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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="id">3102</item><item key="factors"><item><item key="GSE13738GSM345232"/></item><item><item key="GSE13738GSM345246"/></item><item><item key="GSE13738GSM345250"/></item><item><item key="GSE13738GSM345259"/></item><item><item key="GSE13738GSM345264"/></item><item><item key="GSE13738GSM345266"/></item><item><item key="GSE13738GSM345267"/></item><item><item key="GSE13738GSM345280"/></item><item><item key="GSE13738GSM345281"/></item><item><item key="GSE13738GSM345282"/></item><item><item key="GSE13738GSM345283"/></item><item><item key="GSE13738GSM345284"/></item></item><item key="pop_total">0</item><item key="platform">4</item><item key="summary_wrapped">There is much evidence that T cells may be activated via mechanisms which act independently of direct TCR ligation. Despite this, the...</item><item key="pubmed_id">19201849</item><item key="geo_gse_id">E-GEOD-13738</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">12</item><item key="tags"><item>cell</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-13738_A-AFFY-44</item><item key="slug">transcription-profiling-of-human-cd4-memory-t-cell</item><item key="geo_gds_id"/><item key="name">Transcription profiling of human CD4+ memory T cells reveals they are preferential targets for bystander activation and apoptosis</item><item key="created">Sep.11, 2014</item><item key="summary">There is much evidence that T cells may be activated via mechanisms which act independently of direct TCR ligation. Despite this, the question of whether such forms of &#8216;bystander&#8217; T cell activation occur during immune responses is hotly debated.  To address some outstanding questions, we set up an in vitro system within which to analyse bystander T cell activation in human T cells, in the absence of the possibility for TCR cross-reactivity. In addition, we have investigated the genetic, phenotypic, and functional characteristics of bystander activated T cells.   Here, we show that bystander T cell activation is, indeed, observed during a specific immune response, and that it occurs preferentially amongst CD4+ memory T cells. Furthermore, bystander activated T cells display a distinct gene expression profile. The mechanism for bystander T cell activation involves soluble factors, and the outcome is an elevated level of apoptosis. This may provide an explanation for the attrition of T cell memory pools of heterologous specificity during immune responses to pathogens such as viruses. Experiment Overall Design: Three conditions tested with 4 biological repilicates in each: Experiment Overall Design:   Resting cells - cells expressing a TCR which does not specifically recognize SEB (V&#946;13.1 T cells) and did not upregulate the activation marker CD25 in response to transwell SEB-stimulated co-culture over a 5 day period. Experiment Overall Design:   Bystander activated cells - cells expressing a TCR which does not specifically recognize SEB (V&#946;13.1 T cells), but which did upregulate the activation marker CD25 in response to transwell SEB-stimulated co-culture over a 5 day period. Experiment Overall Design:   Directly activated cells - cells expressing a TCR which is known to specifically recognize SEB (V&#946;17 T cells), and which did upregulate the activation marker CD25 in response to direct SEB stimulation over a 5 day period.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-13738</item><item key="species">human</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-13738/samples/</item></data></biogps>
