GM-CSF transgene expression in the airway allows aerosolized ovalbumin to induce allergic sensitization in mice

被引:206
作者
Stämpfli, MR
Wiley, RE
Neigh, GS
Gajewska, BU
Lei, XF
Snider, DP
Xing, Z
Jordana, M
机构
[1] McMaster Univ, Dept Pathol & Mol Med, Immunol & Infect Programme, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Ctr Gene Therapeut, Hamilton, ON L8N 3Z5, Canada
关键词
airway inflammation; GM-CSF; ovalbumin; eosinophils; mice;
D O I
10.1172/JCI4160
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The purpose of this study was to explore whether repeated exposure to aerosolized ovalbumin (OVA) in the context of local expression of GM-CSF can initiate a Th2-driven, eosinophilic inflammation in the airways. On day -1, Balb/c mice were infected intranasally with an adenovirus construct expressing GM-CSF (Ad/GM-CSF), From day 0 to day 9 mice were exposed daily to an OVA aerosol. Mice exposed to OVA alone did not show any evidence of airway inflammation. Mice receiving both Ad/GM-CSF and aerosolized OVA exhibited marked airway inflammation characterized by eosinophilia and goblet cell hyperplasia. Migration of eosinophils into the airway was preceded by a rise in IL-5 and IL-4. Both IL-5 and class II MHC were critically required to generate airway eosinophilia. After resolution, airway eosinophilia was reconstituted after a single OVA exposure. Flow cytometric analysis of dispersed lung cells revealed an increase in macrophages and dendritic cells expressing B7.1 and B7.2, and expansion of activated (CD69-expressing) CD4 and CD8 T cells in mice exposed to OVA and Ad/GM-CSF, Our data indicate that expression of GMCSF in the airway compartment increases local antigen presentation capacity, and concomitantly facilitates the development of an antigen-specifics, eosinophilic inflammatory response to an otherwise innocuous antigen.
引用
收藏
页码:1704 / 1714
页数:11
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