Cargando…
Longitudinal assessment of HLA and MIC-A antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes
The significance of antibodies directed against paternal epitopes in the context of obstetric disorders is discussed controversially. In this study anti-HLA and anti-MIC-A antibodies were analysed in sera of women with uneventful pregnancy (n = 101), preeclampsia (PE, n = 55) and gestational diabete...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648869/ https://www.ncbi.nlm.nih.gov/pubmed/29051520 http://dx.doi.org/10.1038/s41598-017-13275-6 |
_version_ | 1783272459858870272 |
---|---|
author | Küssel, Lorenz Herkner, Harald Wahrmann, Markus Eskandary, Farsad Doberer, Konstantin Binder, Julia Pateisky, Petra Zeisler, Harald Böhmig, Georg A. Bond, Gregor |
author_facet | Küssel, Lorenz Herkner, Harald Wahrmann, Markus Eskandary, Farsad Doberer, Konstantin Binder, Julia Pateisky, Petra Zeisler, Harald Böhmig, Georg A. Bond, Gregor |
author_sort | Küssel, Lorenz |
collection | PubMed |
description | The significance of antibodies directed against paternal epitopes in the context of obstetric disorders is discussed controversially. In this study anti-HLA and anti-MIC-A antibodies were analysed in sera of women with uneventful pregnancy (n = 101), preeclampsia (PE, n = 55) and gestational diabetes (GDM, n = 36) using antigen specific microbeads. While two thirds of the women with uneventful pregnancy or GDM were HLA and MIC-A antibody positive in gestational week 11 to 13 with a modest increase towards the end of pregnancy, women with PE showed an inverse kinetic: 90% were HLA antibody positive in gestational week 11 to 13 and only 10% showed HLA reactivities at the end of the pregnancy. HLA antibody binding strength was more pronounced in gestational week 14 to 17 in patients with PE compared to women with uneventful pregnancy (maximum median fluorescence intensity of the highest ranked positive bead 7403, IQR 2193–7938 vs. 1093, IQR 395–5689; p = 0.04) and was able to predict PE with an AUC of 0.80 (95% CI 0.67–0.93; p = 0.002). Our data suggest a pathophysiological involvement of HLA antibodies in PE. HLA antibody quantification in early pregnancy may provide a useful tool to increase diagnostic awareness in women prone to develop PE. |
format | Online Article Text |
id | pubmed-5648869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56488692017-10-26 Longitudinal assessment of HLA and MIC-A antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes Küssel, Lorenz Herkner, Harald Wahrmann, Markus Eskandary, Farsad Doberer, Konstantin Binder, Julia Pateisky, Petra Zeisler, Harald Böhmig, Georg A. Bond, Gregor Sci Rep Article The significance of antibodies directed against paternal epitopes in the context of obstetric disorders is discussed controversially. In this study anti-HLA and anti-MIC-A antibodies were analysed in sera of women with uneventful pregnancy (n = 101), preeclampsia (PE, n = 55) and gestational diabetes (GDM, n = 36) using antigen specific microbeads. While two thirds of the women with uneventful pregnancy or GDM were HLA and MIC-A antibody positive in gestational week 11 to 13 with a modest increase towards the end of pregnancy, women with PE showed an inverse kinetic: 90% were HLA antibody positive in gestational week 11 to 13 and only 10% showed HLA reactivities at the end of the pregnancy. HLA antibody binding strength was more pronounced in gestational week 14 to 17 in patients with PE compared to women with uneventful pregnancy (maximum median fluorescence intensity of the highest ranked positive bead 7403, IQR 2193–7938 vs. 1093, IQR 395–5689; p = 0.04) and was able to predict PE with an AUC of 0.80 (95% CI 0.67–0.93; p = 0.002). Our data suggest a pathophysiological involvement of HLA antibodies in PE. HLA antibody quantification in early pregnancy may provide a useful tool to increase diagnostic awareness in women prone to develop PE. Nature Publishing Group UK 2017-10-19 /pmc/articles/PMC5648869/ /pubmed/29051520 http://dx.doi.org/10.1038/s41598-017-13275-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Küssel, Lorenz Herkner, Harald Wahrmann, Markus Eskandary, Farsad Doberer, Konstantin Binder, Julia Pateisky, Petra Zeisler, Harald Böhmig, Georg A. Bond, Gregor Longitudinal assessment of HLA and MIC-A antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes |
title | Longitudinal assessment of HLA and MIC-A antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes |
title_full | Longitudinal assessment of HLA and MIC-A antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes |
title_fullStr | Longitudinal assessment of HLA and MIC-A antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes |
title_full_unstemmed | Longitudinal assessment of HLA and MIC-A antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes |
title_short | Longitudinal assessment of HLA and MIC-A antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes |
title_sort | longitudinal assessment of hla and mic-a antibodies in uneventful pregnancies and pregnancies complicated by preeclampsia or gestational diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648869/ https://www.ncbi.nlm.nih.gov/pubmed/29051520 http://dx.doi.org/10.1038/s41598-017-13275-6 |
work_keys_str_mv | AT kussellorenz longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT herknerharald longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT wahrmannmarkus longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT eskandaryfarsad longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT dobererkonstantin longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT binderjulia longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT pateiskypetra longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT zeislerharald longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT bohmiggeorga longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes AT bondgregor longitudinalassessmentofhlaandmicaantibodiesinuneventfulpregnanciesandpregnanciescomplicatedbypreeclampsiaorgestationaldiabetes |