Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
China National Clinical Research Center for Neurological Diseases, Beijing, China.
Front Immunol. 2021 Jul 16;12:645277. doi: 10.3389/fimmu.2021.645277. eCollection 2021.
Circulating T helper cells with a type 17-polarized phenotype (TH17) and expansion of aquaporin-4 (AQP4)-specific T cells are frequently observed in patients with neuromyelitis optica spectrum disorder (NMOSD). However, naive T cell populations, which give rise to T helper cells, and the primary site of T cell maturation, namely the thymus, have not been studied in these patients. Here, we report the alterations of naive CD4 T cell homeostasis and the changes in thymic characteristics in NMOSD patients. Flow cytometry was performed to investigate the naive CD4 T cell subpopulations in 44 NMOSD patients and 21 healthy controls (HC). On immunological evaluation, NMOSD patients exhibited increased counts of CD31 naive CD4 T cells and CD31 naive CD4 T cells along with significantly higher fraction and absolute counts of peripheral blood CD45RA CD62L naive CD4 T cells. Chest computed tomography (CT) images of 60 NMOSD patients and 65 HCs were retrospectively reviewed to characterize the thymus in NMOSD. Thymus gland of NMOSD patients exhibited unique morphological characteristics with respect to size, shape, and density. NMOSD patients showed exacerbated age-dependent thymus involution than HC, which showed a significant association with disease duration. These findings broaden our understanding of the immunological mechanisms that drive severe disease in NMOSD.
循环中的辅助性 T 细胞具有 17 型极化表型(TH17),水通道蛋白 4(AQP4)特异性 T 细胞扩增,在视神经脊髓炎谱系障碍(NMOSD)患者中经常观察到。然而,在这些患者中,尚未研究产生辅助性 T 细胞的初始 T 细胞群体和 T 细胞成熟的主要部位,即胸腺。在这里,我们报告了 NMOSD 患者中初始 CD4 T 细胞稳态的改变和胸腺特征的变化。通过流式细胞术对 44 名 NMOSD 患者和 21 名健康对照者(HC)的初始 CD4 T 细胞亚群进行了研究。在免疫评估中,NMOSD 患者的 CD31 初始 CD4 T 细胞计数增加,CD31 初始 CD4 T 细胞与外周血 CD45RA CD62L 初始 CD4 T 细胞的分数和绝对计数明显升高。对 60 名 NMOSD 患者和 65 名 HC 的胸部计算机断层扫描(CT)图像进行了回顾性分析,以描述 NMOSD 中的胸腺。NMOSD 患者的胸腺在大小、形状和密度方面表现出独特的形态特征。NMOSD 患者表现出比 HC 更严重的年龄依赖性胸腺萎缩,这与疾病持续时间有显著关联。这些发现拓宽了我们对驱动 NMOSD 严重疾病的免疫机制的理解。