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伴有具有抗-i活性的单克隆IgM(κ)的自身免疫性溶血性贫血。

Autoimmune hemolytic anemia in association with monoclonal IgM(kappa) with anti-i activity.

作者信息

Kay N E, Gordon L I, Douglas S D

出版信息

Am J Med. 1978 May;64(5):845-50. doi: 10.1016/0002-9343(78)90526-0.

Abstract

A patient with a warm autoimmune hemolytic anemia with an immunoglobulin G (IgG) panagglutinin, also had monocional IgM(kappa) cold agglutinin with anti-i activity. Ninety per cent of the peripheral blood lymphocytes had surface immunoglobulin and the number of T cells was diminished. A subpopulation of the patient's lymphocytes formed rosettes with cord (i) erythrocytes and not with adult (l) erythrocytes. The finding of increased lymphocytes bearing i-binding sites and a monoclonal antibody with anti-i activity could be related to shared idiotypic determinants between antigen-binding sites and serum antibody. The occurrence of two autoantibodies in this patient suggests an immune regulatory disorder.

摘要

一名患有温抗体型自身免疫性溶血性贫血且伴有免疫球蛋白G(IgG)全凝集素的患者,同时还具有单克隆IgM(κ)冷凝集素并带有抗-i活性。外周血淋巴细胞的90%具有表面免疫球蛋白,且T细胞数量减少。该患者淋巴细胞的一个亚群与脐血(i)红细胞形成玫瑰花结,而不与成人(I)红细胞形成玫瑰花结。发现带有i结合位点的淋巴细胞增多以及一种具有抗-i活性的单克隆抗体,这可能与抗原结合位点和血清抗体之间共享独特型决定簇有关。该患者出现两种自身抗体提示存在免疫调节紊乱。

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