dc.creatorMartinez, Fernando O.
dc.creatorCombes, Theo W.
dc.creatorOrsenigo, Federica
dc.creatorGordon, Siamon
dc.date.accessioned2020-09-04T16:20:42Z
dc.date.accessioned2022-09-23T18:57:05Z
dc.date.available2020-09-04T16:20:42Z
dc.date.available2022-09-23T18:57:05Z
dc.date.created2020-09-04T16:20:42Z
dc.identifier2352-3964
dc.identifierhttps://doi.org/10.1016/j.ebiom.2020.102964
dc.identifierhttp://hdl.handle.net/20.500.12010/12707
dc.identifierhttps://doi.org/10.1016/j.ebiom.2020.102964
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3510228
dc.description.abstractMononuclear phagocytes are a widely distributed family of cells contributing to innate and adaptive immunity. Circulating monocytes and tissue macrophages participate in all stages of SARS COVID-19. They contribute to comorbidities predisposing to clinical infection, virus resistance and dissemination, and to host factors that determine disease severity, recovery and sequelae. Assays are available to detect viral infection and antibody responses, but no adequate tests have been developed to measure the activation level of monocytes and tissue macrophages, and the risk of progression to a fatal hyperinflammatory syndrome. Blood monocytes provide a window on the systemic immune response, from production to tissue recruitment, reflecting the impact of infection on the host. Ready availability of blood makes it possible to monitor severity and the risk of potentially lethal complications, by developing tests to assess the status of monocyte activation and its potential for further inflammatory dysregulation after recruitment to tissues and during recovery.
dc.languageeng
dc.publisherEBioMedicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAbierto (Texto Completo)
dc.sourcereponame:Expeditio Repositorio Institucional UJTL
dc.sourceinstname:Universidad de Bogotá Jorge Tadeo Lozano
dc.subjectCsf1r
dc.subjectCsf2r
dc.subjectCsf3r
dc.subjectMonocyte
dc.subjectActivation
dc.subjectMacrophages
dc.subjectCOVID-19
dc.titleMonocyte activation in systemic Covid-19 infection: Assay and rationale


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