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High Levels of CXCL8 and Low Levels of CXCL9 and CXCL10 in Women with Maternal RhD Alloimmunization
Maternal RhD alloimmunization is an inflammatory response against protein antigens in fetal red blood cells (RBC). However, not all women become alloimmunized when exposed to RhD(+) fetal RBC. Thus, this study aimed to evaluate levels of inflammatory chemokines in RhD(−) pregnant women with erythroc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494496/ https://www.ncbi.nlm.nih.gov/pubmed/28717357 http://dx.doi.org/10.3389/fimmu.2017.00700 |
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author | Schettini, Juliana Araújo de Carvalho Gomes, Thomás Virgílio Santos Barreto, Alexandra Karla da Silva Júnior, Claudeir Dias da Matta, Marina Coutinho, Isabela Cristina Neiva de Oliveira, Maria do Carmo Valgueiro Costa Torres, Leuridan Cavalcante |
author_facet | Schettini, Juliana Araújo de Carvalho Gomes, Thomás Virgílio Santos Barreto, Alexandra Karla da Silva Júnior, Claudeir Dias da Matta, Marina Coutinho, Isabela Cristina Neiva de Oliveira, Maria do Carmo Valgueiro Costa Torres, Leuridan Cavalcante |
author_sort | Schettini, Juliana Araújo de Carvalho |
collection | PubMed |
description | Maternal RhD alloimmunization is an inflammatory response against protein antigens in fetal red blood cells (RBC). However, not all women become alloimmunized when exposed to RhD(+) fetal RBC. Thus, this study aimed to evaluate levels of inflammatory chemokines in RhD(−) pregnant women with erythrocyte alloimmunization. CXCL8, CXCL9, CCL5, and CXCL10 levels were determined from cell culture supernatants by flow cytometry in 46 (30 non-alloimmunized RhD(−) and 16 previously alloimmunized RhD(−)) pregnant women. CXCL8 levels were significantly higher (P < 0.004), and CXCL9 (P < 0.008) and CXCL10 (P < 0.003) levels were significantly lower in alloimmunized pregnant women. No significant difference in CCL5 levels was detected between the groups. Fetal RHD genotyping was performed in the alloimmunized RhD(−) group by real-time PCR. Anti-D alloantibody was detected in 10 mothers and anti-D and -C in six mothers. Twelve fetuses were RHD positive and four were RHD negative. Further studies of serum chemokines and placenta tissue could provide a better understanding of the cells involved in the pathogenesis of maternal erythrocyte alloimmunization. |
format | Online Article Text |
id | pubmed-5494496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54944962017-07-17 High Levels of CXCL8 and Low Levels of CXCL9 and CXCL10 in Women with Maternal RhD Alloimmunization Schettini, Juliana Araújo de Carvalho Gomes, Thomás Virgílio Santos Barreto, Alexandra Karla da Silva Júnior, Claudeir Dias da Matta, Marina Coutinho, Isabela Cristina Neiva de Oliveira, Maria do Carmo Valgueiro Costa Torres, Leuridan Cavalcante Front Immunol Immunology Maternal RhD alloimmunization is an inflammatory response against protein antigens in fetal red blood cells (RBC). However, not all women become alloimmunized when exposed to RhD(+) fetal RBC. Thus, this study aimed to evaluate levels of inflammatory chemokines in RhD(−) pregnant women with erythrocyte alloimmunization. CXCL8, CXCL9, CCL5, and CXCL10 levels were determined from cell culture supernatants by flow cytometry in 46 (30 non-alloimmunized RhD(−) and 16 previously alloimmunized RhD(−)) pregnant women. CXCL8 levels were significantly higher (P < 0.004), and CXCL9 (P < 0.008) and CXCL10 (P < 0.003) levels were significantly lower in alloimmunized pregnant women. No significant difference in CCL5 levels was detected between the groups. Fetal RHD genotyping was performed in the alloimmunized RhD(−) group by real-time PCR. Anti-D alloantibody was detected in 10 mothers and anti-D and -C in six mothers. Twelve fetuses were RHD positive and four were RHD negative. Further studies of serum chemokines and placenta tissue could provide a better understanding of the cells involved in the pathogenesis of maternal erythrocyte alloimmunization. Frontiers Media S.A. 2017-07-03 /pmc/articles/PMC5494496/ /pubmed/28717357 http://dx.doi.org/10.3389/fimmu.2017.00700 Text en Copyright © 2017 Schettini, Gomes, Santos Barreto, Silva Júnior, Matta, Coutinho, Oliveira and Torres. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Schettini, Juliana Araújo de Carvalho Gomes, Thomás Virgílio Santos Barreto, Alexandra Karla da Silva Júnior, Claudeir Dias da Matta, Marina Coutinho, Isabela Cristina Neiva de Oliveira, Maria do Carmo Valgueiro Costa Torres, Leuridan Cavalcante High Levels of CXCL8 and Low Levels of CXCL9 and CXCL10 in Women with Maternal RhD Alloimmunization |
title | High Levels of CXCL8 and Low Levels of CXCL9 and CXCL10 in Women with Maternal RhD Alloimmunization |
title_full | High Levels of CXCL8 and Low Levels of CXCL9 and CXCL10 in Women with Maternal RhD Alloimmunization |
title_fullStr | High Levels of CXCL8 and Low Levels of CXCL9 and CXCL10 in Women with Maternal RhD Alloimmunization |
title_full_unstemmed | High Levels of CXCL8 and Low Levels of CXCL9 and CXCL10 in Women with Maternal RhD Alloimmunization |
title_short | High Levels of CXCL8 and Low Levels of CXCL9 and CXCL10 in Women with Maternal RhD Alloimmunization |
title_sort | high levels of cxcl8 and low levels of cxcl9 and cxcl10 in women with maternal rhd alloimmunization |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494496/ https://www.ncbi.nlm.nih.gov/pubmed/28717357 http://dx.doi.org/10.3389/fimmu.2017.00700 |
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