Utilization of interleukin-2 gene transfer in local immunotherapy of cancer
Jazyk angličtina Země Německo Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
8440741
PubMed Central
PMC12200183
DOI
10.1007/bf01212720
Knihovny.cz E-zdroje
- MeSH
- buňky NK účinky léků fyziologie MeSH
- DNA genetika MeSH
- imunoterapie * MeSH
- interleukin-2 biosyntéza genetika MeSH
- myši inbrední BALB C MeSH
- myši MeSH
- nádorová transformace buněk genetika MeSH
- nádorové buňky kultivované MeSH
- nádory terapie MeSH
- plazmocytom genetika MeSH
- slezina cytologie imunologie MeSH
- transfekce * MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA MeSH
- interleukin-2 MeSH
It has been previously found that local administration of Balb/c plasmacytoma cells transformed and made non-tumorigenic by insertion of the cloned murine interleukin-2 (IL-2) gene induced regressions of a variety of murine tumours including the original Balb/c plasmacytoma X63-Ag8.653 growing in syngeneic mice. The tumour-inhibitory effect of the plasmacytoma cells transformed by IL-2 cDNA and designated as X63-m-IL-2 was due to their high constitutive production of IL-2. Here we show that admixture of syngeneic spleen cells to the X63-m-IL-2 transformants substantially (P < 0.025) increased the antitumour efficacy of the transformants. Balb/c spleen cells co-cultivated with X63-m-IL-2 cells in vitro yielded predominantly Thy 1.2+, CD3+, LFA-1+ lymphocytes, cytolytic for the X63-Ag8.653 plasmacytoma as well as for other murine tumours, including the X63-m-IL-2 target cells.
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