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Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women
Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection during pregnancy could result in adverse perinatal outcome. Clinical data on the assessment of the immune response in vaccinated pregnant women and subsequent transplacental antibody transfer are quite limited. Object...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778956/ https://www.ncbi.nlm.nih.gov/pubmed/35062762 http://dx.doi.org/10.3390/vaccines10010101 |
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author | Shen, Ching-Ju Fu, Yi-Chen Lin, Yen-Pin Shen, Ching-Fen Sun, Der-Ji Chen, Huan-Yun Cheng, Chao-Min |
author_facet | Shen, Ching-Ju Fu, Yi-Chen Lin, Yen-Pin Shen, Ching-Fen Sun, Der-Ji Chen, Huan-Yun Cheng, Chao-Min |
author_sort | Shen, Ching-Ju |
collection | PubMed |
description | Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection during pregnancy could result in adverse perinatal outcome. Clinical data on the assessment of the immune response in vaccinated pregnant women and subsequent transplacental antibody transfer are quite limited. Objective: To assess maternal and neonatal neutralizing antibody levels against both wildtype and Delta (B.1.617.2) variants after maternal mRNA vaccination. Study Design: This cohort study was conducted 29 pregnant women who were vaccinated at least one dose of Moderna (mRNA-1273) vaccine. Both neutralizing antibody (wildtype and Delta variant) and S1 receptor binding domain IgG antibody levels were evaluated in maternal and cord blood on the day of delivery. Results: Superiority of antibody level was significant in fully vaccinated women compared with the one-dose group (maternal sera, median, 97.46%; cord sera, median, 97.37% versus maternal sera, median, 4.01%; cord sera, median, 1.44%). No difference in antibody level was noted in relation to interval of second immunization to delivery in the two-dose group (95.99% in 0–2 weeks, 97.45% in 2–4 weeks, 97.48% in 4–8 weeks, 97.72% in 8–10 weeks). The most pronounced reduction was observed for the Delta variant. The wildtype neutralizing antibody level of full-vaccinated women was not influenced by the pertussis vaccination. Conclusion: The data underscore the importance of full vaccination in pregnancy and support the recommendation of COVID-19 immunization for pregnant women. The lower level of vaccine-induced neutralizing antibodies for the Delta variant indicates insufficient protection for mother and newborn and highlights the need for development of effective vaccine strategies. |
format | Online Article Text |
id | pubmed-8778956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87789562022-01-22 Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women Shen, Ching-Ju Fu, Yi-Chen Lin, Yen-Pin Shen, Ching-Fen Sun, Der-Ji Chen, Huan-Yun Cheng, Chao-Min Vaccines (Basel) Article Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection during pregnancy could result in adverse perinatal outcome. Clinical data on the assessment of the immune response in vaccinated pregnant women and subsequent transplacental antibody transfer are quite limited. Objective: To assess maternal and neonatal neutralizing antibody levels against both wildtype and Delta (B.1.617.2) variants after maternal mRNA vaccination. Study Design: This cohort study was conducted 29 pregnant women who were vaccinated at least one dose of Moderna (mRNA-1273) vaccine. Both neutralizing antibody (wildtype and Delta variant) and S1 receptor binding domain IgG antibody levels were evaluated in maternal and cord blood on the day of delivery. Results: Superiority of antibody level was significant in fully vaccinated women compared with the one-dose group (maternal sera, median, 97.46%; cord sera, median, 97.37% versus maternal sera, median, 4.01%; cord sera, median, 1.44%). No difference in antibody level was noted in relation to interval of second immunization to delivery in the two-dose group (95.99% in 0–2 weeks, 97.45% in 2–4 weeks, 97.48% in 4–8 weeks, 97.72% in 8–10 weeks). The most pronounced reduction was observed for the Delta variant. The wildtype neutralizing antibody level of full-vaccinated women was not influenced by the pertussis vaccination. Conclusion: The data underscore the importance of full vaccination in pregnancy and support the recommendation of COVID-19 immunization for pregnant women. The lower level of vaccine-induced neutralizing antibodies for the Delta variant indicates insufficient protection for mother and newborn and highlights the need for development of effective vaccine strategies. MDPI 2022-01-10 /pmc/articles/PMC8778956/ /pubmed/35062762 http://dx.doi.org/10.3390/vaccines10010101 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shen, Ching-Ju Fu, Yi-Chen Lin, Yen-Pin Shen, Ching-Fen Sun, Der-Ji Chen, Huan-Yun Cheng, Chao-Min Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women |
title | Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women |
title_full | Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women |
title_fullStr | Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women |
title_full_unstemmed | Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women |
title_short | Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women |
title_sort | evaluation of transplacental antibody transfer in sars-cov-2-immunized pregnant women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778956/ https://www.ncbi.nlm.nih.gov/pubmed/35062762 http://dx.doi.org/10.3390/vaccines10010101 |
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