<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jackson S</submitter><funding>British Heart Foundation</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Wellcome Trust</funding><pagination>655-668</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7616636</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>A SARS-CoV-2 controlled human infection model (CHIM) has been successfully established in seronegative individuals using a dose of 1×10&lt;sup>1&lt;/sup> 50% tissue culture infectious dose (TCID&lt;sub>50&lt;/sub>) pre-alpha SARS-CoV-2 virus. Given the increasing prevalence of seropositivity to SARS-CoV-2, a CHIM that could be used for vaccine development will need to induce infection in those with pre-existing immunity. Our aim was to find a dose of pre-alpha SARS-CoV-2 virus that induced infection in previously infected individuals.&lt;h4>Methods&lt;/h4>Healthy, UK volunteers aged 18-30 years, with proven (quantitative RT-PCR or lateral flow antigen test) previous SARS-CoV-2 infection (with or without vaccination) were inoculated intranasally in a stepwise dose escalation CHIM with eith</pubmed_abstract><journal>The Lancet. Microbe</journal><pubmed_title>Safety, tolerability, viral kinetics, and immune correlates of protection in healthy, seropositive UK adults inoculated with SARS-CoV-2: a single-centre, open-label, phase 1 controlled human infection study.</pubmed_title><pmcid>PMC7616636</pmcid><funding_grant_id>MR/X009297/1</funding_grant_id><funding_grant_id>222305/Z/21/Z</funding_grant_id><funding_grant_id>NIHR300791</funding_grant_id><funding_grant_id>CH/16/1/32013</funding_grant_id><funding_grant_id>222305</funding_grant_id><pubmed_authors>Fredsgaard-Jones TPW</pubmed_authors><pubmed_authors>Sodipo V</pubmed_authors><pubmed_authors>Longet S</pubmed_authors><pubmed_authors>Sette A</pubmed_authors><pubmed_authors>Carroll M</pubmed_authors><pubmed_authors>Patel B</pubmed_authors><pubmed_authors>Pollard AJ</pubmed_authors><pubmed_authors>Catchpole A</pubmed_authors><pubmed_authors>Conway O</pubmed_authors><pubmed_authors>Luciw M</pubmed_authors><pubmed_authors>COV-CHIM01 study team</pubmed_authors><pubmed_authors>Harris SA</pubmed_authors><pubmed_authors>Parvelikudy B</pubmed_authors><pubmed_authors>Marshall JL</pubmed_authors><pubmed_authors>Hughes E</pubmed_authors><pubmed_authors>Benamore R</pubmed_authors><pubmed_authors>Alparaque M</pubmed_authors><pubmed_authors>Tipton T</pubmed_authors><pubmed_authors>Voaides A</pubmed_authors><pubmed_authors>Orobiyi-Rieba M</pubmed_authors><pubmed_authors>Platt A</pubmed_authors><pubmed_authors>Laidlaw S</pubmed_authors><pubmed_authors>Mujadidi Y</pubmed_authors><pubmed_authors>Valmores MA</pubmed_authors><pubmed_authors>Morrison H</pubmed_authors><pubmed_authors>Cabrera Puig I</pubmed_authors><pubmed_authors>Breuer J</pubmed_authors><pubmed_authors>Lopez-Ramon R</pubmed_authors><pubmed_authors>Tanner R</pubmed_authors><pubmed_authors>Barnes E</pubmed_authors><pubmed_authors>Gleeson F</pubmed_authors><pubmed_authors>Quaddy J</pubmed_authors><pubmed_authors>Vuddamalay G</pubmed_authors><pubmed_authors>Stone H</pubmed_authors><pubmed_authors>Preston-Jones H</pubmed_authors><pubmed_authors>Byard N</pubmed_authors><pubmed_authors>Turner C</pubmed_authors><pubmed_authors>Crowther C</pubmed_authors><pubmed_authors>Doherty RP</pubmed_authors><pubmed_authors>Rapeport G</pubmed_authors><pubmed_authors>Ferreira VM</pubmed_authors><pubmed_authors>Mawer A</pubmed_authors><pubmed_authors>Nehiweze A</pubmed_authors><pubmed_authors>Nyamunda S</pubmed_authors><pubmed_authors>Ateere A</pubmed_authors><pubmed_authors>Satti I</pubmed_authors><pubmed_authors>Pswarayi D</pubmed_authors><pubmed_authors>Bharti N</pubmed_authors><pubmed_authors>Jackson S</pubmed_authors><pubmed_authors>McShane H</pubmed_authors><pubmed_authors>Mitchell R</pubmed_authors><pubmed_authors>Chiu C</pubmed_authors><pubmed_authors>Srijith P</pubmed_authors><pubmed_authors>Dunachie SJ</pubmed_authors><pubmed_authors>Stylianou E</pubmed_authors><pubmed_authors>Wu MS</pubmed_authors><pubmed_authors>Samuel BE</pubmed_authors><pubmed_authors>Burns A</pubmed_authors><pubmed_authors>Jose J</pubmed_authors><pubmed_authors>Cooper C</pubmed_authors><pubmed_authors>Anid L</pubmed_authors><pubmed_authors>Johnstone T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety, tolerability, viral kinetics, and immune correlates of protection in healthy, seropositive UK adults inoculated with SARS-CoV-2: a single-centre, open-label, phase 1 controlled human infection study.</name><description>&lt;h4>Background&lt;/h4>A SARS-CoV-2 controlled human infection model (CHIM) has been successfully established in seronegative individuals using a dose of 1×10&lt;sup>1&lt;/sup> 50% tissue culture infectious dose (TCID&lt;sub>50&lt;/sub>) pre-alpha SARS-CoV-2 virus. Given the increasing prevalence of seropositivity to SARS-CoV-2, a CHIM that could be used for vaccine development will need to induce infection in those with pre-existing immunity. Our aim was to find a dose of pre-alpha SARS-CoV-2 virus that induced infection in previously infected individuals.&lt;h4>Methods&lt;/h4>Healthy, UK volunteers aged 18-30 years, with proven (quantitative RT-PCR or lateral flow antigen test) previous SARS-CoV-2 infection (with or without vaccination) were inoculated intranasally in a stepwise dose escalation CHIM with eith</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-01T07:33:18.135Z</modification><creation>2025-04-04T23:48:22.669Z</creation></dates><accession>S-EPMC7616636</accession><cross_references><pubmed>38703782</pubmed><doi>10.1016/S2666-5247(24)00025-9</doi></cross_references></HashMap>