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Anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages

BACKGROUND: We recently demonstrated the increased abundance of anti-trophoblast antibodies (ATAB) in sera of patients with unexplained recurrent miscarriages (uRM). Further, the ATAB-positive sera bound to JEG-3 human choriocarcinoma cells in vitro, resulting in decreased productions of β-human cho...

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Autores principales: Ye, Yao, Kuhn, Christina, Kösters, Miwako, Arnold, Georg J., Ishikawa-Ankerhold, Hellen, Schulz, Christian, Rogenhofer, Nina, Thaler, Christian J., Mahner, Sven, Fröhlich, Thomas, Jeschke, Udo, von Schönfeldt, Viktoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444073/
https://www.ncbi.nlm.nih.gov/pubmed/30827932
http://dx.doi.org/10.1016/j.ebiom.2019.02.027
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author Ye, Yao
Kuhn, Christina
Kösters, Miwako
Arnold, Georg J.
Ishikawa-Ankerhold, Hellen
Schulz, Christian
Rogenhofer, Nina
Thaler, Christian J.
Mahner, Sven
Fröhlich, Thomas
Jeschke, Udo
von Schönfeldt, Viktoria
author_facet Ye, Yao
Kuhn, Christina
Kösters, Miwako
Arnold, Georg J.
Ishikawa-Ankerhold, Hellen
Schulz, Christian
Rogenhofer, Nina
Thaler, Christian J.
Mahner, Sven
Fröhlich, Thomas
Jeschke, Udo
von Schönfeldt, Viktoria
author_sort Ye, Yao
collection PubMed
description BACKGROUND: We recently demonstrated the increased abundance of anti-trophoblast antibodies (ATAB) in sera of patients with unexplained recurrent miscarriages (uRM). Further, the ATAB-positive sera bound to JEG-3 human choriocarcinoma cells in vitro, resulting in decreased productions of β-human chorionic gonadotropin (β-hCG) and progesterone in these cells. However, the specific antigenic epitopes of ATAB have remained unknown. Therefore, it was the aim of this study to determine specific targets of ATAB in uRM patients. METHODS: Potential targets of ATAB were analyzed by 2-dimensional difference gel electrophoresis (2D-DIGE) and mass spectrometry, and thereby identifying α-Enolase (ENO1). ATAB targeting of ENO1 was further confirmed in a competitive binding assay. Levels of anti-ENO1 antibodies as well as β-hCG and progesterone were quantified with enzyme-linked immunosorbent assay (ELISA). Additionally, expression of ENO1 was analyzed in first trimester placentas by immunohistochemistry and immunofluorescence analysis. FINDINGS: We here identified ENO1 as a prominent target of ATAB. Serum levels of anti-ENO1 antibodies were increased in ATAB-positive compared to ATAB-negative patients. Further, increased expression of ENO1 and its co-expression with β-arrestin was found in the extra villous trophoblasts of uRM patients in first trimester placentas. In vitro, anti-ENO1 antibodies decreased the secretion of β-hCG and progesterone in JEG-3 and primary human villous trophoblast cells. INTERPRETATION: Serum anti-ENO1 antibodies might be an autoimmune biomarker for uRM. Targeting the formation of anti-ENO1 antibodies or inhibition of ENO1 expression could potentially represent therapeutic strategies for these patients. FUND: All authors declare no conflict of interest. Yao Ye was supported by the China Scholarship Council. Hellen Ishikawa-Ankerhold and Christian Schulz were supported by the SFB914, projects Z01 and A10. None of the rest authors has any conflict of interest to declare.
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spelling pubmed-64440732019-04-11 Anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages Ye, Yao Kuhn, Christina Kösters, Miwako Arnold, Georg J. Ishikawa-Ankerhold, Hellen Schulz, Christian Rogenhofer, Nina Thaler, Christian J. Mahner, Sven Fröhlich, Thomas Jeschke, Udo von Schönfeldt, Viktoria EBioMedicine Research paper BACKGROUND: We recently demonstrated the increased abundance of anti-trophoblast antibodies (ATAB) in sera of patients with unexplained recurrent miscarriages (uRM). Further, the ATAB-positive sera bound to JEG-3 human choriocarcinoma cells in vitro, resulting in decreased productions of β-human chorionic gonadotropin (β-hCG) and progesterone in these cells. However, the specific antigenic epitopes of ATAB have remained unknown. Therefore, it was the aim of this study to determine specific targets of ATAB in uRM patients. METHODS: Potential targets of ATAB were analyzed by 2-dimensional difference gel electrophoresis (2D-DIGE) and mass spectrometry, and thereby identifying α-Enolase (ENO1). ATAB targeting of ENO1 was further confirmed in a competitive binding assay. Levels of anti-ENO1 antibodies as well as β-hCG and progesterone were quantified with enzyme-linked immunosorbent assay (ELISA). Additionally, expression of ENO1 was analyzed in first trimester placentas by immunohistochemistry and immunofluorescence analysis. FINDINGS: We here identified ENO1 as a prominent target of ATAB. Serum levels of anti-ENO1 antibodies were increased in ATAB-positive compared to ATAB-negative patients. Further, increased expression of ENO1 and its co-expression with β-arrestin was found in the extra villous trophoblasts of uRM patients in first trimester placentas. In vitro, anti-ENO1 antibodies decreased the secretion of β-hCG and progesterone in JEG-3 and primary human villous trophoblast cells. INTERPRETATION: Serum anti-ENO1 antibodies might be an autoimmune biomarker for uRM. Targeting the formation of anti-ENO1 antibodies or inhibition of ENO1 expression could potentially represent therapeutic strategies for these patients. FUND: All authors declare no conflict of interest. Yao Ye was supported by the China Scholarship Council. Hellen Ishikawa-Ankerhold and Christian Schulz were supported by the SFB914, projects Z01 and A10. None of the rest authors has any conflict of interest to declare. Elsevier 2019-03-01 /pmc/articles/PMC6444073/ /pubmed/30827932 http://dx.doi.org/10.1016/j.ebiom.2019.02.027 Text en © 2019 The Authors http://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 Research paper
Ye, Yao
Kuhn, Christina
Kösters, Miwako
Arnold, Georg J.
Ishikawa-Ankerhold, Hellen
Schulz, Christian
Rogenhofer, Nina
Thaler, Christian J.
Mahner, Sven
Fröhlich, Thomas
Jeschke, Udo
von Schönfeldt, Viktoria
Anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages
title Anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages
title_full Anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages
title_fullStr Anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages
title_full_unstemmed Anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages
title_short Anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages
title_sort anti α-enolase antibody is a novel autoimmune biomarker for unexplained recurrent miscarriages
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444073/
https://www.ncbi.nlm.nih.gov/pubmed/30827932
http://dx.doi.org/10.1016/j.ebiom.2019.02.027
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