淋巴
生发中心
医学
淋巴结
病理
等离子体电池
高丙种球蛋白血症
卡斯特曼病
细胞因子
增生
免疫学
疾病
B细胞
抗体
骨髓
作者
Kazuyuki Yoshizaki,Tadashi Matsuda,Naoki Nishimoto,Taro Kuritani,L Taeho,K Aozasa,Tatsutoshi Nakahata,Hiroshi Kawai,Hiromi Tagoh,Takahiro Komori
出处
期刊:Blood
[Elsevier BV]
日期:1989-09-01
卷期号:74 (4): 1360-1367
被引量:904
标识
DOI:10.1182/blood.v74.4.1360.1360
摘要
Castleman's disease is a syndrome consisting of giant lymph node hyperplasia with plasma cell infiltration, fever, anemia, hypergammaglobulinemia, and an increase in the plasma level of acute phase proteins. It has been reported that clinical abnormalities disappear after the resection of the affected lymph nodes, suggesting that products of lymph nodes may cause such clinical abnormalities. Interleukin-6 (IL-6) is a cytokine inducing B-cell differentiation to immunoglobulin-producing cells and regulating biosynthesis of acute phase proteins. This report demonstrates that the germinal centers of hyperplastic lymph nodes of patients with Castleman's disease produce large quantities of IL-6 without any significant production of other cytokines. In a patient with a solitary hyperplastic lymph node, clinical improvement and decrease in serum IL-6 were observed following surgical removal of the involved lymph node. There was a correlation between serum IL-6 level, lymph node hyperplasia, hypergammaglobulinemia, increased level of acute phase proteins, and clinical abnormalities. The findings in this report indicate that the generation of IL-6 by B cells in germinal centers of hyperplastic lymph nodes of Castleman's disease may be the key element responsible for the variety of clinical symptoms in this disease.
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