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Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases
Yellow fever vaccine (YFV) is a live attenuated vaccine usually contraindicated for juvenile autoimmune rheumatic disease (JARD) patients. During the recent epidemic in Sao Paulo-Brazil, YFV was indicated for patients under low immunosuppression. Thirty JARD patients with inactive diseases undergoin...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686021/ https://www.ncbi.nlm.nih.gov/pubmed/34977552 http://dx.doi.org/10.1016/j.jvacx.2021.100131 |
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author | Emi Aikawa, Nádia Andrade Balbi, Verena Borba, Eduardo Ferreira Coracini Tonacio, Adriana Maluf Elias Sallum, Adriana Maria Arruda Campos, Lucia Tomie Kozu, Kátia Borges Vendramini, Margarete Fontoura, Nicole de Souza Azevedo, Adriana Dias Schwarcz, Waleska Marli Christovam Sartori, Ana Antonangelo, Leila Artur Silva, Clovis Bonfá, Eloisa |
author_facet | Emi Aikawa, Nádia Andrade Balbi, Verena Borba, Eduardo Ferreira Coracini Tonacio, Adriana Maluf Elias Sallum, Adriana Maria Arruda Campos, Lucia Tomie Kozu, Kátia Borges Vendramini, Margarete Fontoura, Nicole de Souza Azevedo, Adriana Dias Schwarcz, Waleska Marli Christovam Sartori, Ana Antonangelo, Leila Artur Silva, Clovis Bonfá, Eloisa |
author_sort | Emi Aikawa, Nádia |
collection | PubMed |
description | Yellow fever vaccine (YFV) is a live attenuated vaccine usually contraindicated for juvenile autoimmune rheumatic disease (JARD) patients. During the recent epidemic in Sao Paulo-Brazil, YFV was indicated for patients under low immunosuppression. Thirty JARD patients with inactive diseases undergoing low immunosuppression and 30 healthy controls (HC) were vaccinated with a fractional dose 17DD YFV (∼5495 IU) and evaluated 30 days later. JARD patients and controls had comparable median age (12.4 vs. 12 years, p = 0.250). Disease parameters remained stable 30 days after 17DD YFV (p > 0.05) and only mild adverse events were reported in both groups (p > 0.05). JARD and HC had similar seroprotection [93% vs. 100%;p = 0.49], seroconversion rates [96% vs. 100%;p = 0.489], and GMT [1249 vs.1293;p = 0.821]. Both groups had similar white-blood-cells kinetics with transient decreases in lymphocytes at D5 and neutrophils at D10, followed by full recovery at D30 (P < 0.05). In conclusion, 17DD YFV was safe and immunogenic in JARD. This study may contribute to recommendations for patients living/travelling to endemic areas. |
format | Online Article Text |
id | pubmed-8686021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86860212021-12-30 Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases Emi Aikawa, Nádia Andrade Balbi, Verena Borba, Eduardo Ferreira Coracini Tonacio, Adriana Maluf Elias Sallum, Adriana Maria Arruda Campos, Lucia Tomie Kozu, Kátia Borges Vendramini, Margarete Fontoura, Nicole de Souza Azevedo, Adriana Dias Schwarcz, Waleska Marli Christovam Sartori, Ana Antonangelo, Leila Artur Silva, Clovis Bonfá, Eloisa Vaccine X Short communication Yellow fever vaccine (YFV) is a live attenuated vaccine usually contraindicated for juvenile autoimmune rheumatic disease (JARD) patients. During the recent epidemic in Sao Paulo-Brazil, YFV was indicated for patients under low immunosuppression. Thirty JARD patients with inactive diseases undergoing low immunosuppression and 30 healthy controls (HC) were vaccinated with a fractional dose 17DD YFV (∼5495 IU) and evaluated 30 days later. JARD patients and controls had comparable median age (12.4 vs. 12 years, p = 0.250). Disease parameters remained stable 30 days after 17DD YFV (p > 0.05) and only mild adverse events were reported in both groups (p > 0.05). JARD and HC had similar seroprotection [93% vs. 100%;p = 0.49], seroconversion rates [96% vs. 100%;p = 0.489], and GMT [1249 vs.1293;p = 0.821]. Both groups had similar white-blood-cells kinetics with transient decreases in lymphocytes at D5 and neutrophils at D10, followed by full recovery at D30 (P < 0.05). In conclusion, 17DD YFV was safe and immunogenic in JARD. This study may contribute to recommendations for patients living/travelling to endemic areas. Elsevier 2021-12-10 /pmc/articles/PMC8686021/ /pubmed/34977552 http://dx.doi.org/10.1016/j.jvacx.2021.100131 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Short communication Emi Aikawa, Nádia Andrade Balbi, Verena Borba, Eduardo Ferreira Coracini Tonacio, Adriana Maluf Elias Sallum, Adriana Maria Arruda Campos, Lucia Tomie Kozu, Kátia Borges Vendramini, Margarete Fontoura, Nicole de Souza Azevedo, Adriana Dias Schwarcz, Waleska Marli Christovam Sartori, Ana Antonangelo, Leila Artur Silva, Clovis Bonfá, Eloisa Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases |
title | Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases |
title_full | Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases |
title_fullStr | Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases |
title_full_unstemmed | Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases |
title_short | Yellow fever vaccination in Brazil: Short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases |
title_sort | yellow fever vaccination in brazil: short-term safety and immunogenicity in juvenile autoimmune rheumatic diseases |
topic | Short communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686021/ https://www.ncbi.nlm.nih.gov/pubmed/34977552 http://dx.doi.org/10.1016/j.jvacx.2021.100131 |
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