Chemokine CXCL10 (IP-10) is sufficient to trigger an immune response to injected antigens in a mouse model

被引:23
|
作者
Krathwohl, MD [1 ]
Anderson, JL [1 ]
机构
[1] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
关键词
chemokine; vaccination; cytotoxic T cell;
D O I
10.1016/j.vaccine.2005.11.032
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The induction of chemokines by interferons might represent a link between innate and adaptive immunity. Whether these induced chemokines might be useful by themselves to induce an immune response is not known. We hypothesized that the interferon-inducible chemokine CXCL 10 could stimulate dendritic cells (DC) to mature and cross-present exogenous antigen to T cells, resulting in a Th1-type immune response. We found that injecting mice with CXCL 10 together with ovalbumin (OVA) as a test antigen was sufficient to produce functional OVA-specific T cells in 7 of 10 mice. Further, using only CXCL 10 and a peptide antigen derived from vaccinia virus, we were able to induce peptide-specific cytotoxic T cells in 4 of 4 mice tested. These cytotoxic T cells protected 9 of 10 mice from subsequent infectious challenge with vaccinia virus. Unlike traditional adjuvants, no side effects were observed in any of the injected mice. We conclude that CXCL 10 co-administration with a variety of antigens may represent a unique strategy of inducing a protective T cell response to a number of pathogens that merits further study. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2987 / 2993
页数:7
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