Cutting edge:: Innate immune system discriminates between RNA containing bacterial versus eukaryotic structural features that prime for high-level IL-12 secretion by dendritic cells

被引:96
作者
Koski, GK
Karikó, K
Xu, SW
Weissman, D
Cohen, PA
Czerniecki, B
机构
[1] Univ Penn, Harrison Dept Surg Res, Dept Surg, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Neurosurg Res, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[4] Cleveland Clin Fdn, Surg Res Ctr, Cleveland, OH 44195 USA
关键词
D O I
10.4049/jimmunol.172.7.3989
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
RNA derived from bacterial but not eukaryotic sources, when transfected into human monocyte-derived dendritic cell precursors, induces high-level IL-12 secretion in conjunction with dendritic cell maturation stimuli. In vitro-transcribed mRNA that mimics the structure of bacterial mRNA in the lack of a long 3'-poly(A) tail likewise induces IL-12 secretion, but this property is lost upon efficient enzymatic 3'-polyadenylation. Among other tested RNAs, only polyuridylic acid induced IL-12 p70. This RNA response phenomenon appears biologically distinct from the classically defined response to dsRNA. RNA-transfected APC also polarize T cells in an IL-12-dependent manner toward the IFN-gamma(high)IL-5 low Th1 phenotype, suggesting a link between the detection of appropriately structured RNA and the skewing of immune responses toward those best suited for controlling intracellular microbes. RNA structured to emulate bacterial-patterns constitutes a novel vaccine strategy to engender polarized Th1-type immune responses.
引用
收藏
页码:3989 / 3993
页数:5
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