<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Foo SS</submitter><funding>NIDCR NIH HHS</funding><funding>NICHD NIH HHS</funding><funding>Simons Foundation Autism Research Initiative</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>Medical Research Council</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><pagination>100453</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8549189</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2(11)</volume><pubmed_abstract>While pregnancy increases the risk for severe COVID-19, the clinical and immunological implications of COVID-19 on maternal-fetal health remain unknown. Here, we present the clinical and immunological landscapes of 93 COVID-19 mothers and 45 of their SARS-CoV-2-exposed infants through comprehensive serum proteomics profiling for >1,400 cytokines of their peripheral and cord blood specimens. Prenatal SARS-CoV-2 infection triggers NF-κB-dependent proinflammatory immune activation. Pregnant women with severe COVID-19 show increased inflammation and unique IFN-λ antiviral signaling, with elevated levels of IFNL1 and IFNLR1. Furthermore, SARS-CoV-2 infection re-shapes maternal immunity at delivery, altering the expression of pregnancy complication-associated cytokines, inducing MMP7, MDK, and E</pubmed_abstract><journal>Cell reports. Medicine</journal><pubmed_title>The systemic inflammatory landscape of COVID-19 in pregnancy: Extensive serum proteomic profiling of mother-infant dyads with &amp;lt;i&amp;gt;in utero&amp;lt;/i&amp;gt; SARS-CoV-2.</pubmed_title><pmcid>PMC8549189</pmcid><funding_grant_id>R35 CA200422</funding_grant_id><funding_grant_id>R01 DE028521</funding_grant_id><funding_grant_id>R01 HD089714</funding_grant_id><funding_grant_id>R01 HL060917</funding_grant_id><funding_grant_id>R01 AI140705</funding_grant_id><funding_grant_id>R01 AI140718</funding_grant_id><funding_grant_id>R21 AI129534</funding_grant_id><funding_grant_id>R01 CA251275</funding_grant_id><funding_grant_id>K99 DE028573</funding_grant_id><funding_grant_id>R00 DE028573</funding_grant_id><funding_grant_id>R01 AI152190</funding_grant_id><funding_grant_id>T32 MH080634</funding_grant_id><funding_grant_id>MR/V033530/1</funding_grant_id><funding_grant_id>R21 DE027888</funding_grant_id><funding_grant_id>R01 DE023926</funding_grant_id><pubmed_authors>Janzen C</pubmed_authors><pubmed_authors>Vasconcelos Z</pubmed_authors><pubmed_authors>Nielsen-Saines K</pubmed_authors><pubmed_authors>Rao R</pubmed_authors><pubmed_authors>Soni PR</pubmed_authors><pubmed_authors>Shin WJ</pubmed_authors><pubmed_authors>Cambou MC</pubmed_authors><pubmed_authors>Kerin T</pubmed_authors><pubmed_authors>Contreras D</pubmed_authors><pubmed_authors>Erzurum SC</pubmed_authors><pubmed_authors>Foo SS</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Comhair SAA</pubmed_authors><pubmed_authors>Choi Y</pubmed_authors><pubmed_authors>Cortado R</pubmed_authors><pubmed_authors>Aldrovandi G</pubmed_authors><pubmed_authors>Wu X</pubmed_authors><pubmed_authors>Devaskar S</pubmed_authors><pubmed_authors>Gibson LC</pubmed_authors><pubmed_authors>Cranston J</pubmed_authors><pubmed_authors>Garner O</pubmed_authors><pubmed_authors>Arumugaswami V</pubmed_authors><pubmed_authors>Fuller T</pubmed_authors><pubmed_authors>Asilnejad B</pubmed_authors><pubmed_authors>Brasil P</pubmed_authors><pubmed_authors>Moreira ME</pubmed_authors><pubmed_authors>Mok T</pubmed_authors><pubmed_authors>Jung KL</pubmed_authors><pubmed_authors>Xia T</pubmed_authors><pubmed_authors>Tobin N</pubmed_authors><pubmed_authors>Ghosh S</pubmed_authors><pubmed_authors>Fajardo VM</pubmed_authors><pubmed_authors>Bryson Y</pubmed_authors><pubmed_authors>Ibarrondo FJ</pubmed_authors><pubmed_authors>Jung JU</pubmed_authors><pubmed_authors>Mei J</pubmed_authors><pubmed_authors>Bhattacharya D</pubmed_authors><pubmed_authors>Yang O</pubmed_authors><pubmed_authors>Yang S</pubmed_authors></additional><is_claimable>false</is_claimable><name>The systemic inflammatory landscape of COVID-19 in pregnancy: Extensive serum proteomic profiling of mother-infant dyads with &amp;lt;i&amp;gt;in utero&amp;lt;/i&amp;gt; SARS-CoV-2.</name><description>While pregnancy increases the risk for severe COVID-19, the clinical and immunological implications of COVID-19 on maternal-fetal health remain unknown. Here, we present the clinical and immunological landscapes of 93 COVID-19 mothers and 45 of their SARS-CoV-2-exposed infants through comprehensive serum proteomics profiling for >1,400 cytokines of their peripheral and cord blood specimens. Prenatal SARS-CoV-2 infection triggers NF-κB-dependent proinflammatory immune activation. Pregnant women with severe COVID-19 show increased inflammation and unique IFN-λ antiviral signaling, with elevated levels of IFNL1 and IFNLR1. Furthermore, SARS-CoV-2 infection re-shapes maternal immunity at delivery, altering the expression of pregnancy complication-associated cytokines, inducing MMP7, MDK, and E</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2026-05-08T10:59:51.622Z</modification><creation>2022-02-11T13:13:14.96Z</creation></dates><accession>S-EPMC8549189</accession><cross_references><pubmed>34723226</pubmed><doi>10.1016/j.xcrm.2021.100453</doi></cross_references></HashMap>