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HEALTHY COMPARISON (1-YES)">1</item><item key="USED IN MGUS VS HEALTHY COMPARISON (1-YES)">1</item></item></item><item><item key="GSM571759"><item key="DISEASE STATE">FL</item><item key="USED IN CLL VS HEALTHY COMPARISON (1-YES)">0</item><item key="AGE IN YEARS">68</item><item key="USED IN FL/EMZL VS HEALTHY COMPARISON (1-YES)">1</item><item key="USED IN MGUS VS HEALTHY COMPARISON (1-YES)">0</item></item></item><item><item key="GSM571760"><item key="DISEASE STATE">healthy</item><item key="USED IN CLL VS HEALTHY COMPARISON (1-YES)">0</item><item key="AGE IN YEARS">36</item><item key="USED IN FL/EMZL VS HEALTHY COMPARISON (1-YES)">1</item><item key="USED IN MGUS VS HEALTHY COMPARISON (1-YES)">0</item></item></item></item><item key="id">3759</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">Epidemiological data show that the immune system may control or promote emergence and growth of a neoplastic lymphomatous clone....</item><item key="pubmed_id">21270444</item><item key="geo_gse_id">E-GEOD-23293</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">5</item><item key="sample_count">41</item><item key="tags"><item>cell</item><item>cll</item><item>compartment</item><item>cytokine</item><item>hepatitis</item><item>hepatitis b</item><item>immune system</item><item>intermediate</item><item>lymphoma</item><item>mgus</item><item>myeloma</item><item>peripheral</item><item>proximal</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-23293_A-AFFY-44</item><item key="slug">definition-and-characterization-of-the-systemic-t</item><item key="geo_gds_id"/><item key="name">Definition and characterization of the systemic T cell dysregulation in untreated indolent B cell lymphoma and very early CLL</item><item key="created">Sep.15, 2014</item><item key="summary">Epidemiological data show that the immune system may control or promote emergence and growth of a neoplastic lymphomatous clone. Conversely, systemic lymphomas, especially myeloma and CLL, are associated with clinical immunodeficiency. This prospective controlled study demonstrates substantially reduced circulating T helper cells, predominantly naive CD4+ cells, in patients with non-leukemic follicular and extranodal marginal zone lymphomas, but not in monoclonal gammopathy and early CLL. These numerical changes were correlated with a preactivated phenotype, hyperreactivity in vitro, presenescence, and a Th2 shift of peripheral T helper cells. No prominent alterations were found in the regulatory T cell compartment. Gene expression profiling of in vitro-stimulated CD4+ cells revealed an independent second alteration of T helper cell physiology which was most pronounced in early CLL but also detectable in FL/eMZL. This pattern consisted of downregulation of proximal and intermediate T-cell receptor signaling cascades and globally reduced cytokine secretion. Both types of T cell dysfunction may contribute to significant immunodeficiency in non-leukemic indolent B-cell lymphomas as demonstrated by refractoriness to hepatitis B vaccination. The precise definition of systemic T cell dysfunction serves as the basis to study its prognostic impact, its relationship to the established influence of the lymphoma microenvironment, and its therapeutic manipulation 8 samples from FL/eMZL patients, 7 samples from CLL patients, 5 samples of MGUS patients, 5 MALT, 16 healthy controls</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-23293</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-23293/samples/</item></data></biogps>
