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局限性硬皮病和泛发性硬皮病中的抗核抗体和抗单链DNA抗体。

Antinuclear and anti-single-stranded DNA antibodies in morphea and generalized morphea.

作者信息

Falanga V, Medsger T A, Reichlin M

出版信息

Arch Dermatol. 1987 Mar;123(3):350-3.

PMID:3545090
Abstract

The clinical features of localized scleroderma have allowed investigators to distinguish three morphologic variants: morphea, generalized morphea, and linear scleroderma. The latter has been reported to have a higher frequency of antinuclear antibodies and has been associated with antibodies to single-stranded DNA (ssDNA). In this study we determined the frequency of antinuclear antibodies and anti-ssDNA antibodies in 22 patients with morphea or generalized morphea. None had Raynaud's phenomenon or evidence of a systemic connective-tissue disease. Antinuclear antibodies were present in 18% of patients when serum samples were tested on mouse kidney substrate but were found in 50% of HEp-2 cells. The serum samples contained anti-ssDNA antibodies in 59% of the patients, with the highest levels of ssDNA binding observed in patients with generalized morphea. The frequency of antibodies to ssDNA was higher in patients with clinical evidence of active compared with inactive disease. Discordance in immune reactivity indicates that at least three distinctive serum autoantibodies exist in morphea and generalized morphea: anti-ssDNA antibodies and antinuclear antibodies with either homogeneous or speckled immunofluorescence patterns. These findings are similar to those recently described in linear scleroderma and suggest that comparable serum autoantibody abnormalities are present in all the variants of localized scleroderma.

摘要

局限性硬皮病的临床特征使研究者能够区分出三种形态学变体

硬斑病、泛发性硬斑病和线状硬皮病。据报道,后者抗核抗体的出现频率较高,且与抗单链DNA(ssDNA)抗体有关。在本研究中,我们测定了22例硬斑病或泛发性硬斑病患者抗核抗体和抗ssDNA抗体的出现频率。所有患者均无雷诺现象或系统性结缔组织病的证据。当血清样本在小鼠肾底物上检测时,18%的患者存在抗核抗体,但在HEp-2细胞检测中,这一比例为50%。59%的患者血清样本含有抗ssDNA抗体,其中泛发性硬斑病患者的ssDNA结合水平最高。与疾病无活动迹象的患者相比,有活动迹象的患者抗ssDNA抗体的出现频率更高。免疫反应性的不一致表明,硬斑病和泛发性硬斑病中至少存在三种不同的血清自身抗体:抗ssDNA抗体以及具有均质或斑点状免疫荧光模式的抗核抗体。这些发现与最近在线状硬皮病中描述的结果相似,提示局限性硬皮病的所有变体中均存在类似的血清自身抗体异常。

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