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[韦格纳肉芽肿病与抗中性粒细胞胞浆颗粒自身抗体]

[Wegener's granulomatosis and autoantibodies against cytoplasmic granules of neutrophils].

作者信息

Joller-Jemelka H I, Grob P J

机构信息

Departement für Innere Medizin, Universitätsspital Zürich.

出版信息

Schweiz Med Wochenschr. 1988 Aug 20;118(33):1163-8.

PMID:3175567
Abstract

According to the literature, autoantibodies against extranuclear components of polynuclear granulocytes (ACPA) are almost exclusively present in sera of patients with Wegener's granulomatosis and their serum concentrations reflect disease activity. When measurement of these autoantibodies was introduced in our routine laboratory, 12 out of the first 70 samples gave positive results by enzyme immunoassay and by indirect immunofluorescence on alcohol-fixed granulocytes. The 12 patients with ACPA proved to have Wegener's granulomatosis. The titers were distinctly higher in patients without therapy than in those under an immunosuppressive regimen. As a control, 250 sera were tested of patients with various disorders such as SLE, rheumatoid arthritis, acute and chronic hepatitis etc. ACPA were detected in 4 individuals (1 patient with acute non A/non B hepatitis, 2 patients with chronic aggressive hepatitis and 1 hemodialysis patient with unclear glomerulonephritis). These results further confirm the diagnostic value of ACPA in Wegener's granulomatosis.

摘要

根据文献,抗多核粒细胞核外成分的自身抗体(ACPA)几乎仅存在于韦格纳肉芽肿患者的血清中,其血清浓度反映疾病活动度。当我们常规实验室开始检测这些自身抗体时,最初的70份样本中有12份通过酶免疫测定法以及在酒精固定的粒细胞上进行间接免疫荧光检测得出阳性结果。这12例ACPA阳性患者被证实患有韦格纳肉芽肿。未接受治疗的患者其滴度明显高于接受免疫抑制治疗方案的患者。作为对照,对250例患有各种疾病(如系统性红斑狼疮、类风湿性关节炎、急慢性肝炎等)的患者血清进行了检测。在4例个体中检测到了ACPA(1例急性非甲非乙型肝炎患者、2例慢性侵袭性肝炎患者和1例肾小球肾炎病因不明的血液透析患者)。这些结果进一步证实了ACPA在韦格纳肉芽肿中的诊断价值。

引用本文的文献

1
The current status of neutrophil cytoplasmic antibodies.
Clin Exp Immunol. 1989 Nov;78(2):143-8.
2
Wegener's granulomatosis. Thoughts and observations of a pathologist.
Eur Arch Otorhinolaryngol. 1990;247(3):133-42. doi: 10.1007/BF00175962.

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