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(新西兰白兔×BXSB)F1小鼠和人类系统性红斑狼疮中抗核仁磷酸蛋白抗体与抗心磷脂抗体之间的关联

Association between anti-nucleophosmin and anti-cardiolipin antibodies in (NZW x BXSB)F1 mice and human systemic lupus erythematosus.

作者信息

Lartigue Aurelia, Drouot Laurent, Jouen Fabienne, Charlionet Roland, Tron François, Gilbert Danièle

机构信息

INSERM U519 and Institut Fédératif de Recherche Multidisciplinaire sur les Peptides, Faculté de Médecine et Pharmacie, 22 boulevard Gambetta, 76183 Rouen Cedex, France.

出版信息

Arthritis Res Ther. 2005;7(6):R1394-403. doi: 10.1186/ar1838. Epub 2005 Oct 13.

Abstract

We showed previously that nucleophosmin (NPM), a nucleolar phosphoprotein, is recognized by sera from (NZW x BXSB)F1 (WB) mice, a model of systemic lupus erythematosus (SLE) and anti-phospholipid syndrome. In the present study we analysed the prevalence and kinetics of anti-NPM autoantibodies in WB mice by a solid-phase ELISA with recombinant human (rh) NPM as the antigen and showed that most male WB mouse sera had anti-NPM antibodies that were responsible for their indirect immunofluorescence staining pattern on Hep-2 cells. Anti-NPM antibodies were significantly associated with anti-cardiolipin (aCL) antibodies. This antibody profile mirrored that observed in certain human SLE sera because anti-NPM antibodies were detected in 28% of the sera from patients with SLE and were similarly associated with aCL antibodies. The demonstration that rhNPM bound to cardiolipin (CL) in vitro and increased the CL-binding activity of a WB-derived aCL monoclonal antibody indicates that NPM can interact with CL to form SLE-related immunogenic particles that might be responsible for the concomitant production of anti-NPM and aCL antibodies.

摘要

我们之前曾表明,核仁磷蛋白(NPM),一种核仁磷蛋白,可被(新西兰白兔×BXSB)F1(WB)小鼠的血清识别,该小鼠是系统性红斑狼疮(SLE)和抗磷脂综合征的模型。在本研究中,我们以重组人(rh)NPM为抗原,通过固相酶联免疫吸附测定(ELISA)分析了WB小鼠中抗NPM自身抗体的患病率和动力学,并表明大多数雄性WB小鼠血清具有抗NPM抗体,这些抗体导致了它们在Hep - 2细胞上的间接免疫荧光染色模式。抗NPM抗体与抗心磷脂(aCL)抗体显著相关。这种抗体谱反映了在某些人类SLE血清中观察到的情况,因为在28%的SLE患者血清中检测到了抗NPM抗体,并且它们同样与aCL抗体相关。体外实验表明rhNPM与心磷脂(CL)结合并增加了WB来源的aCL单克隆抗体的CL结合活性,这表明NPM可以与CL相互作用形成与SLE相关的免疫原性颗粒,这可能是抗NPM和aCL抗体同时产生的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5184/1297587/4ceee33a2c43/ar1838-1.jpg

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