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Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study
BACKGROUND: : Solid organ transplant recipients (SOTRs) are susceptible to severe coronavirus disease 2019 (COVID-19); however, immunogenicity studies of the Omicron variants per vaccination schedules are still lacking. We examined humoral immunogenicity following third-dose mRNA vaccine administrat...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800015/ https://www.ncbi.nlm.nih.gov/pubmed/36592547 http://dx.doi.org/10.1016/j.jcv.2022.105374 |
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author | Kang, Ji-Man Lee, Juhan Huh, Kyu Ha Joo, Dong Jin Lee, Jae Geun Kim, Ha Yan Lee, Myeongjee Jung, Inkyung Kim, Min Young Kim, Sinyoung Park, Younhee Kim, Myoung Soo |
author_facet | Kang, Ji-Man Lee, Juhan Huh, Kyu Ha Joo, Dong Jin Lee, Jae Geun Kim, Ha Yan Lee, Myeongjee Jung, Inkyung Kim, Min Young Kim, Sinyoung Park, Younhee Kim, Myoung Soo |
author_sort | Kang, Ji-Man |
collection | PubMed |
description | BACKGROUND: : Solid organ transplant recipients (SOTRs) are susceptible to severe coronavirus disease 2019 (COVID-19); however, immunogenicity studies of the Omicron variants per vaccination schedules are still lacking. We examined humoral immunogenicity following third-dose mRNA vaccine administration in Korean SOTRs who received primary COVID-19 vaccine series on homologous or heterologous schedules. METHODS: : We recruited SOTRs at Severance Hospital from October 27, 2021, to March 31, 2022. Blood samples were collected between 14 days and 5 months after the second and third mRNA vaccine (BNT162b2 or mRNA-1273) doses. SARS-CoV-2 anti-spike IgG titer was analyzed. The neutralization inhibition rate was analyzed using the surrogate neutralization assay for the wild-type, Delta, and Omicron variants. RESULTS: : No significant differences existed in the SARS-CoV-2 anti-spike IgG positivity rate between the homologous BNT162b2/BNT162b2/BNT162b2 (85%) and other heterologous groups (83% of ChAdOx1/ChAdOx1/BNT162b2, 90% of ChAdOx1/ChAdOx1/mRNA-1273, and 78% of ChAdOx1/BNT162b2/BNT162b2). No significant difference existed in the neutralization inhibition rates between the four groups for wild-type, Delta, and Omicron variants. Median neutralization inhibition rates against the Omicron variant (2–5%) were significantly lower than those against the wild-type (87–97%) and Delta (55–89%) variants (P < 0.001). CONCLUSIONS: : Regardless of the schedule, the neutralization inhibition rate against the Omicron variant was poor; therefore, additional preventive measures are required in such high-risk populations. |
format | Online Article Text |
id | pubmed-9800015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98000152022-12-30 Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study Kang, Ji-Man Lee, Juhan Huh, Kyu Ha Joo, Dong Jin Lee, Jae Geun Kim, Ha Yan Lee, Myeongjee Jung, Inkyung Kim, Min Young Kim, Sinyoung Park, Younhee Kim, Myoung Soo J Clin Virol Article BACKGROUND: : Solid organ transplant recipients (SOTRs) are susceptible to severe coronavirus disease 2019 (COVID-19); however, immunogenicity studies of the Omicron variants per vaccination schedules are still lacking. We examined humoral immunogenicity following third-dose mRNA vaccine administration in Korean SOTRs who received primary COVID-19 vaccine series on homologous or heterologous schedules. METHODS: : We recruited SOTRs at Severance Hospital from October 27, 2021, to March 31, 2022. Blood samples were collected between 14 days and 5 months after the second and third mRNA vaccine (BNT162b2 or mRNA-1273) doses. SARS-CoV-2 anti-spike IgG titer was analyzed. The neutralization inhibition rate was analyzed using the surrogate neutralization assay for the wild-type, Delta, and Omicron variants. RESULTS: : No significant differences existed in the SARS-CoV-2 anti-spike IgG positivity rate between the homologous BNT162b2/BNT162b2/BNT162b2 (85%) and other heterologous groups (83% of ChAdOx1/ChAdOx1/BNT162b2, 90% of ChAdOx1/ChAdOx1/mRNA-1273, and 78% of ChAdOx1/BNT162b2/BNT162b2). No significant difference existed in the neutralization inhibition rates between the four groups for wild-type, Delta, and Omicron variants. Median neutralization inhibition rates against the Omicron variant (2–5%) were significantly lower than those against the wild-type (87–97%) and Delta (55–89%) variants (P < 0.001). CONCLUSIONS: : Regardless of the schedule, the neutralization inhibition rate against the Omicron variant was poor; therefore, additional preventive measures are required in such high-risk populations. Elsevier B.V. 2023-02 2022-12-30 /pmc/articles/PMC9800015/ /pubmed/36592547 http://dx.doi.org/10.1016/j.jcv.2022.105374 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Kang, Ji-Man Lee, Juhan Huh, Kyu Ha Joo, Dong Jin Lee, Jae Geun Kim, Ha Yan Lee, Myeongjee Jung, Inkyung Kim, Min Young Kim, Sinyoung Park, Younhee Kim, Myoung Soo Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study |
title | Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study |
title_full | Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study |
title_fullStr | Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study |
title_full_unstemmed | Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study |
title_short | Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study |
title_sort | comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mrna vaccine with homologous or heterologous schedules: an observational study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800015/ https://www.ncbi.nlm.nih.gov/pubmed/36592547 http://dx.doi.org/10.1016/j.jcv.2022.105374 |
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