Iwase O, Aoki I, Kuriyama Y, Uchida Y, Aizawa S, Nakano M, Toyama K
First Department of Internal Medicine, Tokyo Medical College.
Rinsho Ketsueki. 1995 Jan;36(1):1-5.
To clarify a role of immunoregulatory T cells in the pathophysiology of autoimmune hemolytic anemia (AIHA), we investigated T cell subsets in the peripheral blood of 15 patients with AIHA by two color analysis using flow cytometry. Consequently both CD4+ cells and CD4+CD45RA+ cells decreased in proportion, irrespective of the disease activity (active or remission phase). CD4+CD45RA+ cells are regarded as naive T cells. Incidentally the ratio of CD45RA+ cells in CD4+ cells also fell in the low level in active phase, but it recovered to the normal ratio in remission. On the other hand, CD8+ cells and CD8+ +S6F1+ cells that may represent activated cytotoxic T lymphocytes increased in active phase and then both entered the normal range in remission. These findings suggest that AIHA could be caused partly by the alternative balance of CD4+CD45RA+ cells probably constituting a member of IRT and moreover by the activation of CTL.
为阐明免疫调节性T细胞在自身免疫性溶血性贫血(AIHA)病理生理学中的作用,我们通过流式细胞术双色分析研究了15例AIHA患者外周血中的T细胞亚群。结果显示,无论疾病活动状态(活动期或缓解期)如何,CD4+细胞和CD4+CD45RA+细胞的比例均下降。CD4+CD45RA+细胞被视为初始T细胞。顺便提一下,活动期CD4+细胞中CD45RA+细胞的比例也降至低水平,但在缓解期恢复到正常比例。另一方面,可能代表活化细胞毒性T淋巴细胞的CD8+细胞和CD8+S6F1+细胞在活动期增加,然后在缓解期均进入正常范围。这些发现表明,AIHA可能部分是由可能构成免疫调节性T细胞(IRT)成员之一的CD4+CD45RA+细胞的交替平衡引起的,此外还由细胞毒性T淋巴细胞(CTL)的激活引起。