Chemokine Receptor CCR7 Contributes to a Rapid and Efficient Clearance of Lytic Murine γ-Herpes Virus 68 from the Lung, Whereas Bronchus-Associated Lymphoid Tissue Harbors Virus during Latency

被引:26
作者
Kocks, Jessica R. [1 ]
Adler, Heiko [2 ]
Danzer, Heike [1 ]
Hoffmann, Katharina [1 ]
Jonigk, Danny [3 ]
Lehmann, Ulrich [3 ]
Foerster, Reinhold [1 ]
机构
[1] Hannover Med Sch, Inst Immunol, D-30625 Hannover, Germany
[2] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Clin Cooperat Grp Hematopoiet Cell Transplantat, Inst Mol Immunol, Munich, Germany
[3] Hannover Med Sch, Inst Pathol, D-30625 Hannover, Germany
关键词
BACTERIAL ARTIFICIAL CHROMOSOME; INTESTINAL IMMUNE-SYSTEM; ALPHA-DEFICIENT MICE; EPSTEIN-BARR-VIRUS; T-CELLS; INFECTIOUS-MONONUCLEOSIS; DENDRITIC CELLS; IN-VIVO; GAMMAHERPESVIRUS; TOLERANCE;
D O I
10.4049/jimmunol.0801826
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Murine gamma-herpes virus 68 is a natural rodent pathogen closely related to the human gamma-herpes viruses Kaposi's sarcoma-associated herpes virus and EBV. By intranasally infecting wild-type and CCR7-deficient mice, we investigated whether CCR7 is necessary for viral clearance from the lung and the establishment of latency. We found during the lytic phase of infection that inflammation in lungs of CCR7(-/-) mice was more severe and viral load significantly higher compared with wild-type littermates. In addition, activation of T cells was delayed and clearance of the inflammation was retarded in mutant lungs, demonstrating that CCR7 is necessary for a rapid and efficient immune response. However, for the establishment of splenomegaly and latency, the presence of CCR7 was dispensable. Finally, by microdissecting BALT, we could demonstrate that these ectopic lymphoid structures are a place in the lung where virus resides during latency. The Journal of Immunology, 2009, 182: 6861-6869.
引用
收藏
页码:6861 / 6869
页数:9
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