IL-1 enhances expansion, effector function, tissue localization, and memory response of antigen-specific CD8 T cells

被引:207
作者
Ben-Sasson, Shlomo Z. [1 ,4 ]
Hogg, Alison [2 ]
Hu-Li, Jane [1 ]
Wingfield, Paul [3 ]
Chen, Xi [1 ]
Crank, Michelle [1 ]
Caucheteux, Stephane [1 ]
Ratner-Hurevich, Maya [4 ]
Berzofsky, Jay A. [2 ]
Nir-Paz, Ran [5 ]
Paul, William E. [1 ]
机构
[1] NIAID, Lab Immunol, Bethesda, MD USA
[2] NCI, Vaccine Branch, Ctr Canc Res, Bethesda, MD 20892 USA
[3] NIAMSD, Prot Express Lab, NIH, Bethesda, MD 20892 USA
[4] Hebrew Univ Jerusalem, Lautenberg Ctr Tumor Immunol, Hadassah Med Ctr, IL-91120 Jerusalem, Israel
[5] Hebrew Univ Jerusalem, Dept Clin Microbiol & Infect Dis, Hadassah Med Ctr, IL-91120 Jerusalem, Israel
基金
美国国家卫生研究院;
关键词
ADAPTIVE IMMUNE-RESPONSES; TUMOR-NECROSIS-FACTOR; TRANSENDOTHELIAL MIGRATION; ENDOTHELIAL-CELLS; DIFFERENTIAL EXPRESSION; ENVELOPE GLYCOPROTEIN; CYTOKINE PRODUCTION; DENDRITIC CELLS; VACCINIA VIRUS; CD11C(+) CELLS;
D O I
10.1084/jem.20122006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Here, we show that interleukin-1 (IL-1) enhances antigen-driven CD8 T cell responses. When administered to recipients of OT-I T cell receptor transgenic CD8 T cells specific for an ovalbumin (OVA) peptide, IL-1 results in an increase in the numbers of wild-type but not IL1R1(-/-) OT-I cells, particularly in spleen, liver, and lung, upon immunization with OVA and lipopolysaccharide. IL-1 administration also results in an enhancement in the frequency of antigen-specific cells that are granzyme B+, have cytotoxic activity, and/ or produce interferon gamma (IFN-gamma). Cells primed in the presence of IL-1 display enhanced expression of granzyme B and increased capacity to produce IFN-gamma when rechallenged 2 mo after priming. In three in vivo models, IL-1 enhances the protective value of weak immunogens. Thus, IL-1 has a marked enhancing effect on antigen-specific CD8 T cell expansion, differentiation, migration to the periphery, and memory.
引用
收藏
页码:491 / 502
页数:12
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