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dc.contributor.otherProducción Científica UCH 2022-
dc.contributor.otherUCH. Departamento de Medicina y Cirugía-
dc.creatorPanizo González, Nayara-
dc.creatorAlbert Vicent, Eliseo Alejandro-
dc.creatorGiménez Civera, Elena-
dc.creatorPuchades Montesa, María Jesús-
dc.creatorD'Marco Gascón, Luis Gerardo-
dc.creatorGandía Salmerón, Lorena-
dc.date2022-
dc.date.accessioned2023-05-31T04:03:05Z-
dc.date.available2023-05-31T04:03:05Z-
dc.date.issued2022-08-31-
dc.identifier.citationPanizo, N., Albert, E., Giménez-Civera, E., Puchades, M. J., D'Marco, L., Gandía-Salmerón, L., Giménez, E., Torre, I., Sancho, A., Gavela, E., Gonzalez-Rico, M., Montomoli, M., Perez-Baylach, C. M., Bonilla, B., Solano, C., Alvarado, M. F., Torregrosa, I., Alcaraz, M. J., Górriz, J. L. & Navarro, D. (2022). Dynamics of SARS-CoV-2-Spike-reactive antibody and T-cell responses in chronic kidney disease patients within 3 months after COVID-19 full vaccination. Clinical Kidney Journal, vol. 15, i. 8 (aug.), pp. 1562–1573. DOI: https://doi.org/10.1093/ckj/sfac093-
dc.identifier.issn2048-8505-
dc.identifier.issn2048-8513 (Electrónico)-
dc.identifier.urihttp://hdl.handle.net/10637/14377-
dc.descriptionEste artículo se encuentra disponible en la siguiente URL: https://academic.oup.com/ckj/article/15/8/1562/6565818-
dc.descriptionEn este artículo de investigación también participan: Estela Giménez, Ignacio Torre, Asunción Sancho, Eva Gavela, Miguel Gonzalez-Rico, Marco Montomoli, Carmen Maria Perez-Baylach, Begoña Bonilla, Camila Solano, M. Fernanda Alvarado, Isidro Torregrosa, María Jesús Alcaraz, José Luis Górriz y David Navarro.-
dc.description.abstractBackground. Little is known regarding the dynamics of antibody and T-cell responses in chronic kidney disease (CKD) following coronavirus disease 2019 (COVID-19) vaccination. Methods. Prospective observational cohort study including 144 participants on haemodialysis (HD) (n = 52) or peritoneal dialysis (PD) (n = 14), those undergoing kidney transplantation (KT) (n = 30) or those with advanced CKD (ACKD) not on dialysis and healthy controls (n = 18). Anti-Spike (S) antibody and T-cell responses were assessed at 15 days (15D) and 3 months (3M) after complete vaccination schedule. HD, PD and KT patients received mRNA vaccines (mRNA-123 and BNT162b2). Most ACKD patients received BNT162b2 (n = 23), or Ad26.COV.2.S (4). Most controls received BNT162b2 (n = 12), or Ad26.COV.2.S (n = 5). Results. Anti-S antibodies at 15D and 3M were detectable in 95% (48/50)/98% (49/50) of HD patients, 93% (13/14)/100% of PD patients, 67% (17/26)/75% (21/28) of KT patients and 96% (25/26)/100% (24/24) of ACKD patients. Rates for healthy controls were 81% (13/16)/100% (17/17). Previous severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2-S) infection was documented in four (7.7%) HD patients, two (14.3%) PD patients, two (6.7%) KT patients, one (5.55%) healthy control and in no ACKD patient. Antibody levels decreased at 3M in HD (P = .04), PD (P = .008) and ACKD patients (P = .0009). In KT patients, levels increased (P = .04) between 15D and 3M, although they were low at both time points. T-cell responses were detected in HD patients in 37 (80%) at baseline, 35 (70%) at 15D and 41 (91%) at 3M. In PD patients, T-cell responses appeared in 8 (67%) at baseline, 13 (93%) at 15D and 9 (100%) at 3M. In KT patients, T-cell responses were detected in 12 (41%) at baseline, 22 (84%) at 15D and 25 (96%) at 3M. In ACKD patients, T-cell responses were detected in 13 (46%) at baseline, 20 (80%) at 15D and 17 (89%) at 3M. None of healthy controls showed T-cell response at baseline, 10 (67%) at 15D and 8 (89%) at 3M. Conclusions. Most HD, PD and ACKD patients develop SARS-CoV-2-S antibody responses comparable to that of healthy controls, in contrast to KT recipients. Antibody waning at 3M was faster in HD, PD and ACKD patients. No differences in SARS-CoV-2 T-cell immunity responses were noticed across study groups.-
dc.formatapplication/pdf-
dc.languagees-
dc.language.isoen-
dc.publisherOxford University-
dc.relationEste artículo de investigación está financiado por el Instituto de Salud Carlos III (cofinanciado por el Fondo Europeo de Desarrollo Regional, FEDER/FEDER) en favor de I.T. (contrato Río Hortega, CM20/00090), de E.A. (contrato Juan Rodés, JR20/00011) y de E.G. (contrato Juan Rodés, JR18/00053).-
dc.relation.ispartofClinical Kidney Journal, vol. 15, n. 8 (aug. 2022)-
dc.rightshttp://creativecommons.org/licenses/by-nc/4.0/deed.es-
dc.subjectRiñones - Enfermedades.-
dc.subjectKidneys - Diseases.-
dc.subjectInmunoglobulinas.-
dc.subjectDiálisis.-
dc.subjectEnfermedades crónicas.-
dc.subjectChronic diseases.-
dc.subjectSARS-CoV-2 (Virus)-
dc.subjectImmunoglobulins.-
dc.subjectRiñones - Trasplante.-
dc.subjectKidneys - Transplantation.-
dc.subjectCélulas T.-
dc.subjectT cells.-
dc.subjectDialysis.-
dc.titleDynamics of SARS-CoV-2-spike-reactive antibody and T-cell responses in chronic kidney disease patients within 3 months after COVID-19 full vaccination-
dc.typeArtículo-
dc.identifier.doihttps://doi.org/10.1093/ckj/sfac093-
dc.relation.projectIDCM20/00090-
dc.relation.projectIDJR20/00011-
dc.relation.projectIDJR18/00053-
dc.centroUniversidad Cardenal Herrera-CEU-
Aparece en las colecciones: Dpto. Medicina y Cirugía




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