Sakai H, Miyazaki M, Endoh M, Nomoto Y
Department of Internal Medicine, School of Medicine, Tokai University, Isehara City, Japan.
Clin Exp Immunol. 1989 Dec;78(3):378-82.
Enumeration and functional analysis of CD4+ T cells with receptors for the Fc portion of IgA (i.e. T alpha 4 cells) in the peripheral blood of patients with IgA nephropathy, their relatives and age-matched controls were performed to elucidate polyclonal activation of IgA production in this disease. Enumeration of T alpha 4 cells was performed by a fluorescence activated cell sorter, and functional analysis was carried out by separation of T alpha 4 cells, and IgM-, IgA- and IgG-bearing lymphocytes using panning methods followed by cultures of these cells for 7 days with pokeweed mitogen. There was a significant increase in the amount of peripheral blood T alpha 4 cells in patients with IgA nephropathy and their relatives. T alpha 4 cells specifically enhanced the switch of IgM-bearing cells to IgA-bearing cells, and this switch activity was inhibited by addition of human myeloma IgA. It is suggested that T alpha 4 cells may be responsible for polyclonal activation of IgA production in IgA nephropathy.
对IgA肾病患者、其亲属及年龄匹配的对照者外周血中具有IgA Fc段受体的CD4⁺ T细胞(即Tα4细胞)进行计数和功能分析,以阐明该疾病中IgA产生的多克隆激活情况。Tα4细胞的计数通过荧光激活细胞分选仪进行,功能分析则是通过使用淘选法分离Tα4细胞以及携带IgM、IgA和IgG的淋巴细胞,随后将这些细胞与商陆有丝分裂原一起培养7天。IgA肾病患者及其亲属外周血Tα4细胞数量显著增加。Tα4细胞特异性增强了携带IgM的细胞向携带IgA的细胞的转换,并且这种转换活性会因加入人骨髓瘤IgA而受到抑制。提示Tα4细胞可能是IgA肾病中IgA产生多克隆激活的原因。