Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.

Seija, Mariana - Rammauro, Florencia

Resumen:

Background. Antibody response against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) after mRNA or adenoviral vector-based vaccines is weak in kidney transplant (KT) patients. However, few studies have focused on humoral response after inactivated virus-based vaccines in KT. Here, we compare antibody response following vaccination with inactivated virus (CoronaVac®) and BNT162b2 mRNA. Methods. A national multicentre cross-sectional study was conducted. The study group was composed of patients from all KT centres in Uruguay, vaccinated between 1 and 31 May 2021 (CoronaVac®, n = 245 and BNT162b2, n = 39). The control group was constituted of 82 healthy individuals. Participants had no prior confirmed coronavirus disease 2019 (COVID-19) test. Blood samples were collected between 30 and 40 days after the second dose. Serum-specific immunoglobulin G (IgG) antibodies against the receptor-binding domain (RBD) of SARS-CoV-2 Spike protein were determined using the COVID-19 IgG QUANT ELISA Kit. Results. Only 29% of KT recipients showed seroconversion (36.5% BNT162b2, 27.8% inactivated virus, P = 0.248) in comparison with 100% in healthy control with either vaccine. Antibody levels against RBD were higher with BNT162b mRNA than with inactivated virus [median (interquartile range) 173 (73–554) and 29 (11–70) binding antibody units (BAU)/mL, P < 0.034] in KT and 10 times lower than healthy control [inactivated virus: 308 (209–335) and BNT162b2: 2638 (2608–3808) BAU/mL, P < 0.034]. In multivariate analysis, variables associated with negative humoral response were age, triple immunosuppression, estimated glomerular filtration rate and time post-KT. Conclusion. Seroconversion was low in KT patients after vaccination with both platforms. Antibody levels against SARS-CoV-2 were lower with inactivated virus than BNT162b mRNA. These findings support the need for strategies to improve immunogenicity in KT recipients after two doses of either vaccine.


Detalles Bibliográficos
2022
Fondo para la Convergencia Estructural del Mercosur (FOCEM, COF 03/11); Agencia Nacional de Investigación e Innovación (ANII), Uruguay; y Fondo de Investigación en Nefrología (FOINE), Hospital de Clínicas, Uruguay.
COVID-19
Kidney transplantation
SARS-CoV-2 vaccine
KIDNEY
RIÑONES
ANTIBODY RESPONSE
FORMACIÓN DE ANTICUERPOS
TRASPLANTE DE RIÑÓN
Inglés
Universidad de la República
COLIBRI
https://hdl.handle.net/20.500.12008/40556
https://doi.org/10.1093/ckj/sfab291
Acceso abierto
Licencia Creative Commons Atribución - No Comercial - Sin Derivadas (CC - By-NC-ND 4.0)
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author2 Rammauro, Florencia
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author_facet Seija, Mariana
Rammauro, Florencia
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dc.contributor.filiacion.none.fl_str_mv Seija Mariana, Universidad de la República (Uruguay). Facultad de Medicina
Rammauro Florencia, Universidad de la República (Uruguay). Facultad de Medicina
dc.creator.none.fl_str_mv Seija, Mariana
Rammauro, Florencia
dc.date.accessioned.none.fl_str_mv 2023-10-06T13:45:07Z
dc.date.available.none.fl_str_mv 2023-10-06T13:45:07Z
dc.date.issued.none.fl_str_mv 2022
dc.description.abstract.none.fl_txt_mv Background. Antibody response against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) after mRNA or adenoviral vector-based vaccines is weak in kidney transplant (KT) patients. However, few studies have focused on humoral response after inactivated virus-based vaccines in KT. Here, we compare antibody response following vaccination with inactivated virus (CoronaVac®) and BNT162b2 mRNA. Methods. A national multicentre cross-sectional study was conducted. The study group was composed of patients from all KT centres in Uruguay, vaccinated between 1 and 31 May 2021 (CoronaVac®, n = 245 and BNT162b2, n = 39). The control group was constituted of 82 healthy individuals. Participants had no prior confirmed coronavirus disease 2019 (COVID-19) test. Blood samples were collected between 30 and 40 days after the second dose. Serum-specific immunoglobulin G (IgG) antibodies against the receptor-binding domain (RBD) of SARS-CoV-2 Spike protein were determined using the COVID-19 IgG QUANT ELISA Kit. Results. Only 29% of KT recipients showed seroconversion (36.5% BNT162b2, 27.8% inactivated virus, P = 0.248) in comparison with 100% in healthy control with either vaccine. Antibody levels against RBD were higher with BNT162b mRNA than with inactivated virus [median (interquartile range) 173 (73–554) and 29 (11–70) binding antibody units (BAU)/mL, P < 0.034] in KT and 10 times lower than healthy control [inactivated virus: 308 (209–335) and BNT162b2: 2638 (2608–3808) BAU/mL, P < 0.034]. In multivariate analysis, variables associated with negative humoral response were age, triple immunosuppression, estimated glomerular filtration rate and time post-KT. Conclusion. Seroconversion was low in KT patients after vaccination with both platforms. Antibody levels against SARS-CoV-2 were lower with inactivated virus than BNT162b mRNA. These findings support the need for strategies to improve immunogenicity in KT recipients after two doses of either vaccine.
dc.description.es.fl_txt_mv Todos los Autores y su Filiación: Mariana Seija 1,2, Florencia Rammauro3,4, José Santiago1, Natalia Orihuela5, Catherine Zulberti5, Danilo Machado6, Cecilia Recalde6, Javier Noboa1,4, Victoria Frantchez7, Rossana Astesiano1, Federico Yandián1, Ana Guerisoli1, Álvaro Morra5, Daniela Cassinelli8, Cecilia Coelho8, Belén de Aramburu8, Paulina González-Severgnini8, Romina Moreno8, Aldana Pippolo8, Gabriela López9, Mónica Lemos9, Lorena Somariva9, Eliana López9, Soledad Fumero9, Carla Orihuela9, Rosalía Rodríguez6, Gonzalo Acuña6, Victoria Rabaza6, Nancy Perg6, Rossana Cordero6, Cristina Reisfeld6, Paula Olivera6, Paola Montero6, Cecilia Nogueira6, Catheryn Nalerio5, Sergio Orihuela5, Lilián Curi5, Ema Burgstaller6, Oscar Noboa1, Otto Pritsch3,4, Marcelo Nin1,5 and Sergio Bianchi 2,10 1Centro de Nefrología, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 2Departamento de Fisiopatología, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 3Laboratorio de Inmunovirología, Institut Pasteur de Montevideo, Montevideo, Uruguay, 4Departamento de Inmunobiología, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 5Centro de Trasplante INU, Hospital Italiano, Montevideo, Uruguay, 6Centro de Trasplante, Hospital Evangélico, Montevideo, Uruguay, 7Cátedra de Enfermedades Infecciosas, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 8Students of Scientific Methods 2, Medical Doctor Degree, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 9Departamento de Enfermería, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay and 10Laboratorio de Genómica Funcional, Institut Pasteur de Montevideo, Montevideo, Uruguay ∗These authors contributed equally to this work. Correspondence to: Sergio Bianchi; E-mail: sbianchi@fmed.edu.uy
dc.description.sponsorship.none.fl_txt_mv Fondo para la Convergencia Estructural del Mercosur (FOCEM, COF 03/11); Agencia Nacional de Investigación e Innovación (ANII), Uruguay; y Fondo de Investigación en Nefrología (FOINE), Hospital de Clínicas, Uruguay.
dc.format.extent.es.fl_str_mv 7 p.
dc.format.mimetype.es.fl_str_mv application/pdf
dc.identifier.citation.es.fl_str_mv Seija M, Rammauro F y otros. Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant. Clinical Kidney Journal [en línea] 2022; 15(3): 527–533. 7 p.
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1093/ckj/sfab291
dc.identifier.issn.none.fl_str_mv 2048-8505
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12008/40556
dc.language.iso.none.fl_str_mv en
eng
dc.publisher.es.fl_str_mv Oxford University Press on behalf of the ERA [European Renal Association]
dc.relation.ispartof.es.fl_str_mv Clinical Kidney Journal, 2022; 15(3): 527–533
dc.rights.license.none.fl_str_mv Licencia Creative Commons Atribución - No Comercial - Sin Derivadas (CC - By-NC-ND 4.0)
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:COLIBRI
instname:Universidad de la República
instacron:Universidad de la República
dc.subject.es.fl_str_mv COVID-19
Kidney transplantation
SARS-CoV-2 vaccine
dc.subject.other.es.fl_str_mv KIDNEY
RIÑONES
ANTIBODY RESPONSE
FORMACIÓN DE ANTICUERPOS
TRASPLANTE DE RIÑÓN
dc.title.none.fl_str_mv Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.
dc.type.es.fl_str_mv Artículo
dc.type.none.fl_str_mv info:eu-repo/semantics/article
dc.type.version.none.fl_str_mv info:eu-repo/semantics/publishedVersion
description Todos los Autores y su Filiación: Mariana Seija 1,2, Florencia Rammauro3,4, José Santiago1, Natalia Orihuela5, Catherine Zulberti5, Danilo Machado6, Cecilia Recalde6, Javier Noboa1,4, Victoria Frantchez7, Rossana Astesiano1, Federico Yandián1, Ana Guerisoli1, Álvaro Morra5, Daniela Cassinelli8, Cecilia Coelho8, Belén de Aramburu8, Paulina González-Severgnini8, Romina Moreno8, Aldana Pippolo8, Gabriela López9, Mónica Lemos9, Lorena Somariva9, Eliana López9, Soledad Fumero9, Carla Orihuela9, Rosalía Rodríguez6, Gonzalo Acuña6, Victoria Rabaza6, Nancy Perg6, Rossana Cordero6, Cristina Reisfeld6, Paula Olivera6, Paola Montero6, Cecilia Nogueira6, Catheryn Nalerio5, Sergio Orihuela5, Lilián Curi5, Ema Burgstaller6, Oscar Noboa1, Otto Pritsch3,4, Marcelo Nin1,5 and Sergio Bianchi 2,10 1Centro de Nefrología, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 2Departamento de Fisiopatología, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 3Laboratorio de Inmunovirología, Institut Pasteur de Montevideo, Montevideo, Uruguay, 4Departamento de Inmunobiología, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 5Centro de Trasplante INU, Hospital Italiano, Montevideo, Uruguay, 6Centro de Trasplante, Hospital Evangélico, Montevideo, Uruguay, 7Cátedra de Enfermedades Infecciosas, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 8Students of Scientific Methods 2, Medical Doctor Degree, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 9Departamento de Enfermería, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay and 10Laboratorio de Genómica Funcional, Institut Pasteur de Montevideo, Montevideo, Uruguay ∗These authors contributed equally to this work. Correspondence to: Sergio Bianchi; E-mail: sbianchi@fmed.edu.uy
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rights_invalid_str_mv Licencia Creative Commons Atribución - No Comercial - Sin Derivadas (CC - By-NC-ND 4.0)
spelling Seija Mariana, Universidad de la República (Uruguay). Facultad de MedicinaRammauro Florencia, Universidad de la República (Uruguay). Facultad de Medicina2023-10-06T13:45:07Z2023-10-06T13:45:07Z2022Seija M, Rammauro F y otros. Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant. Clinical Kidney Journal [en línea] 2022; 15(3): 527–533. 7 p.2048-8505https://hdl.handle.net/20.500.12008/40556https://doi.org/10.1093/ckj/sfab291Todos los Autores y su Filiación: Mariana Seija 1,2, Florencia Rammauro3,4, José Santiago1, Natalia Orihuela5, Catherine Zulberti5, Danilo Machado6, Cecilia Recalde6, Javier Noboa1,4, Victoria Frantchez7, Rossana Astesiano1, Federico Yandián1, Ana Guerisoli1, Álvaro Morra5, Daniela Cassinelli8, Cecilia Coelho8, Belén de Aramburu8, Paulina González-Severgnini8, Romina Moreno8, Aldana Pippolo8, Gabriela López9, Mónica Lemos9, Lorena Somariva9, Eliana López9, Soledad Fumero9, Carla Orihuela9, Rosalía Rodríguez6, Gonzalo Acuña6, Victoria Rabaza6, Nancy Perg6, Rossana Cordero6, Cristina Reisfeld6, Paula Olivera6, Paola Montero6, Cecilia Nogueira6, Catheryn Nalerio5, Sergio Orihuela5, Lilián Curi5, Ema Burgstaller6, Oscar Noboa1, Otto Pritsch3,4, Marcelo Nin1,5 and Sergio Bianchi 2,10 1Centro de Nefrología, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 2Departamento de Fisiopatología, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 3Laboratorio de Inmunovirología, Institut Pasteur de Montevideo, Montevideo, Uruguay, 4Departamento de Inmunobiología, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 5Centro de Trasplante INU, Hospital Italiano, Montevideo, Uruguay, 6Centro de Trasplante, Hospital Evangélico, Montevideo, Uruguay, 7Cátedra de Enfermedades Infecciosas, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 8Students of Scientific Methods 2, Medical Doctor Degree, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay, 9Departamento de Enfermería, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay and 10Laboratorio de Genómica Funcional, Institut Pasteur de Montevideo, Montevideo, Uruguay ∗These authors contributed equally to this work. Correspondence to: Sergio Bianchi; E-mail: sbianchi@fmed.edu.uyBackground. Antibody response against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) after mRNA or adenoviral vector-based vaccines is weak in kidney transplant (KT) patients. However, few studies have focused on humoral response after inactivated virus-based vaccines in KT. Here, we compare antibody response following vaccination with inactivated virus (CoronaVac®) and BNT162b2 mRNA. Methods. A national multicentre cross-sectional study was conducted. The study group was composed of patients from all KT centres in Uruguay, vaccinated between 1 and 31 May 2021 (CoronaVac®, n = 245 and BNT162b2, n = 39). The control group was constituted of 82 healthy individuals. Participants had no prior confirmed coronavirus disease 2019 (COVID-19) test. Blood samples were collected between 30 and 40 days after the second dose. Serum-specific immunoglobulin G (IgG) antibodies against the receptor-binding domain (RBD) of SARS-CoV-2 Spike protein were determined using the COVID-19 IgG QUANT ELISA Kit. Results. Only 29% of KT recipients showed seroconversion (36.5% BNT162b2, 27.8% inactivated virus, P = 0.248) in comparison with 100% in healthy control with either vaccine. Antibody levels against RBD were higher with BNT162b mRNA than with inactivated virus [median (interquartile range) 173 (73–554) and 29 (11–70) binding antibody units (BAU)/mL, P < 0.034] in KT and 10 times lower than healthy control [inactivated virus: 308 (209–335) and BNT162b2: 2638 (2608–3808) BAU/mL, P < 0.034]. In multivariate analysis, variables associated with negative humoral response were age, triple immunosuppression, estimated glomerular filtration rate and time post-KT. Conclusion. Seroconversion was low in KT patients after vaccination with both platforms. Antibody levels against SARS-CoV-2 were lower with inactivated virus than BNT162b mRNA. These findings support the need for strategies to improve immunogenicity in KT recipients after two doses of either vaccine.Submitted by Cicero Alessandra (alesscicero@gmail.com) on 2023-10-05T18:00:10Z No. of bitstreams: 2 license_rdf: 25790 bytes, checksum: 489f03e71d39068f329bdec8798bce58 (MD5) Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant .pdf: 969248 bytes, checksum: 2b80b1ccda151006211b73df71f9f1f7 (MD5)Approved for entry into archive by Almiñana María Cecilia (marialminana@gmail.com) on 2023-10-06T13:29:30Z (GMT) No. of bitstreams: 2 license_rdf: 25790 bytes, checksum: 489f03e71d39068f329bdec8798bce58 (MD5) Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant .pdf: 969248 bytes, checksum: 2b80b1ccda151006211b73df71f9f1f7 (MD5)Made available in DSpace by Luna Fabiana (fabiana.luna@seciu.edu.uy) on 2023-10-06T13:45:07Z (GMT). No. of bitstreams: 2 license_rdf: 25790 bytes, checksum: 489f03e71d39068f329bdec8798bce58 (MD5) Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant .pdf: 969248 bytes, checksum: 2b80b1ccda151006211b73df71f9f1f7 (MD5) Previous issue date: 2022Fondo para la Convergencia Estructural del Mercosur (FOCEM, COF 03/11); Agencia Nacional de Investigación e Innovación (ANII), Uruguay; y Fondo de Investigación en Nefrología (FOINE), Hospital de Clínicas, Uruguay.7 p.application/pdfenengOxford University Press on behalf of the ERA [European Renal Association]Clinical Kidney Journal, 2022; 15(3): 527–533Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)info:eu-repo/semantics/openAccessLicencia Creative Commons Atribución - No Comercial - Sin Derivadas (CC - By-NC-ND 4.0)COVID-19Kidney transplantationSARS-CoV-2 vaccineKIDNEYRIÑONESANTIBODY RESPONSEFORMACIÓN DE ANTICUERPOSTRASPLANTE DE RIÑÓNComparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.Artículoinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:COLIBRIinstname:Universidad de la Repúblicainstacron:Universidad de la RepúblicaSeija, MarianaRammauro, FlorenciaLICENSElicense.txtlicense.txttext/plain; charset=utf-84267http://localhost:8080/xmlui/bitstream/20.500.12008/40556/5/license.txt6429389a7df7277b72b7924fdc7d47a9MD55CC-LICENSElicense_urllicense_urltext/plain; charset=utf-850http://localhost:8080/xmlui/bitstream/20.500.12008/40556/2/license_urla006180e3f5b2ad0b88185d14284c0e0MD52license_textlicense_texttext/html; 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- Universidad de la Repúblicafalse
spellingShingle Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.
Seija, Mariana
COVID-19
Kidney transplantation
SARS-CoV-2 vaccine
KIDNEY
RIÑONES
ANTIBODY RESPONSE
FORMACIÓN DE ANTICUERPOS
TRASPLANTE DE RIÑÓN
status_str publishedVersion
title Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.
title_full Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.
title_fullStr Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.
title_full_unstemmed Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.
title_short Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.
title_sort Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant.
topic COVID-19
Kidney transplantation
SARS-CoV-2 vaccine
KIDNEY
RIÑONES
ANTIBODY RESPONSE
FORMACIÓN DE ANTICUERPOS
TRASPLANTE DE RIÑÓN
url https://hdl.handle.net/20.500.12008/40556
https://doi.org/10.1093/ckj/sfab291