génétique , Métabolisme , Vecteurs génétiques , Fragments Fab d'immunoglobuline , Génétique , Métabolisme , Région variable d'immunoglobuline , Génétique , Métabolisme , Cellules Jurkat , Protéines de fusion recombinantes , Génétique , Métabolisme , Retroviridae , Génétique , Lymphocytes T , Métabolisme , Transfection
2.
Chinese Journal of Hematology ; (12): 111-114, 2007.
Article Dans Chinois | WPRIM | ID: wpr-328364

Résumé

<p><b>OBJECTIVE</b>To construct anti-CD20scFv/CD80/CD28/zeta recombinant gene modified T cells, test its effectiveness of eradicating CD20+ lymphoma cells and provide a probably new approach to tumor adoptive immunotherapy.</p><p><b>METHODS</b>CD28-zeta cDNA were amplified from vector pBULLET and inserted into pLNCX vector that contained anti-CD20scFv/CD80 gene. The recombinant vectors were transduced into PA317 cells and high titer retroviruses were obtained to infect human peripheral blood T lymphocytes. Resistant T cells were obtained by G418 selection at one week. Then transduced T lymphocytes and lymphoma cell lines Daudi Raji were cocultured. The cytotoxicity and cytokine production of transduced T cells were determined by non-radio-activation cytotoxicity assay and ELISA respectively.</p><p><b>RESULTS</b>The recombinant eukaryotic vector was constructed successfully as proved by enzyme digestion analysis and sequencing. These T cells were able to lyse CD20+ target cells and secrete high levels of IL-2 and IFN-gamma in vitro.</p><p><b>CONCLUSION</b>Recombinant gene modified T cells can be constructed successfully. It can specially kill CD20 positive lymphoma cells in vitro.</p>


Sujets)
Humains , Antigènes CD20 , Génétique , Allergie et immunologie , Antigène CD80 , Génétique , Allergie et immunologie , Antigène CD28 , Génétique , Allergie et immunologie , Lignée cellulaire , Cytotoxicité immunologique , Vecteurs génétiques , Immunothérapie adoptive , Plasmides , Génétique , Lymphocytes T , Allergie et immunologie , Métabolisme , Transfection
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