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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Fetomaternal alloimmunity as a cause of liver disease

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Author
Smyk, D.; Grammatikopoulos, T.; Daponte, A.; Rigopoulou, E. I.; Bogdanos, D. P.
Date
2011
DOI
10.1007/s13317-011-0019-7
Keyword
Alloimmune
Autoimmunity
Immunisation
Intravenous immunoglobulin
Placenta
immunoglobulin
immunoglobulin G1
immunoglobulin G3
maternal antibody
membrane metalloendopeptidase
membrane metalloendopeptidase antibody
mitochondrion antibody
unclassified drug
alloimmune membranous glomerulonephritis
alloimmunization
antibody production
fetomaternal alloimmune disease
gestational age
hemochromatosis
human
immunoblotting
kidney disease
liver biopsy
liver disease
liver function
liver injury
membranous glomerulonephritis
neonatal hemochromatosis
neonatal liver disease
newborn disease
nonhuman
pathogenesis
priority journal
review
Metadata display
Abstract
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. © 2011 Springer-Verlag.
URI
http://hdl.handle.net/11615/33106
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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