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[系统性红斑狼疮和慢性多关节炎中IgG抗体诱导血小板获得性储存池缺陷]

[The induction of an acquired storage pool deficiency of the thrombocytes by IgG antibodies in systemic lupus erythematosus and chronic polyarthritis].

作者信息

Falke S, Avenarius H J, Deicher H

机构信息

Zentrum für Innere Medizin und Dermatologie, Medizinische Hochschule Hannover.

出版信息

Z Rheumatol. 1990 Mar-Apr;49(2):70-6.

PMID:2349839
Abstract

Sera of patients with RA and SLE contain platelet-reactive IgG antibodies, which bring about the release of serotonin from platelets. They can also induce the aggregation of normal human platelets. In addition, such antibodies cause a decreased in vitro disaggregation of platelets after ADP exposure, as well as a significantly reduced collagen-induced aggregation. Thus, IgG platelet antibodies in RA and SLE can cause a functional impairment of patients' platelets, and may also be instrumental in systemic inflammatory rheumatoid disease by releasing proinflammatory mediators.

摘要

类风湿关节炎(RA)和系统性红斑狼疮(SLE)患者的血清中含有血小板反应性IgG抗体,这些抗体可导致血小板释放5-羟色胺。它们还能诱导正常人血小板聚集。此外,此类抗体可使ADP暴露后血小板的体外解聚减少,以及胶原诱导的聚集显著降低。因此,RA和SLE中的IgG血小板抗体可导致患者血小板功能受损,还可能通过释放促炎介质在系统性炎性类风湿疾病中起作用。

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