<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>96(12)</volume><submitter>Stich M</submitter><funding>The study was funded by the Ministry of Science, Research and the Arts in Baden-Württemberg, Germany, within the framework of the special funding line for COVID-19 research, part of the measures to combat the SARS-CoV-2 pandemic in the field of medical research. Maximilian Stich was funded by the DZIF clinical leave stipend of the German Center for Infection Research.</funding><pubmed_abstract>The pivotal role of the cell entry receptor ACE2 for SARS-CoV-2 infection is well-established. When ACE2 is shed from cell surface into plasma as soluble ACE2 (sACE2), it can effectively neutralize SARS-CoV-2. This longitudinal prospective cohort study analyzed sACE2 activity in 1192 participants, aged 4 months to 81 years, 3 and 12 months after SARS-CoV-2 household exposure. Following SARS-CoV-2 exposure, participants exhibited significantly elevated sACE2 activity, irrespective of confirmed infection, with the highest levels observed in exposed children. Longitudinal analysis revealed a decline in sACE2 levels over time, reaching levels comparable to age- and sex-matched pre-pandemic controls. An increase in sACE2 activity was also confirmed in vitro in Calu-3 (human lung) cells within h</pubmed_abstract><journal>Journal of medical virology</journal><pagination>e70098</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11612704</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Elevated Soluble ACE2 Activity in Children and Adults After SARS-CoV-2 Exposure Irrespective of Laboratory-Confirmed Infection.</pubmed_title><pmcid>PMC11612704</pmcid><pubmed_authors>Jacobsen EM</pubmed_authors><pubmed_authors>Lang P</pubmed_authors><pubmed_authors>Mohr K</pubmed_authors><pubmed_authors>Janda A</pubmed_authors><pubmed_authors>Renk H</pubmed_authors><pubmed_authors>Rabsteyn A</pubmed_authors><pubmed_authors>Bode SFN</pubmed_authors><pubmed_authors>Magalhaes VG</pubmed_authors><pubmed_authors>Krausslich HG</pubmed_authors><pubmed_authors>Okun JG</pubmed_authors><pubmed_authors>Bartenschlager R</pubmed_authors><pubmed_authors>Hoffmann GF</pubmed_authors><pubmed_authors>Burger F</pubmed_authors><pubmed_authors>Garbade SF</pubmed_authors><pubmed_authors>Jeltsch K</pubmed_authors><pubmed_authors>Binder M</pubmed_authors><pubmed_authors>Stich M</pubmed_authors><pubmed_authors>Elling R</pubmed_authors><pubmed_authors>Muller B</pubmed_authors><pubmed_authors>Haddad A</pubmed_authors><pubmed_authors>Tonshoff B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Elevated Soluble ACE2 Activity in Children and Adults After SARS-CoV-2 Exposure Irrespective of Laboratory-Confirmed Infection.</name><description>The pivotal role of the cell entry receptor ACE2 for SARS-CoV-2 infection is well-established. When ACE2 is shed from cell surface into plasma as soluble ACE2 (sACE2), it can effectively neutralize SARS-CoV-2. This longitudinal prospective cohort study analyzed sACE2 activity in 1192 participants, aged 4 months to 81 years, 3 and 12 months after SARS-CoV-2 household exposure. Following SARS-CoV-2 exposure, participants exhibited significantly elevated sACE2 activity, irrespective of confirmed infection, with the highest levels observed in exposed children. Longitudinal analysis revealed a decline in sACE2 levels over time, reaching levels comparable to age- and sex-matched pre-pandemic controls. An increase in sACE2 activity was also confirmed in vitro in Calu-3 (human lung) cells within h</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-04T01:40:15.071Z</modification><creation>2025-04-04T01:40:15.071Z</creation></dates><accession>S-EPMC11612704</accession><cross_references><pubmed>39624009</pubmed><doi>10.1002/jmv.70098</doi></cross_references></HashMap>