<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>286(24)</volume><submitter>von Rossum A</submitter><funding>Canadian Institutes of Health Research</funding><pubmed_abstract>The nature of inflammatory signals determines the outcome of T cell responses. However, little is known about how inflammatory cytokines provided to human CD8 T cells during activation affects their susceptibility to post-activation cell death. We have examined and compared the effects of the inflammatory cytokine IL-12, as well as the combination of IL-1, IL-6, and IL-23 (IL-1/6/23) on the susceptibility of primary human CD8 T cells to post-activation cell death. Human CD8 T cells activated in the presence of IL-1/6/23 underwent significantly less cell death after activation as compared with those activated in IL-12. This was due to reduced susceptibility to Fas-mediated activation-induced cell death (AICD). Mechanistically, the reduced level of cell death in CD8 T cells activated in IL-1</pubmed_abstract><journal>The Journal of biological chemistry</journal><pagination>21137-44</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3122175</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Inflammatory cytokines determine the susceptibility of human CD8 T cells to Fas-mediated activation-induced cell death through modulation of FasL and c-FLIP(S) expression.</pubmed_title><pmcid>PMC3122175</pmcid><pubmed_authors>von Rossum A</pubmed_authors><pubmed_authors>Choy JC</pubmed_authors><pubmed_authors>Krall R</pubmed_authors><pubmed_authors>Escalante NK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inflammatory cytokines determine the susceptibility of human CD8 T cells to Fas-mediated activation-induced cell death through modulation of FasL and c-FLIP(S) expression.</name><description>The nature of inflammatory signals determines the outcome of T cell responses. However, little is known about how inflammatory cytokines provided to human CD8 T cells during activation affects their susceptibility to post-activation cell death. We have examined and compared the effects of the inflammatory cytokine IL-12, as well as the combination of IL-1, IL-6, and IL-23 (IL-1/6/23) on the susceptibility of primary human CD8 T cells to post-activation cell death. Human CD8 T cells activated in the presence of IL-1/6/23 underwent significantly less cell death after activation as compared with those activated in IL-12. This was due to reduced susceptibility to Fas-mediated activation-induced cell death (AICD). Mechanistically, the reduced level of cell death in CD8 T cells activated in IL-1</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Jun</publication><modification>2025-04-04T21:57:18.86Z</modification><creation>2019-03-27T00:42:57Z</creation></dates><accession>S-EPMC3122175</accession><cross_references><pubmed>21518761</pubmed><doi>10.1074/jbc.m110.197657</doi><doi>10.1074/jbc.M110.197657</doi></cross_references></HashMap>