白细胞介素2受体
细胞毒性T细胞
白细胞介素21
FOXP3型
生物
免疫学
CD8型
细胞因子
细胞生物学
效应器
T细胞
免疫系统
抗原提呈细胞
体外
生物化学
作者
Sven Mostböck,M. E. Christine Lutsiak,Diane E. Milenic,Kwamena E. Baidoo,Jeffrey Schlom,Helen Sabzevari
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2008-04-01
卷期号:180 (7): 5118-5129
被引量:36
标识
DOI:10.4049/jimmunol.180.7.5118
摘要
IL-2 is well described as a cytokine with two markedly distinct functionalities: as a necessary signal during CD4(+) and CD8(+) T cell activation/expansion and as an essential cytokine for the maintenance of CD4(+)CD25(+)FoxP3(+) T cells (regulatory T (T(REG)) cells) during homeostasis. In this study we demonstrate for the first time that, compared with the use of IL-2 alone, a complex of IL-2 and anti-IL-2 Ab (IL-2 complex) enhances the effectiveness of a viral vaccine in a mouse model with known Ag specificity. IL-2 complex led to an increase in the number of Ag-specific effector/memory CD8(+) T cells, cytokine production, and CTL lysis following Ag-specific restimulation in a vaccination setting. Our results further demonstrate that this effect is temporary and declines over the course of a few days after the IL-2 complex treatment cycle. Moreover, in contrast to the use of IL-2 alone, IL-2 complex greatly increased the ratio of effector/memory CD8(+) T cells to T(REG) cells. This phenomenon can thus potentially be used in the enhancement of immune responses to vaccination.
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