<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Peng Z</submitter><funding>Scientific Research Foundation of Hunan Provincial Education Department</funding><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Hunan Province</funding><pagination>186</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9281140</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Depression is a recurrent and devastating mental disease that is highly prevalent worldwide. Prolonged exposure to stressful events or a stressful environment is detrimental to mental health. In recent years, an inflammatory hypothesis has been implicated in the pathogenesis of stress-induced depression. However, less attention has been given to the initial phases, when a series of stress reactions and immune responses are initiated. Peripheral CD4&lt;sup>+&lt;/sup> T cells have been reported as the major contributors to the occurrence of mental disorders. Chronic stress exposure-evoked release of cytokines can promote the differentiation of peripheral CD4&lt;sup>+&lt;/sup> cells into various phenotypes. Among them, Th17 cells have attracted much attention due to their high pathogen</pubmed_abstract><journal>Journal of neuroinflammation</journal><pubmed_title>Chronic stress-induced depression requires the recruitment of peripheral Th17 cells into the brain.</pubmed_title><pmcid>PMC9281140</pmcid><funding_grant_id>19B422</funding_grant_id><funding_grant_id>82171493</funding_grant_id><funding_grant_id>2021JJ30504</funding_grant_id><pubmed_authors>Yuan T</pubmed_authors><pubmed_authors>Zhao B</pubmed_authors><pubmed_authors>Peng S</pubmed_authors><pubmed_authors>Tuo Q</pubmed_authors><pubmed_authors>Liao D</pubmed_authors><pubmed_authors>Lin K</pubmed_authors><pubmed_authors>Shi Z</pubmed_authors><pubmed_authors>Peng Z</pubmed_authors><pubmed_authors>Wei L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chronic stress-induced depression requires the recruitment of peripheral Th17 cells into the brain.</name><description>&lt;h4>Background&lt;/h4>Depression is a recurrent and devastating mental disease that is highly prevalent worldwide. Prolonged exposure to stressful events or a stressful environment is detrimental to mental health. In recent years, an inflammatory hypothesis has been implicated in the pathogenesis of stress-induced depression. However, less attention has been given to the initial phases, when a series of stress reactions and immune responses are initiated. Peripheral CD4&lt;sup>+&lt;/sup> T cells have been reported as the major contributors to the occurrence of mental disorders. Chronic stress exposure-evoked release of cytokines can promote the differentiation of peripheral CD4&lt;sup>+&lt;/sup> cells into various phenotypes. Among them, Th17 cells have attracted much attention due to their high pathogen</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-22T06:07:49.755Z</modification><creation>2022-07-19T08:13:11.404Z</creation></dates><accession>S-EPMC9281140</accession><cross_references><pubmed>35836182</pubmed><doi>10.1186/s12974-022-02543-6</doi></cross_references></HashMap>