Literature DB >> 1716964

The erythrocytes in paroxysmal nocturnal haemoglobinuria of intermediate sensitivity to complement lysis.

W F Rosse1, S Hoffman, M Campbell, M Borowitz, J O Moore, C J Parker.   

Abstract

The sensitivity to lysis by complement of the erythrocytes of 56 patients with paroxysmal nocturnal haemoglobinuria (PNH) was compared to the membrane expression of decay accelerating factor (DAF, CD55), membrane inhibitor of reactive lysis (MIRL, CD59) and acetylcholinesterase (AChE). Most patients (36/50 72% in whom the analysis could be made) appeared to have erythrocytes of intermediate sensitivity to complement in the blood. These cells appeared as a discrete population of cells (PNH II cells), as a 'tail' of cells slightly less sensitive than the predominant PNH III cells (previously called PNH IIIb cells), or as a continuous spectrum of cells sensitive to complement. The PNH III cells totally lacked all three proteins (DAF, MIRL, AChE) by flow cytometric analysis whereas PNH I cells appeared to have normal or nearly normal amounts of each. The cells of intermediate sensitivity (PNH II) had coordinately decreased expression of all three proteins; the level of expression of DAF and MIRL paralleled the sensitivity of the cells to the haemolytic action of complement.

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Year:  1991        PMID: 1716964     DOI: 10.1111/j.1365-2141.1991.tb08014.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  6 in total

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Journal:  Am J Blood Res       Date:  2016-08-05

Review 2.  Paroxysmal nocturnal hemoglobinuria and the glycosylphosphatidylinositol anchor.

Authors:  E T Yeh; W F Rosse
Journal:  J Clin Invest       Date:  1994-06       Impact factor: 14.808

3.  Paroxysmal nocturnal haemoglobinuria, diagnosis and haematological findings, first report from Iran, model for developing countries.

Authors:  Mohammadali Jahangirpour; Amirali Vahedi; Hamed Baghdadi; Tahereh Madani; Ali Behvarmanesh; Mohammad Alidadi; Mohadese Hashem Boroojerdi; Saba Mohammaei; Peyvand Poopak; Amirhossein Poopak; Gelareh Khosravi Pour; Behzad Poopak
Journal:  EJHaem       Date:  2022-03-08

4.  Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria.

Authors:  P Hillmen; M Bessler; P J Mason; W M Watkins; L Luzzatto
Journal:  Proc Natl Acad Sci U S A       Date:  1993-06-01       Impact factor: 11.205

5.  Technical advances in flow cytometry-based diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria.

Authors:  Rodolfo Patussi Correia; Laiz Cameirão Bento; Ana Carolina Apelle Bortolucci; Anderson Marega Alexandre; Andressa da Costa Vaz; Daniela Schimidell; Eduardo de Carvalho Pedro; Fabricio Simões Perin; Sonia Tsukasa Nozawa; Cláudio Ernesto Albers Mendes; Rodrigo de Souza Barroso; Nydia Strachman Bacal
Journal:  Einstein (Sao Paulo)       Date:  2016 Jul-Sep

6.  The frequency of granulocytes with spontaneous somatic mutations: a wide distribution in a normal human population.

Authors:  Tommaso Rondelli; Margherita Berardi; Benedetta Peruzzi; Luca Boni; Roberto Caporale; Piero Dolara; Rosario Notaro; Lucio Luzzatto
Journal:  PLoS One       Date:  2013-01-14       Impact factor: 3.240

  6 in total

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