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Maternal Immune Response to ZIKV Triggers High-Inflammatory Profile in Congenital Zika Syndrome
The immunological mechanisms involved in the development of congenital Zika syndrome (CZS) have yet to be fully clarified. This study aims to assess the immuno-inflammatory profile of mothers and their children who have been diagnosed with CZS. Blood samples, which were confirmed clinically using th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9866085/ https://www.ncbi.nlm.nih.gov/pubmed/36680261 http://dx.doi.org/10.3390/v15010220 |
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author | Fialho, Eder M. S. Veras, Emanoel M. de Jesus, Caroline M. Khouri, Ricardo Sousa, Patrícia S. Ribeiro, Marizelia R. C. Costa, Luciana C. Gomes, Líllian N. Nascimento, Flávia R. F. Silva, Antônio A. M. Soeiro-Pereira, Paulo V. |
author_facet | Fialho, Eder M. S. Veras, Emanoel M. de Jesus, Caroline M. Khouri, Ricardo Sousa, Patrícia S. Ribeiro, Marizelia R. C. Costa, Luciana C. Gomes, Líllian N. Nascimento, Flávia R. F. Silva, Antônio A. M. Soeiro-Pereira, Paulo V. |
author_sort | Fialho, Eder M. S. |
collection | PubMed |
description | The immunological mechanisms involved in the development of congenital Zika syndrome (CZS) have yet to be fully clarified. This study aims to assess the immuno-inflammatory profile of mothers and their children who have been diagnosed with CZS. Blood samples, which were confirmed clinically using the plaque reduction neutralization test (PRNT), were collected from children with CZS and their mothers (CZS+ group). Samples were also collected from children who did not develop CZS and had a negative PRNT result and from their mothers (CZS- group). The data demonstrated a correlation between the leukocyte profile of CZS+ children and their mothers, more evident in monocytes. Monocytes from mothers of CZS+ children showed low expression of HLA and elevated hydrogen peroxide production. CZS+ children presented standard HLA expression and a higher hydrogen peroxide concentration than CZS- children. Monocyte superoxide dismutase activity remained functional. Moreover, when assessing the monocyte polarization, it was observed that there was no difference in nitrite concentrations; however, there was a decrease in arginase activity in CZS+ children. These data suggest that ZIKV infection induces a maternal immuno-inflammatory background related to the child’s inflammatory response after birth, possibly affecting the development and progression of congenital Zika syndrome. |
format | Online Article Text |
id | pubmed-9866085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98660852023-01-22 Maternal Immune Response to ZIKV Triggers High-Inflammatory Profile in Congenital Zika Syndrome Fialho, Eder M. S. Veras, Emanoel M. de Jesus, Caroline M. Khouri, Ricardo Sousa, Patrícia S. Ribeiro, Marizelia R. C. Costa, Luciana C. Gomes, Líllian N. Nascimento, Flávia R. F. Silva, Antônio A. M. Soeiro-Pereira, Paulo V. Viruses Article The immunological mechanisms involved in the development of congenital Zika syndrome (CZS) have yet to be fully clarified. This study aims to assess the immuno-inflammatory profile of mothers and their children who have been diagnosed with CZS. Blood samples, which were confirmed clinically using the plaque reduction neutralization test (PRNT), were collected from children with CZS and their mothers (CZS+ group). Samples were also collected from children who did not develop CZS and had a negative PRNT result and from their mothers (CZS- group). The data demonstrated a correlation between the leukocyte profile of CZS+ children and their mothers, more evident in monocytes. Monocytes from mothers of CZS+ children showed low expression of HLA and elevated hydrogen peroxide production. CZS+ children presented standard HLA expression and a higher hydrogen peroxide concentration than CZS- children. Monocyte superoxide dismutase activity remained functional. Moreover, when assessing the monocyte polarization, it was observed that there was no difference in nitrite concentrations; however, there was a decrease in arginase activity in CZS+ children. These data suggest that ZIKV infection induces a maternal immuno-inflammatory background related to the child’s inflammatory response after birth, possibly affecting the development and progression of congenital Zika syndrome. MDPI 2023-01-13 /pmc/articles/PMC9866085/ /pubmed/36680261 http://dx.doi.org/10.3390/v15010220 Text en © 2023 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 Fialho, Eder M. S. Veras, Emanoel M. de Jesus, Caroline M. Khouri, Ricardo Sousa, Patrícia S. Ribeiro, Marizelia R. C. Costa, Luciana C. Gomes, Líllian N. Nascimento, Flávia R. F. Silva, Antônio A. M. Soeiro-Pereira, Paulo V. Maternal Immune Response to ZIKV Triggers High-Inflammatory Profile in Congenital Zika Syndrome |
title | Maternal Immune Response to ZIKV Triggers High-Inflammatory Profile in Congenital Zika Syndrome |
title_full | Maternal Immune Response to ZIKV Triggers High-Inflammatory Profile in Congenital Zika Syndrome |
title_fullStr | Maternal Immune Response to ZIKV Triggers High-Inflammatory Profile in Congenital Zika Syndrome |
title_full_unstemmed | Maternal Immune Response to ZIKV Triggers High-Inflammatory Profile in Congenital Zika Syndrome |
title_short | Maternal Immune Response to ZIKV Triggers High-Inflammatory Profile in Congenital Zika Syndrome |
title_sort | maternal immune response to zikv triggers high-inflammatory profile in congenital zika syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9866085/ https://www.ncbi.nlm.nih.gov/pubmed/36680261 http://dx.doi.org/10.3390/v15010220 |
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