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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSM677063"><item key="TISSUE">lung, lymphocytes</item></item></item><item><item key="GSM677064"><item key="TISSUE">bronchial lymphnodes, lymphocytes</item></item></item><item><item key="GSM677064"><item key="TISSUE">bronchial lymphnodes, lymphocytes</item></item></item><item><item key="GSM677063"><item key="TISSUE">lung, lymphocytes</item></item></item><item><item key="GSM677064"><item key="TISSUE">bronchial lymphnodes, lymphocytes</item></item></item><item><item key="GSM677063"><item key="TISSUE">lung, lymphocytes</item></item></item></item><item key="id">6366</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">Role for naturally occurring CD4+CD25+Foxp3+ regulatory T cells (nTregs) in counterbalancing this process. Using a transgenic murine...</item><item key="geo_gse_id">E-GEOD-27379</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">6</item><item key="tags"><item>cell</item><item>disease</item><item>influenza</item><item>lung</item><item>lung disease</item><item>lymph</item><item>spleen</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">cd8-t-cell-mediated-lung-inflammation</item><item key="geo_id_plat">E-GEOD-27379_A-AFFY-45</item><item key="name">CD8+ T cell mediated lung inflammation</item><item key="created">Nov.11, 2014</item><item key="summary">Role for naturally occurring CD4+CD25+Foxp3+ regulatory T cells (nTregs) in counterbalancing this process. Using a transgenic murine model for autoimmune-mediated lung disease, we demonstrated that, despite pulmonary inflammation, lung-specific CD8+ T cells can reside quiescently in close proximity to self-antigen. Whereas self-reactive CD8+ T cells in the inflamed lung and lung-draining lymph nodes down-regulated the expression of effector molecules, those located in the spleen appeared to be partly antigen-experienced and displayed a memory-like phenotype. Since ex vivo-reisolated self-reactive CD8+ T cells were very well capable to respond to the antigen in vitro, we investigated a possible contribution of nTregs to the immune control over autoaggressive CD8+ T cells in the lung. We isolated antigen-specifc CD8+ T-cells from lungs and bronchial lymphnodes derived from chronic diseased mice (SPC-HAxCL4), healthy control mice (CL4) and acute influenza infected control mice (CL4+IAV) and perormed mRNA expression profiling of isolated CD8+ T cells. Each group represents a pool of at least n=4 animals. CD8+ T cell type comparison; lung disease state analysis</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-27379</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-27379/samples/</item></data></biogps>
