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Immunologic response of mRNA SARS-CoV-2 vaccination in adolescent kidney transplant recipients

BACKGROUND: In the general population, mRNA SARS-CoV-2 vaccines are highly efficacious. Early reports suggest a diminished antibody response in immunosuppressed adult solid organ transplant (SOT) patients, but this has not been reported in pediatrics. METHODS: Adolescent kidney transplant recipients...

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Autores principales: Crane, Clarkson, Phebus, Erin, Ingulli, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440151/
https://www.ncbi.nlm.nih.gov/pubmed/34522992
http://dx.doi.org/10.1007/s00467-021-05256-9
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author Crane, Clarkson
Phebus, Erin
Ingulli, Elizabeth
author_facet Crane, Clarkson
Phebus, Erin
Ingulli, Elizabeth
author_sort Crane, Clarkson
collection PubMed
description BACKGROUND: In the general population, mRNA SARS-CoV-2 vaccines are highly efficacious. Early reports suggest a diminished antibody response in immunosuppressed adult solid organ transplant (SOT) patients, but this has not been reported in pediatrics. METHODS: Adolescent kidney transplant recipients (KTR) at our center who received both doses of an mRNA SARS-CoV-2 vaccine had SARS-CoV-2 spike (S) protein antibody presence evaluated 4–8 weeks after their second dose of the vaccine as part of routine clinical care. RESULTS: Thirteen of 25 fully vaccinated patients (52%) had a positive spike antibody. Median age of participants was 19 years old (IQR 18–20) and the median time from transplant was 5 years (IQR 4–9 years). KTR were treated with an immunosuppression regimen including a calcineurin inhibitor, corticosteroid, and antimetabolite (9 with mycophenolate, 3 with azathioprine, and 1 without an antimetabolite due to viremia). Of those who had an antibody response, fewer had a mycophenolate-containing immunosuppressant regimen than non-responders. There was a trend toward better vaccine response and higher anti-S antibody titers at lower doses of mycophenolate. Three patients with prior COVID-19 infection all had a positive antibody response. CONCLUSION: Our results suggest vaccine response in adolescent KRT is lower than that of the general population, but similar to that previously described in adult SOT patients and slightly better than that seen in adult KTR. This data demonstrates vaccination is safe and supports immunizing KTR who remain hesitant. Future studies should focus on better understanding of the cellular immune response to vaccination and strategies to enhance vaccine immunogenicity in pediatric SOT patients. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-84401512021-09-15 Immunologic response of mRNA SARS-CoV-2 vaccination in adolescent kidney transplant recipients Crane, Clarkson Phebus, Erin Ingulli, Elizabeth Pediatr Nephrol Brief Report BACKGROUND: In the general population, mRNA SARS-CoV-2 vaccines are highly efficacious. Early reports suggest a diminished antibody response in immunosuppressed adult solid organ transplant (SOT) patients, but this has not been reported in pediatrics. METHODS: Adolescent kidney transplant recipients (KTR) at our center who received both doses of an mRNA SARS-CoV-2 vaccine had SARS-CoV-2 spike (S) protein antibody presence evaluated 4–8 weeks after their second dose of the vaccine as part of routine clinical care. RESULTS: Thirteen of 25 fully vaccinated patients (52%) had a positive spike antibody. Median age of participants was 19 years old (IQR 18–20) and the median time from transplant was 5 years (IQR 4–9 years). KTR were treated with an immunosuppression regimen including a calcineurin inhibitor, corticosteroid, and antimetabolite (9 with mycophenolate, 3 with azathioprine, and 1 without an antimetabolite due to viremia). Of those who had an antibody response, fewer had a mycophenolate-containing immunosuppressant regimen than non-responders. There was a trend toward better vaccine response and higher anti-S antibody titers at lower doses of mycophenolate. Three patients with prior COVID-19 infection all had a positive antibody response. CONCLUSION: Our results suggest vaccine response in adolescent KRT is lower than that of the general population, but similar to that previously described in adult SOT patients and slightly better than that seen in adult KTR. This data demonstrates vaccination is safe and supports immunizing KTR who remain hesitant. Future studies should focus on better understanding of the cellular immune response to vaccination and strategies to enhance vaccine immunogenicity in pediatric SOT patients. GRAPHICAL ABSTRACT: [Image: see text] Springer Berlin Heidelberg 2021-09-15 2022 /pmc/articles/PMC8440151/ /pubmed/34522992 http://dx.doi.org/10.1007/s00467-021-05256-9 Text en © IPNA 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Brief Report
Crane, Clarkson
Phebus, Erin
Ingulli, Elizabeth
Immunologic response of mRNA SARS-CoV-2 vaccination in adolescent kidney transplant recipients
title Immunologic response of mRNA SARS-CoV-2 vaccination in adolescent kidney transplant recipients
title_full Immunologic response of mRNA SARS-CoV-2 vaccination in adolescent kidney transplant recipients
title_fullStr Immunologic response of mRNA SARS-CoV-2 vaccination in adolescent kidney transplant recipients
title_full_unstemmed Immunologic response of mRNA SARS-CoV-2 vaccination in adolescent kidney transplant recipients
title_short Immunologic response of mRNA SARS-CoV-2 vaccination in adolescent kidney transplant recipients
title_sort immunologic response of mrna sars-cov-2 vaccination in adolescent kidney transplant recipients
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440151/
https://www.ncbi.nlm.nih.gov/pubmed/34522992
http://dx.doi.org/10.1007/s00467-021-05256-9
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