Activity and safety of DNA plasmids encoding IL-4 and IFN gamma

被引:29
作者
Ishii, KJ
Weiss, WR
Ichino, M
Verthelyi, D
Klinman, DM [1 ]
机构
[1] US FDA, Ctr Biol Evaluat & Res, Div Viral Prod, Retroviral Immunol Sect, Bethesda, MD 20892 USA
[2] USN, Med Res Inst, Malaria Program, Bethesda, MD 20889 USA
关键词
plasmid DNA; DNA vaccine; cytokines; gene therapy;
D O I
10.1038/sj.gt.3300799
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytokine-encoding DNA plasmids can act as 'genetic adjuvants: improving the immune response stimulated by co-administered DNA vaccines. We examined whether plasmids encoding the Th1 cytokine IFN gamma (pIFN gamma) or the Th2 cytokine IL-4 (pIL-4) have long-term effects on immune homeostasis when administered to adult mice, or alter immune maturation in neonates. Both plasmids boosted immunity against a co-administered vaccine, with pIFN gamma promoting the development of a Th1 response (characterized by the production of IgG2a antibodies), and pIL-4 preferentially stimulating a Th2 response (characterized by increased IgG1 antibody production). Both pIFN gamma and pIL-4 influenced the ratio of cells actively secreting Th1 versus Th2 cytokines, consistent with an effect on Th cell maturation. Interestingly, this effect persisted for only a few weeks and was not magnified by repeated plasmid administration. Cytokine-encoding plasmids had no long-term effect on the immune response of newborn or adult mice to subsequent antigenic stimulation, nor did they selectively induce the production of pathogenic anti-DNA autoantibodies. These results suggest cytokine-encoding plasmids may be safe as immune adjuvants.
引用
收藏
页码:237 / 244
页数:8
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