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Monocyte Receptors for Immunoglobulin and Complement in Immunologic Deficiency Diseases 1
Author(s) -
Douglas S. D.,
Goldberg L. S.
Publication year - 1972
Publication title -
vox sanguinis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.68
H-Index - 83
eISSN - 1423-0410
pISSN - 0042-9007
DOI - 10.1111/j.1423-0410.1972.tb04007.x
Subject(s) - wiskott–aldrich syndrome , chronic mucocutaneous candidiasis , immunology , monocyte , medicine , receptor , antibody , chronic granulomatous disease , primary immunodeficiency , immune system , disease , biology , pathology , biochemistry , gene
Summary Semiquantitative assessment of the human monocyte IgG receptor in normal subjects and patients with acquired agammaglobulinemia, chronic granulomatous disease chronic mucocutaneous candidiasis and the Wiskott‐Aldrich syndrome revealed no detectable differences. The monocyte C3 receptor was found to be normal in cells from patients with the Wiskott‐Aldrich syndrome. Monocyte receptors should be further investigated in patients with various forms of immunologic deficiency.