Recruited inflammatory monocytes stimulate antiviral Th1 immunity in infected tissue

被引:144
作者
Iijima, Norifumi [1 ]
Mattei, Lisa M. [1 ]
Iwasaki, Akiko [1 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
关键词
migration; sexually transmitted infection; antigen presentation; HERPES-SIMPLEX-VIRUS; REPLICATION-DEFECTIVE MUTANT; PLASMACYTOID DENDRITIC CELLS; CHEMOKINE RECEPTOR CCR2; REGULATORY T-CELLS; BACTERIAL-INFECTION; BONE-MARROW; BLOOD MONOCYTES; VIRAL-INFECTION; RESPONSES;
D O I
10.1073/pnas.1005201108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Monocytes patrol various tissues for signs of infection and inflammation. Inflammatory monocytes enter peripheral tissues at sites of microbial infection and differentiate into dendritic cells and macrophages. Here, we examined the importance of monocytes in primary mucosal infection with herpes simplex virus 2 (HSV-2), and demonstrate that monocyte-derived APCs are required to elicit IFN-gamma secretion from effector Th1 cells to mediate antiviral protection. However, monocyte-derived APCs were dispensable for the generation of Th1 immunity and for the restimulation of memory Th1 cells during secondary viral challenge. These results demonstrate that distinct APC subsets are dedicated for CD4 T cell priming, elicitation, and memory recall responses to a given viral pathogen within the same mucosal tissue and reveal a specialized role for monocyte-derived APCs in the emergency response to infection.
引用
收藏
页码:284 / 289
页数:6
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