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dc.contributor.authorAcosta Ampudia, Yeny-
dc.contributor.authorMonsalve, Diana M.-
dc.contributor.authorRojas, Manuel-
dc.contributor.authorRodríguez, Yhojan-
dc.contributor.authorGallo Bonilla, Juan Esteban-
dc.contributor.authorSalazar Uribe, Juan Carlos-
dc.contributor.authorSantander, María José-
dc.contributor.authorCala, Mónica P.-
dc.contributor.authorZapata Builes, Wildeman-
dc.contributor.authorZapata Cardona, María Isabel-
dc.contributor.authorManrique, Rubén-
dc.contributor.authorPardo Oviedo, Juan Mauricio-
dc.contributor.authorCamacho, Bernardo-
dc.contributor.authorRamírez Santana, Carolina-
dc.contributor.authorAnaya Cabrera, Juan Manuel-
dc.date.accessioned2022-05-17T21:35:38Z-
dc.date.available2022-05-17T21:35:38Z-
dc.date.issued2021-
dc.identifier.citationAnaya JM, Rojas M, Salinas ML., Rodríguez Y, Roa G, Lozano M, Rodríguez Jiménez M, Montoya N, Zapata E, Monsalve DM, Acosta Ampudia Y, Ramírez Santana C. Post-COVID syndrome. A case series and comprehensive review Autoimmunity Reviews, Volume 20, 2021spa
dc.identifier.issn0896-8411-
dc.identifier.urihttp://hdl.handle.net/10495/28424-
dc.description.abstractABSTRACT: Convalescent plasma (CP) has emerged as a treatment for COVID-19. However, the composition and mechanism of action are not fully known. Therefore, we undertook a two-phase controlled study in which, first the immunological and metabolomic status of recovered and severe patients were evaluated. Secondly, the 28-day effect of CP on the immune response in severe patients was assessed. Nineteen recovered COVID-19 patients, 18 hospitalized patients with severe disease, and 16 pre-pandemic controls were included. Patients with severe disease were treated with CP transfusion and standard therapy (i.e., plasma recipients, n = 9) or standard therapy alone (n = 9). Clinical and biological assessments were done on day 0 and during follow-up on days 4, 7, 14, and 28. Clinical parameters, viral load, total immunoglobulin (Ig) G and IgA anti-S1-SARS-CoV-2 antibodies, neutralizing antibodies (NAbs), autoantibodies, cytokines, T and B cells, and metabolomic and lipidomic profiles were examined. Total IgG and IgA anti-S1-SARS-CoV-2 antibodies were key factors for CP selection and correlated with NAbs. In severe COVID-19 patients, mostly interleukin (IL)-6 (P = <0.0001), IL-10 (P = <0.0001), IP-10 (P = <0.0001), fatty acyls and glycerophospholipids were higher than in recovered patients. Latent autoimmunity and anti–IFN–α antibodies were observed in both recovered and severe patients. COVID-19 CP induced an early but transient cytokine profile modification and increases IgG anti-S1-SARS-CoV-2 antibodies. At day 28 post-transfusion, a decrease in activated, effector and effector memory CD4+ (P < 0.05) and activated and effector CD8+ (P < 0.01) T cells and naïve B cells (P = 0.001), and an increase in non-classical memory B cells (P=<0.0001) and central memory CD4+ T cells (P = 0.0252) were observed. Moreover, IL-6/IFN-γ (P = 0.0089) and IL-6/IL-10 (P = 0.0180) ratios decreased in plasma recipients compared to those who received standard therapy alone. These results may have therapeutic implications and justify further post-COVID-19 studies.spa
dc.format.extent16spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherAcademic Pressspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleCOVID-19 convalescent plasma composition and immunological effects in severe patientsspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupInmunovirologíaspa
dc.identifier.doi10.1016/j.jaut.2021.102598-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1095-9157-
oaire.citationtitleJournal of Autoimmunityspa
oaire.citationstartpage1spa
oaire.citationendpage16spa
oaire.citationvolume118spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
dc.publisher.placeLondres, Inglaterraspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsCOVID-19-
dc.subject.decsCytokines-
dc.subject.decsCitocinas-
dc.subject.decsAutoantibodies-
dc.subject.decsAutoanticuerpos-
dc.subject.decsImmunization, Passive-
dc.subject.decsInmunización Pasiva-
dc.description.researchgroupid0012444spa
dc.description.researchgroupidCOL0012444spa
dc.relation.ispartofjournalabbrevJ Autoimmunspa
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