Tumor site-selective localization of an adoptively transferred T cell line expressing a macrophage lectin

被引:18
作者
Ichii, S [1 ]
Imai, Y [1 ]
Irimura, T [1 ]
机构
[1] UNIV TOKYO,FAC PHARMACEUT SCI,DEPT CANC BIOL & MOL IMMUNOL,BUNKYO KU,TOKYO 113,JAPAN
关键词
experimental lung metastasis; adoptive immunotherapy; cellular trafficking; C-type lectin;
D O I
10.1002/jlb.62.6.761
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CTLL-2 cells were transfected with an expression vector that contained cDNA of a mouse macrophage galactose/N-acetylgalactosamine-specific calcium-type lectin (MMGL) and a stable transfectant (CTL-ML) was established. These cells and mock transfectant cells (CTL-CEP) were labeled with a long-term fluorescent cell tracer, DiI. The labeled cells were intravenously injected into mice that contained established lung metastases produced by OV2944-HM-1 ovarian tumor cells. Analyses with fluorescence microscopy of a series of frozen lung sections from the recipient mice revealed that CTL-ML preferentially accumulated in the lung metastatic nodules, whereas CTL-CEP did not, Time course studies showed that the preferential accumulation was evident 3 days after adoptive transfer. We also found that OV2944-HM-1 cells bound peanut agglutinin and Vicia villosa agglutinin B-4, whose sugar specificity overlaps with the specificity of MMGL. These results suggested that MMGL molecules expressed on CTLL-2 cells contributed to their selective trafficking or retention ill tumor foci possibly through recognition of tumor-associated cell surface carbohydrate antigens. These results also suggested that MMGL could be used for the selective targeting of effector cells in adoptive immunotherapy.
引用
收藏
页码:761 / 770
页数:10
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