<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rendeiro AF</submitter><funding>NCATS NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>564-569</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8204801</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>593(7860)</volume><pubmed_abstract>Recent studies have provided insights into the pathology of and immune response to COVID-19&lt;sup>1-8&lt;/sup>. However, a thorough investigation of the interplay between infected cells and the immune system at sites of infection has been lacking. Here we use high-parameter imaging mass cytometry&lt;sup>9&lt;/sup> that targets the expression of 36 proteins to investigate the cellular composition and spatial architecture of acute lung injury in humans (including injuries derived from SARS-CoV-2 infection) at single-cell resolution. These spatially resolved single-cell data unravel the disordered structure of the infected and injured lung, alongside the distribution of extensive immune infiltration. Neutrophil and macrophage infiltration are hallmarks of bacterial pneumonia and COVID-19, respectively. </pubmed_abstract><journal>Nature</journal><pubmed_title>The spatial landscape of lung pathology during COVID-19 progression.</pubmed_title><pmcid>PMC8204801</pmcid><funding_grant_id>R01 AI107301</funding_grant_id><funding_grant_id>R01 DK121072</funding_grant_id><funding_grant_id>UL1 TR002384</funding_grant_id><funding_grant_id>R01 CA234614</funding_grant_id><funding_grant_id>R01 CA194547</funding_grant_id><funding_grant_id>T32 CA203702</funding_grant_id><funding_grant_id>R03 DK117252</funding_grant_id><pubmed_authors>Bram Y</pubmed_authors><pubmed_authors>Reeves J</pubmed_authors><pubmed_authors>Park J</pubmed_authors><pubmed_authors>Elemento O</pubmed_authors><pubmed_authors>Mason CE</pubmed_authors><pubmed_authors>Warren S</pubmed_authors><pubmed_authors>Rendeiro AF</pubmed_authors><pubmed_authors>Salvatore S</pubmed_authors><pubmed_authors>Meydan C</pubmed_authors><pubmed_authors>Kim J</pubmed_authors><pubmed_authors>Borczuk AC</pubmed_authors><pubmed_authors>Hether T</pubmed_authors><pubmed_authors>Swanson EC</pubmed_authors><pubmed_authors>Schwartz RE</pubmed_authors><pubmed_authors>Chandar V</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Ravichandran H</pubmed_authors><pubmed_authors>Foox J</pubmed_authors></additional><is_claimable>false</is_claimable><name>The spatial landscape of lung pathology during COVID-19 progression.</name><description>Recent studies have provided insights into the pathology of and immune response to COVID-19&lt;sup>1-8&lt;/sup>. However, a thorough investigation of the interplay between infected cells and the immune system at sites of infection has been lacking. Here we use high-parameter imaging mass cytometry&lt;sup>9&lt;/sup> that targets the expression of 36 proteins to investigate the cellular composition and spatial architecture of acute lung injury in humans (including injuries derived from SARS-CoV-2 infection) at single-cell resolution. These spatially resolved single-cell data unravel the disordered structure of the infected and injured lung, alongside the distribution of extensive immune infiltration. Neutrophil and macrophage infiltration are hallmarks of bacterial pneumonia and COVID-19, respectively. </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2026-04-08T09:10:33.712Z</modification><creation>2022-02-11T12:22:43.474Z</creation></dates><accession>S-EPMC8204801</accession><cross_references><pubmed>33780969</pubmed><doi>10.1038/s41586-021-03475-6</doi></cross_references></HashMap>