PRIMARY ACQUIRED AGAMMAGLOBULINEMIA ASSOCIATED WITH EPILEPSY
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چکیده
منابع مشابه
Antihelper T cell autoantibody in acquired agammaglobulinemia.
A patient with acquired agammaglobulinemia had an antihelper T cell factor that was identified as an immunoglobulin of the IgG class. The factor specifically bound to the TH2- T cell subset and, in the presence of complement, abolished the helper effect of normal T cells. The antihelper T cell antibody preceded by several years the appearance of suppressor TH2+Ia+ T cells, at which time the cli...
متن کاملA genetic defect in "acquired" agammaglobulinemia.
Phytohemagglutinin (PHA) has been shown to effect biochemical and morphologic changes in the small lymphocytes of normal human peripheral blood.1' 2 The percentage of morphologic transformation of small lymphocytes to blastlike cells on exposure to PHA is reduced in a variety of conditions associated with abnormalities of the lymphoid system, such as Hodgkin's disease, sarcoidosis, and chronic ...
متن کاملneutropenia associated with x-linked agammaglobulinemia
x-linked agammaglobulinemia (xla) is a hereditary immunodeficiency, characterized by an early onset of recurrent bacterial infections, hypogammaglobulinemia and markedly reduced b lymphocytes number. in order to determine the association of neutropenia among iranian patients with xla, hospital records of 30 patients with confirmed xla in children medical center hospital, were reviewed. eight ou...
متن کاملDefective RNA Synthesis in Lymphocytes from Patients with Primary Agammaglobulinemia.
Addition of tetanus toxoid to sensitized lymphocytes from normal subjects and patients with "secondary" acquired agammaglobulinemia resulted in an increased incorporation of tritiated uridine into RNA and this increase was sustained for 48 to 72 hours in vitro. In contrast, the quantity of H(3)-uridine incorporated into the RNA of lymphocytes from patients with "primary" acquired agammaglobulin...
متن کاملPartial immunologic reconstitution of a patient with acquired agammaglobulinemia: a transient phenomenon accompanying therapeutic plasmapheresis.
A patient with acquired agammaglobulinemia was treated with plasmapheresis. The rationale for this procedure was based on the presence of a cytotoxic autoantibody with specificity for helper (TH2-) T lymphocytes. Plasmapheresis reduced the autoantibody concentration to undetectable levels, which resulted in an increase number of helper T cells. These T cells provided normal in vitro helper acti...
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ژورنال
عنوان ژورنال: Nihon Naika Gakkai Zasshi
سال: 1974
ISSN: 0021-5384,1883-2083
DOI: 10.2169/naika.63.49