Literature DB >> 3779101

Morphological abnormalities in the lymphocytes of patients with the Wiskott-Aldrich syndrome.

D Kenney, L Cairns, E Remold-O'Donnell, J Peterson, F S Rosen, R Parkman.   

Abstract

Lymphocytes from 18 patients with the Wiskott-Aldrich Syndrome (WAS) were examined by scanning electron microscopy (SEM). Most peripheral blood lymphocytes from normal individuals are covered with slender microvillus projections, but a large proportion of lymphocytes from WAS patients were found to be relatively devoid of microvilli. A lymphocyte morphology scoring system was developed to quantify the density of microvilli: Grade 4 classified those lymphocytes with greater than 75% of the surface covered with microvilli with progressive decrements to grade 1, which were those without microvilli. The mean lymphocyte morphology score of eight normal individuals was 3.62 +/- .22. The mean lymphocyte score of WAS patients was substantially lower (2.89 +/- .27, P less than .001). In addition, WAS lymphocytes often were qualitatively abnormal, with short, blunted microvilli. These morphological criteria were used to diagnose WAS from the cord blood lymphocytes of one "at-risk" patient. Thus, WAS is the first primary immunodeficiency in which morphological abnormalities have been identified that can aid in diagnosis.

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Year:  1986        PMID: 3779101

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  38 in total

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Authors:  H D Ochs
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Review 2.  The Wiskott-Aldrich syndrome.

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Review 3.  Wiskott-Aldrich syndrome: a multidisciplinary disease.

Authors:  G R Standen
Journal:  J Clin Pathol       Date:  1991-12       Impact factor: 3.411

Review 4.  Genetics of human X-linked immunodeficiency diseases.

Authors:  R W Hendriks; R K Schuurman
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Review 5.  The Wiskott-Aldrich syndrome.

Authors:  H D Ochs
Journal:  Springer Semin Immunopathol       Date:  1998

6.  Mucin O-glycan branching enzymes: structure, function, and gene regulation.

Authors:  Pi-Wan Cheng; Prakash Radhakrishnan
Journal:  Adv Exp Med Biol       Date:  2011       Impact factor: 2.622

7.  Molecular characterization of sialophorin (CD43), the lymphocyte surface sialoglycoprotein defective in Wiskott-Aldrich syndrome.

Authors:  C S Shelley; E Remold-O'Donnell; A E Davis; G A Bruns; F S Rosen; M C Carroll; A S Whitehead
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

8.  A congenital activating mutant of WASp causes altered plasma membrane topography and adhesion under flow in lymphocytes.

Authors:  Siobhan O Burns; David J Killock; Dale A Moulding; Joao Metelo; Joao Nunes; Ruth R Taylor; Andrew Forge; Adrian J Thrasher; Aleksandar Ivetic
Journal:  Blood       Date:  2010-03-30       Impact factor: 22.113

9.  Molecular heterogeneity of a lymphocyte glycoprotein in immunodeficient patients.

Authors:  D Reisinger; R Parkman
Journal:  J Clin Invest       Date:  1987-02       Impact factor: 14.808

10.  Direct interaction of the Wiskott-Aldrich syndrome protein with the GTPase Cdc42.

Authors:  R Kolluri; K F Tolias; C L Carpenter; F S Rosen; T Kirchhausen
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-28       Impact factor: 11.205

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