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Fetomaternal alloimmunity as a cause of liver disease

Fetomaternal alloimmune disease has traditionally been associated with haematological disease such as fetomaternal alloimmune thrombocytopaenia and Rh haemolytic anaemia, but is now known to also be organ specific. Alloimmune membranous glomerulonephritis (AMG) is one of the most well understood org...

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Autores principales: Smyk, Daniel, Grammatikopoulos, Tassos, Daponte, Alexandros, Rigopoulou, Eirini I., Bogdanos, Dimitrios P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389071/
https://www.ncbi.nlm.nih.gov/pubmed/26000116
http://dx.doi.org/10.1007/s13317-011-0019-7
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author Smyk, Daniel
Grammatikopoulos, Tassos
Daponte, Alexandros
Rigopoulou, Eirini I.
Bogdanos, Dimitrios P.
author_facet Smyk, Daniel
Grammatikopoulos, Tassos
Daponte, Alexandros
Rigopoulou, Eirini I.
Bogdanos, Dimitrios P.
author_sort Smyk, Daniel
collection PubMed
description Fetomaternal alloimmune disease has traditionally been associated with haematological disease such as fetomaternal alloimmune thrombocytopaenia and Rh haemolytic anaemia, but is now known to also be organ specific. Alloimmune membranous glomerulonephritis (AMG) is one of the most well understood organ-specific alloimmune diseases. Neonatal haemochromatosis (NH) is a rare condition characterised by early liver failure in infants, with evidence suggesting that it is also alloimmune. Both AMG and NH appear to involve the passive transfer of alloantibodies to the fetus, which bind a specific alloantigen, fix complement and activate the terminal complement cascade. Although differences between AMG and NH are known, and evidence of the presence of antigen-specific alloantibodies in NH is still missing, we will use AMG as an example of fetomaternal organ specific alloimmune disease, and critically compare this to other emerging evidence that indicates that NH is also alloimmune.
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spelling pubmed-43890712015-05-21 Fetomaternal alloimmunity as a cause of liver disease Smyk, Daniel Grammatikopoulos, Tassos Daponte, Alexandros Rigopoulou, Eirini I. Bogdanos, Dimitrios P. Auto Immun Highlights Review Article Fetomaternal alloimmune disease has traditionally been associated with haematological disease such as fetomaternal alloimmune thrombocytopaenia and Rh haemolytic anaemia, but is now known to also be organ specific. Alloimmune membranous glomerulonephritis (AMG) is one of the most well understood organ-specific alloimmune diseases. Neonatal haemochromatosis (NH) is a rare condition characterised by early liver failure in infants, with evidence suggesting that it is also alloimmune. Both AMG and NH appear to involve the passive transfer of alloantibodies to the fetus, which bind a specific alloantigen, fix complement and activate the terminal complement cascade. Although differences between AMG and NH are known, and evidence of the presence of antigen-specific alloantibodies in NH is still missing, we will use AMG as an example of fetomaternal organ specific alloimmune disease, and critically compare this to other emerging evidence that indicates that NH is also alloimmune. Springer International Publishing 2011-03-23 /pmc/articles/PMC4389071/ /pubmed/26000116 http://dx.doi.org/10.1007/s13317-011-0019-7 Text en © Springer-Verlag 2011
spellingShingle Review Article
Smyk, Daniel
Grammatikopoulos, Tassos
Daponte, Alexandros
Rigopoulou, Eirini I.
Bogdanos, Dimitrios P.
Fetomaternal alloimmunity as a cause of liver disease
title Fetomaternal alloimmunity as a cause of liver disease
title_full Fetomaternal alloimmunity as a cause of liver disease
title_fullStr Fetomaternal alloimmunity as a cause of liver disease
title_full_unstemmed Fetomaternal alloimmunity as a cause of liver disease
title_short Fetomaternal alloimmunity as a cause of liver disease
title_sort fetomaternal alloimmunity as a cause of liver disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389071/
https://www.ncbi.nlm.nih.gov/pubmed/26000116
http://dx.doi.org/10.1007/s13317-011-0019-7
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