Increased RP105-Negative B Cells in IgG4-Related Disease.

Q4 Medicine Open Rheumatology Journal Pub Date : 2013-08-23 eCollection Date: 2013-01-01 DOI:10.2174/1874312901307010055
S Koarada, S Tashiro, N Nagao, R Suematsu, A Ohta, Y Tada
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引用次数: 5

Abstract

Four patients with IgG4-related disease (IgG4-RD) showed increased percentages of RP105-negative B cells in the peripheral blood. Case 1: A 66-year-old man having retroperitoneal fibrosis had 18.8% of RP105-negative B cells. Oral prednisolone improved the affected lesions and the percentage of RP105-negative B cells decreased (3.2%) after the treatment. Case 2: A 53-year-old man with retroperitoneal fibrosis had 27.9% of RP105-negative B cells. Case 3: A 38-year-old man with follicular hyperplasia showed increased percentage of RP105-negative B cells (8.3%). Case 4: A 60-year-old man with interstitial nephritis had 27.5% of RP105-negative B cells. The treatment decreased the numbers of RP105-negative B cells. Increased numbers of RP105-negatvie B cells is possibly associated with disease activity of IgG4-RD. Analysis of expression of RP105 on B cells may be helpful in evaluation of disease activity of IgG4-RD.

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igg4相关疾病中rp105阴性B细胞增加。
4例igg4相关疾病(IgG4-RD)患者外周血中rp105阴性B细胞百分比升高。病例1:66岁男性腹膜后纤维化,有18.8% rp105阴性B细胞。口服强的松龙改善了病变,治疗后rp105阴性B细胞百分比下降(3.2%)。病例2:53岁男性腹膜后纤维化患者有27.9%的rp105阴性B细胞。病例3:38岁男性滤泡增生,rp105阴性B细胞比例增加(8.3%)。病例4:60岁间质性肾炎患者有27.5% rp105阴性B细胞。处理后rp105阴性B细胞数量减少。rp105阴性B细胞数量的增加可能与IgG4-RD的疾病活性有关。分析RP105在B细胞上的表达可能有助于评价IgG4-RD的疾病活性。
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来源期刊
Open Rheumatology Journal
Open Rheumatology Journal Medicine-Rheumatology
CiteScore
0.80
自引率
0.00%
发文量
2
期刊介绍: ENTHAM Open publishes a number of peer-reviewed, open access journals. These free-to-view online journals cover all major disciplines of science, medicine, technology and social sciences. BENTHAM Open provides researchers a platform to rapidly publish their research in a good-quality peer-reviewed journal. All peer-reviewed accepted submissions meeting high research and ethical standards are published with free access to all.
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