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Campo DC | Valor | Lengua/Idioma |
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dc.contributor.author | Acosta Ampudia, Yeny | - |
dc.contributor.author | Monsalve, Diana M. | - |
dc.contributor.author | Rojas, Manuel | - |
dc.contributor.author | Rodríguez, Yhojan | - |
dc.contributor.author | Gallo Bonilla, Juan Esteban | - |
dc.contributor.author | Salazar Uribe, Juan Carlos | - |
dc.contributor.author | Santander, María José | - |
dc.contributor.author | Cala, Mónica P. | - |
dc.contributor.author | Zapata Builes, Wildeman | - |
dc.contributor.author | Zapata Cardona, María Isabel | - |
dc.contributor.author | Manrique, Rubén | - |
dc.contributor.author | Pardo Oviedo, Juan Mauricio | - |
dc.contributor.author | Camacho, Bernardo | - |
dc.contributor.author | Ramírez Santana, Carolina | - |
dc.contributor.author | Anaya Cabrera, Juan Manuel | - |
dc.date.accessioned | 2022-05-17T21:35:38Z | - |
dc.date.available | 2022-05-17T21:35:38Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Anaya 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, 2021 | spa |
dc.identifier.issn | 0896-8411 | - |
dc.identifier.uri | http://hdl.handle.net/10495/28424 | - |
dc.description.abstract | ABSTRACT: 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.extent | 16 | spa |
dc.format.mimetype | application/pdf | spa |
dc.language.iso | eng | spa |
dc.publisher | Academic Press | spa |
dc.type.hasversion | info:eu-repo/semantics/publishedVersion | spa |
dc.rights | info:eu-repo/semantics/openAccess | spa |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/2.5/co/ | * |
dc.title | COVID-19 convalescent plasma composition and immunological effects in severe patients | spa |
dc.type | info:eu-repo/semantics/article | spa |
dc.publisher.group | Inmunovirología | spa |
dc.identifier.doi | 10.1016/j.jaut.2021.102598 | - |
oaire.version | http://purl.org/coar/version/c_970fb48d4fbd8a85 | spa |
dc.rights.accessrights | http://purl.org/coar/access_right/c_abf2 | spa |
dc.identifier.eissn | 1095-9157 | - |
oaire.citationtitle | Journal of Autoimmunity | spa |
oaire.citationstartpage | 1 | spa |
oaire.citationendpage | 16 | spa |
oaire.citationvolume | 118 | spa |
dc.rights.creativecommons | https://creativecommons.org/licenses/by-nc-nd/4.0/ | spa |
dc.publisher.place | Londres, Inglaterra | spa |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | spa |
dc.type.redcol | https://purl.org/redcol/resource_type/ART | spa |
dc.type.local | Artículo de investigación | spa |
dc.subject.decs | COVID-19 | - |
dc.subject.decs | Cytokines | - |
dc.subject.decs | Citocinas | - |
dc.subject.decs | Autoantibodies | - |
dc.subject.decs | Autoanticuerpos | - |
dc.subject.decs | Immunization, Passive | - |
dc.subject.decs | Inmunización Pasiva | - |
dc.description.researchgroupid | 0012444 | spa |
dc.description.researchgroupid | COL0012444 | spa |
dc.relation.ispartofjournalabbrev | J Autoimmun | spa |
Aparece en las colecciones: | Artículos de Revista en Ciencias Médicas |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
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ZapataWildeman_2021_COVID19ConvalescentPlasma.pdf | Artículo de investigación | 3.87 MB | Adobe PDF | Visualizar/Abrir |
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