Yu Hong, Zhang Jiangbo, Fu Rong, Liu Hui, Wang Huaquan, Ding Kai, Wang Yihao, Li Lijuan, Wang Honglei, Shao Zonghong
Department of Hematology, Tianjin Medical University General Hospital, 154 Anshan Street, Heping District, Tianjin 300052, China.
Clin Dev Immunol. 2013;2013:730450. doi: 10.1155/2013/730450. Epub 2013 Aug 27.
Immune-related pancytopenia (IRP) is one kind of bone marrow failure diseases which is related to autoantibodies. Autoantibodies have been detected on the membrane of various bone marrow (BM) hemopoietic cells by BM mononuclear-cell-Coombs test or flow cytometric analysis. There are autoantibodies in the BM supernatant of IRP patients, which can target several antigens on hematopoietic cells membranes by western blot. T follicular helper (Tfh) cells are the true helper cells for Ab responses, which represent one of the most numerous and important subsets of effector T cells. Dysregulation of Tfh cell function or expression of Tfh cell-associated molecules could contribute to the pathogenesis of autoimmune diseases. Currently, there are no studies regarding the role of Tfh cells in IRP patients. The percentages of Tfh cells, Tfh-related molecules ICOS, CD40L, IL-21, and Bcl-6 in BM were investigated in 90 patients with IRP, and 25 healthy controls. We observed that there exist increased quantity and hyperfunction of Tfh cells in IRP, and the results were correlated with patient characteristics. It was indicated that dysregulated Tfh cells might be involved in the pathogenesis of IRP and that inhibition of Tfh cells effector molecules might provide opportunities for new therapeutic approaches to IRP and even other human autoimmune diseases.
免疫相关性全血细胞减少症(IRP)是一种与自身抗体相关的骨髓衰竭性疾病。通过骨髓单个核细胞抗人球蛋白试验或流式细胞术分析,已在各种骨髓造血细胞表面检测到自身抗体。IRP患者的骨髓上清液中存在自身抗体,通过蛋白质印迹法可发现其能靶向造血细胞膜上的多种抗原。滤泡辅助性T(Tfh)细胞是抗体应答的真正辅助细胞,是效应T细胞中数量最多且最重要的亚群之一。Tfh细胞功能失调或Tfh细胞相关分子表达异常可能导致自身免疫性疾病的发病机制。目前,尚无关于Tfh细胞在IRP患者中作用的研究。我们对90例IRP患者和25名健康对照者的骨髓中Tfh细胞、Tfh相关分子诱导性共刺激分子(ICOS)、CD40配体(CD40L)、白细胞介素-21(IL-21)和Bcl-6的百分比进行了研究。我们观察到IRP患者中Tfh细胞数量增加且功能亢进,结果与患者特征相关。这表明失调的Tfh细胞可能参与了IRP的发病机制,抑制Tfh细胞效应分子可能为IRP乃至其他人类自身免疫性疾病提供新的治疗途径。