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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSM69765"><item key="DISEASE STATE">HIV-</item></item></item><item><item key="GSM69765"><item key="DISEASE STATE">HIV-</item></item></item><item><item key="GSM69765"><item key="DISEASE STATE">HIV-</item></item></item><item><item key="GSM697654"><item key="DISEASE STATE">HIV+</item></item></item><item><item key="GSM697654"><item key="DISEASE STATE">HIV+</item></item></item><item><item key="GSM697654"><item key="DISEASE STATE">HIV+</item></item></item></item><item key="id">4015</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">We evaluated longitudinal changes in viral replication and emergence of viral variants in the context of T cell homeostasis and gene...</item><item key="geo_gse_id">E-GEOD-28177</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>gut</item><item>hiv infection</item><item>longitudinal</item><item>peripheral</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">expression-data-from-haart-interruption-in-hiv-pat</item><item key="geo_id_plat">E-GEOD-28177_A-AFFY-44</item><item key="name">Expression data from HAART interruption in HIV patients</item><item key="created">Sep.16, 2014</item><item key="summary">We evaluated longitudinal changes in viral replication and emergence of viral variants in the context of T cell homeostasis and gene expression in GALT of three HIV-positive patients who initiated HAART during primary HIV infection but opted to interrupt therapy thereafter. Longitudinal viral sequence analysis revealed that a stable proviral reservoir was established in GALT during primary HIV infection that persisted through early HAART and post-therapy interruption. Proviral variants in GALT and peripheral blood mononuclear cells (PBMCs) displayed low levels of genomic diversity at all times. A rapid increase in viral loads with a modest decline of CD4  T cells in peripheral blood was observed, while gut mucosal CD4 T cell loss was severe following HAART interruption. This was accompanied by increased mucosal gene expression regulating interferon (IFN)-mediated antiviral responses and immune activation, a profile similar to those found in HAART-naive HIV-infected patients. Gut mucosal responses to HAART interruption were evaluated with Affymetrix arrays</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-28177</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-28177/samples/</item></data></biogps>
