Autoantibodies in sporadic porphyria cutanea tarda
Jazyk angličtina Médium print-electronic
Typ dokumentu časopisecké články
- MeSH
- antigeny imunologie MeSH
- antinukleární protilátky analýza imunologie MeSH
- autoprotilátky analýza fyziologie MeSH
- cytosol imunologie MeSH
- fluorescenční protilátková technika nepřímá MeSH
- hepatitida C - protilátky analýza MeSH
- imunoblotting MeSH
- játra imunologie MeSH
- koproporfyriny moč MeSH
- lidé MeSH
- osmolární koncentrace MeSH
- porfyriny moč MeSH
- porphyria cutanea tarda imunologie moč MeSH
- uroporfyrinogendekarboxylasa antagonisté a inhibitory MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antigeny MeSH
- antinukleární protilátky MeSH
- autoprotilátky MeSH
- hepatitida C - protilátky MeSH
- koproporfyriny MeSH
- porfyriny MeSH
- uroporfyrinogendekarboxylasa MeSH
In an investigation of autoimmune antibodies using indirect immunofluorescence and Western blot analysis in a group of porphyria cutanea tarda patients we did not find any cytosolic antibodies potentially able to inhibit uroporphyrinogen decarboxylase. Furthermore, no known etiological factors were present in any of our patients. We therefore consider the development of the recently reported autoantibody with a molecular weight of 40 kDa a reaction to infection with the hepatitis C virus. The origin of mostly antinuclear antibodies against liver antigens (50, 45 and 56 kDa), detected in seven patients, was not identified and their etiopathogenetic implications remain unknown.
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