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A simplified assay for the specific diagnosis of paroxysmal nocturnal hemoglobinuria: detection of DAF(CD55)- and HRF20(CD59)- erythrocytes in microtyping cards.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Oncology, Radiology and Clinical Immunology.
1993 (English)In: Vox Sanguinis, ISSN 0042-9007, E-ISSN 1423-0410, Vol. 64, no 1, 43-46 p.Article in journal (Refereed) Published
Abstract [en]

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare disease that is caused by a monoclonal stem cell defect. The affected cells lack the carbohydrate linkage between phosphatidylinositol and a group of membrane proteins of which three protect the cell against complement lysis. The absence of these three proteins, DAF(CD55), C8BP and HRF20(CD59), makes cells from the erythropoiesis, thrombopoiesis and myelopoiesis extensively sensitive to complement attack and affected patients suffer from intravascular hemolysis, thrombosis and increased susceptibility to infections. In this study we describe a swift and specific assay for the detection of CD55- and CD59- erythrocytes, which is suitable for screening of possible PNH patients.

Place, publisher, year, edition, pages
1993. Vol. 64, no 1, 43-46 p.
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:uu:diva-265467PubMedID: 7680511OAI: oai:DiVA.org:uu-265467DiVA: diva2:865779
Available from: 2015-10-29 Created: 2015-10-29 Last updated: 2017-12-01

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