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体外蛋白A免疫吸附对一名免疫性血小板减少性紫癜患者独特型和抗独特型免疫球蛋白G反应的调节作用。

Modulation of idiotypic and antiidiotypic immunoglobulin G responses in an immune thrombocytopenic purpura patient as a consequence of extracorporeal protein A immunoadsorption.

作者信息

Balint J P, Cochran S K, Jones F R

机构信息

IMRE Corporation, Seattle, WA 98109, USA.

出版信息

Artif Organs. 1995 Jun;19(6):496-9. doi: 10.1111/j.1525-1594.1995.tb02368.x.

Abstract

Immune thrombocytopenic purpura (ITP) is an autoimmune disorder characterized by the presence of antiplatelet antibody which sensitizes platelets resulting in their clearance by the reticuloendothelial system. Extracorporeal protein A immunoadsorption has been demonstrated to be of benefit in the treatment of this autoimmune disorder. In the present study, a patient with underlying systemic lupus erythematosus (SLE) presented with ITP. The patient received 14 immunoadsorption treatments and responded to therapy. During the course of immunoadsorption treatments, there was a decline in circulating immune complex (CIC) levels, antinuclear antibody (ANA) levels, and antiplatelet IgG antibody levels. In addition, elevated levels of antiidiotypic IgG antibody detected before initiation of therapy were significantly reduced during the course of immunoadsorption treatments. This study suggests that specific autoimmune idiotypic IgG antibody and corresponding antiidiotypic IgG antibody responses may be modulated in association with extracorporeal immunoadsorption employing protein A/silica columns.

摘要

免疫性血小板减少性紫癜(ITP)是一种自身免疫性疾病,其特征是存在抗血小板抗体,该抗体使血小板致敏,导致其被网状内皮系统清除。体外蛋白A免疫吸附已被证明对治疗这种自身免疫性疾病有益。在本研究中,一名患有潜在系统性红斑狼疮(SLE)的患者出现了ITP。该患者接受了14次免疫吸附治疗,并对治疗有反应。在免疫吸附治疗过程中,循环免疫复合物(CIC)水平、抗核抗体(ANA)水平和抗血小板IgG抗体水平均有所下降。此外,治疗开始前检测到的抗独特型IgG抗体水平在免疫吸附治疗过程中显著降低。这项研究表明,采用蛋白A/硅胶柱的体外免疫吸附可能会调节特定的自身免疫独特型IgG抗体和相应的抗独特型IgG抗体反应。

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