<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Song E</submitter><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pubmed_abstract>One third of COVID-19 patients develop significant neurological symptoms, yet SARS-CoV-2 is rarely detected in central nervous system (CNS) tissue, suggesting a potential role for parainfectious processes, including neuroimmune responses. We therefore examined immune parameters in cerebrospinal fluid (CSF) and blood samples from a cohort of patients with COVID-19 and significant neurological complications. We found divergent immunological responses in the CNS compartment, including increased levels of IL-12 and IL-12-associated innate and adaptive immune cell activation. Moreover, we found increased proportions of B cells in the CSF relative to the periphery and evidence of clonal expansion of CSF B cells, suggesting a divergent intrathecal humoral response to SARS-CoV-2. Indeed, all COVID</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2020.09.11.293464</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7491516</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exploratory neuroimmune profiling identifies CNS-specific alterations in COVID-19 patients with neurological involvement.</pubmed_title><pmcid>PMC7491516</pmcid><funding_grant_id>R01 MH122471</funding_grant_id><funding_grant_id>F30 CA239444</funding_grant_id><funding_grant_id>F30 CA250249</funding_grant_id><funding_grant_id>T32 GM136651</funding_grant_id><funding_grant_id>U19 AI089992</funding_grant_id><funding_grant_id>K23 MH118999</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>S10 OD021801</funding_grant_id><funding_grant_id>R01 AI157488</funding_grant_id><funding_grant_id>K08 NS096117</funding_grant_id><funding_grant_id>R21 MH118109</funding_grant_id><funding_grant_id>R01 AI104739</funding_grant_id><pubmed_authors>Gallego JA</pubmed_authors><pubmed_authors>Bartley CM</pubmed_authors><pubmed_authors>Alvarenga BD</pubmed_authors><pubmed_authors>Mao T</pubmed_authors><pubmed_authors>Oh J</pubmed_authors><pubmed_authors>Pleasure SJ</pubmed_authors><pubmed_authors>Zamecnik CR</pubmed_authors><pubmed_authors>Chow RD</pubmed_authors><pubmed_authors>Jiang R</pubmed_authors><pubmed_authors>Phinney BS</pubmed_authors><pubmed_authors>Rahman NT</pubmed_authors><pubmed_authors>Alexander J</pubmed_authors><pubmed_authors>Dai Y</pubmed_authors><pubmed_authors>Lucas C</pubmed_authors><pubmed_authors>Lencz T</pubmed_authors><pubmed_authors>Ngo TT</pubmed_authors><pubmed_authors>Iwasaki A</pubmed_authors><pubmed_authors>Vogels CBF</pubmed_authors><pubmed_authors>Grubaugh ND</pubmed_authors><pubmed_authors>Walsh H</pubmed_authors><pubmed_authors>Casanovas-Massana A</pubmed_authors><pubmed_authors>Kleinstein SH</pubmed_authors><pubmed_authors>Dandekar R</pubmed_authors><pubmed_authors>Goldman-Israelow B</pubmed_authors><pubmed_authors>Ko AI</pubmed_authors><pubmed_authors>Ring A</pubmed_authors><pubmed_authors>Loudermilk RP</pubmed_authors><pubmed_authors>Huynh T</pubmed_authors><pubmed_authors>DeRisi JL</pubmed_authors><pubmed_authors>Farhadian SF</pubmed_authors><pubmed_authors>Chiarella J</pubmed_authors><pubmed_authors>Wilson MR</pubmed_authors><pubmed_authors>McAlpine L</pubmed_authors><pubmed_authors>Hawes IA</pubmed_authors><pubmed_authors>Song E</pubmed_authors><pubmed_authors>Klein J</pubmed_authors><pubmed_authors>Spudich S</pubmed_authors><pubmed_authors>Geng B</pubmed_authors><pubmed_authors>Salemi M</pubmed_authors><pubmed_authors>Liu F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exploratory neuroimmune profiling identifies CNS-specific alterations in COVID-19 patients with neurological involvement.</name><description>One third of COVID-19 patients develop significant neurological symptoms, yet SARS-CoV-2 is rarely detected in central nervous system (CNS) tissue, suggesting a potential role for parainfectious processes, including neuroimmune responses. We therefore examined immune parameters in cerebrospinal fluid (CSF) and blood samples from a cohort of patients with COVID-19 and significant neurological complications. We found divergent immunological responses in the CNS compartment, including increased levels of IL-12 and IL-12-associated innate and adaptive immune cell activation. Moreover, we found increased proportions of B cells in the CSF relative to the periphery and evidence of clonal expansion of CSF B cells, suggesting a divergent intrathecal humoral response to SARS-CoV-2. Indeed, all COVID</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2026-05-03T03:25:03.47Z</modification><creation>2020-09-20T07:02:21Z</creation></dates><accession>S-EPMC7491516</accession><cross_references><pubmed>32935102</pubmed><doi>10.1101/2020.09.11.293464</doi></cross_references></HashMap>