<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(1)</volume><submitter>van Rensburg IC</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Studies show that B-cells, in addition to producing antibodies and antigen-presentation, are able to produce cytokines as well. These include regulatory cytokines such as IL-10 by regulatory B-cells. Furthermore, a rare regulatory subset of B-cells have the potential to express FasL, which is a death-inducing ligand. This subset of B-cells have a positive role during autoimmune disease, but has not yet been studied during tuberculosis. These FasL-expressing B-cells are induced by bacterial LPS and CpG, thus we hypothesized that this phenotype might be induced during tuberculosis as well.&lt;h4>Methods&lt;/h4>B-cells from participants with TB (at diagnosis and during treatment) and controls were collected, and analyzed by means of real-time PCR and flow cytometry. In addition</pubmed_abstract><journal>Immunity, inflammation and disease</journal><pagination>57-67</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5322165</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>B-cells with a FasL expressing regulatory phenotype are induced following successful anti-tuberculosis treatment.</pubmed_title><pmcid>PMC5322165</pmcid><pubmed_authors>Walzl G</pubmed_authors><pubmed_authors>Loxton AG</pubmed_authors><pubmed_authors>Kleynhans L</pubmed_authors><pubmed_authors>van Rensburg IC</pubmed_authors><pubmed_authors>Keyser A</pubmed_authors></additional><is_claimable>false</is_claimable><name>B-cells with a FasL expressing regulatory phenotype are induced following successful anti-tuberculosis treatment.</name><description>&lt;h4>Introduction&lt;/h4>Studies show that B-cells, in addition to producing antibodies and antigen-presentation, are able to produce cytokines as well. These include regulatory cytokines such as IL-10 by regulatory B-cells. Furthermore, a rare regulatory subset of B-cells have the potential to express FasL, which is a death-inducing ligand. This subset of B-cells have a positive role during autoimmune disease, but has not yet been studied during tuberculosis. These FasL-expressing B-cells are induced by bacterial LPS and CpG, thus we hypothesized that this phenotype might be induced during tuberculosis as well.&lt;h4>Methods&lt;/h4>B-cells from participants with TB (at diagnosis and during treatment) and controls were collected, and analyzed by means of real-time PCR and flow cytometry. In addition</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2025-04-18T19:23:13.623Z</modification><creation>2019-03-26T23:41:24Z</creation></dates><accession>S-EPMC5322165</accession><cross_references><pubmed>28250925</pubmed><doi>10.1002/iid3.140</doi></cross_references></HashMap>