Abstract | OBJECTIVE: METHODS: CD3AK cells in normal DBA/2 murine splenocytes were induced with anti-CD3 antibody and low dose recombinant interleukin-2 (rIL-2). The P 388 murine leukemia model was induced by i.p. injection of P 388 cells into normal DBA/2 mice. The tumor-bearing mice were administrated with adoptively transferred CD3AK Cells and/or CTX and/or KSC. RESULTS: After tumor inoculation, the cellular immune function of P 388-bearing mice was supressed markedly. Adoptive transfer of CD3AK cells with low dose rIL-2 into the P 388 mice significantly enhanced the splenocyte proliferation (SP) induced by Con A, the NK cell activity and the splenocytic IL-2 production and prolonged their survival (45.19%); CTX (200 mg/kg) alone prolonged the survival of P 388-bearing mice (29.90%), but further decreased the immunodeficiency; combination of CTX and CD3AK passive transfer could prevent the reduction of SP, NK activity and IL-2 production in the leukemic mice and prolonged the survival (59.45%), combination of KSC and adoptively transfected CD2AK cells and/or CTX had a much better therapeutic efficacy for P 388 murine leukemia, 12.50%-75.00% of the leukemic mice were cured. CONCLUSION:
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Authors | H Wei, L Ma |
Journal | Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
(Zhonghua Xue Ye Xue Za Zhi)
Vol. 18
Issue 5
Pg. 243-6
(May 1997)
ISSN: 0253-2727 [Print] China |
PMID | 15622755
(Publication Type: Journal Article)
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Chemical References |
- CD3 Complex
- Interleukin-2
- Organoselenium Compounds
- kappa-selenocarrageenan
- Cyclophosphamide
- Carrageenan
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Topics |
- Adoptive Transfer
- Animals
- CD3 Complex
(metabolism)
- Carrageenan
(therapeutic use)
- Cell Line, Tumor
- Cells, Cultured
- Cyclophosphamide
(therapeutic use)
- Humans
- Interleukin-2
(biosynthesis)
- Killer Cells, Natural
(immunology)
- Leukemia P388
(drug therapy, immunology, metabolism, therapy)
- Male
- Mice
- Organoselenium Compounds
(therapeutic use)
- Survival Analysis
- Treatment Outcome
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