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

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 c...

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Autores principales: Seija, Mariana, Rammauro, Florencia, Santiago, José, Orihuela, Natalia, Zulberti, Catherine, Machado, Danilo, Recalde, Cecilia, Noboa, Javier, Frantchez, Victoria, Astesiano, Rossana, Yandián, Federico, Guerisoli, Ana, Morra, Álvaro, Cassinelli, Daniela, Coelho, Cecilia, de Aramburu, Belén, González-Severgnini, Paulina, Moreno, Romina, Pippolo, Aldana, López, Gabriela, Lemos, Mónica, Somariva, Lorena, López, Eliana, Fumero, Soledad, Orihuela, Carla, Rodríguez, Rosalía, Acuña, Gonzalo, Rabaza, Victoria, Perg, Nancy, Cordero, Rossana, Reisfeld, Cristina, Olivera, Paula, Montero, Paola, Nogueira, Cecilia, Nalerio, Catheryn, Orihuela, Sergio, Curi, Lilián, Burgstaller, Ema, Noboa, Oscar, Pritsch, Otto, Nin, Marcelo, Bianchi, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755301/
https://www.ncbi.nlm.nih.gov/pubmed/35198159
http://dx.doi.org/10.1093/ckj/sfab291
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author Seija, Mariana
Rammauro, Florencia
Santiago, José
Orihuela, Natalia
Zulberti, Catherine
Machado, Danilo
Recalde, Cecilia
Noboa, Javier
Frantchez, Victoria
Astesiano, Rossana
Yandián, Federico
Guerisoli, Ana
Morra, Álvaro
Cassinelli, Daniela
Coelho, Cecilia
de Aramburu, Belén
González-Severgnini, Paulina
Moreno, Romina
Pippolo, Aldana
López, Gabriela
Lemos, Mónica
Somariva, Lorena
López, Eliana
Fumero, Soledad
Orihuela, Carla
Rodríguez, Rosalía
Acuña, Gonzalo
Rabaza, Victoria
Perg, Nancy
Cordero, Rossana
Reisfeld, Cristina
Olivera, Paula
Montero, Paola
Nogueira, Cecilia
Nalerio, Catheryn
Orihuela, Sergio
Curi, Lilián
Burgstaller, Ema
Noboa, Oscar
Pritsch, Otto
Nin, Marcelo
Bianchi, Sergio
author_facet Seija, Mariana
Rammauro, Florencia
Santiago, José
Orihuela, Natalia
Zulberti, Catherine
Machado, Danilo
Recalde, Cecilia
Noboa, Javier
Frantchez, Victoria
Astesiano, Rossana
Yandián, Federico
Guerisoli, Ana
Morra, Álvaro
Cassinelli, Daniela
Coelho, Cecilia
de Aramburu, Belén
González-Severgnini, Paulina
Moreno, Romina
Pippolo, Aldana
López, Gabriela
Lemos, Mónica
Somariva, Lorena
López, Eliana
Fumero, Soledad
Orihuela, Carla
Rodríguez, Rosalía
Acuña, Gonzalo
Rabaza, Victoria
Perg, Nancy
Cordero, Rossana
Reisfeld, Cristina
Olivera, Paula
Montero, Paola
Nogueira, Cecilia
Nalerio, Catheryn
Orihuela, Sergio
Curi, Lilián
Burgstaller, Ema
Noboa, Oscar
Pritsch, Otto
Nin, Marcelo
Bianchi, Sergio
author_sort Seija, Mariana
collection PubMed
description 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.
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spelling pubmed-87553012022-01-13 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 Santiago, José Orihuela, Natalia Zulberti, Catherine Machado, Danilo Recalde, Cecilia Noboa, Javier Frantchez, Victoria Astesiano, Rossana Yandián, Federico Guerisoli, Ana Morra, Álvaro Cassinelli, Daniela Coelho, Cecilia de Aramburu, Belén González-Severgnini, Paulina Moreno, Romina Pippolo, Aldana López, Gabriela Lemos, Mónica Somariva, Lorena López, Eliana Fumero, Soledad Orihuela, Carla Rodríguez, Rosalía Acuña, Gonzalo Rabaza, Victoria Perg, Nancy Cordero, Rossana Reisfeld, Cristina Olivera, Paula Montero, Paola Nogueira, Cecilia Nalerio, Catheryn Orihuela, Sergio Curi, Lilián Burgstaller, Ema Noboa, Oscar Pritsch, Otto Nin, Marcelo Bianchi, Sergio Clin Kidney J Original Article 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. Oxford University Press 2021-12-27 /pmc/articles/PMC8755301/ /pubmed/35198159 http://dx.doi.org/10.1093/ckj/sfab291 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the ERA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Seija, Mariana
Rammauro, Florencia
Santiago, José
Orihuela, Natalia
Zulberti, Catherine
Machado, Danilo
Recalde, Cecilia
Noboa, Javier
Frantchez, Victoria
Astesiano, Rossana
Yandián, Federico
Guerisoli, Ana
Morra, Álvaro
Cassinelli, Daniela
Coelho, Cecilia
de Aramburu, Belén
González-Severgnini, Paulina
Moreno, Romina
Pippolo, Aldana
López, Gabriela
Lemos, Mónica
Somariva, Lorena
López, Eliana
Fumero, Soledad
Orihuela, Carla
Rodríguez, Rosalía
Acuña, Gonzalo
Rabaza, Victoria
Perg, Nancy
Cordero, Rossana
Reisfeld, Cristina
Olivera, Paula
Montero, Paola
Nogueira, Cecilia
Nalerio, Catheryn
Orihuela, Sergio
Curi, Lilián
Burgstaller, Ema
Noboa, Oscar
Pritsch, Otto
Nin, Marcelo
Bianchi, Sergio
Comparison of antibody response to SARS-CoV-2 after two doses of inactivated virus and BNT162b2 mRNA vaccines in kidney transplant
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 Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755301/
https://www.ncbi.nlm.nih.gov/pubmed/35198159
http://dx.doi.org/10.1093/ckj/sfab291
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