CEDOC, Chronic Diseases Research Center, Immunology, NOVA Medical School | FCM, Universidade Nova de Lisboa, Campo dos Mártires da Pátria, 130, 1169-056, Lisbon, Portugal.
Comprehensive Health Research Centre (CHRC), NOVA Medical School / FCM, Universidade Nova de Lisboa, Lisbon, Portugal.
Clin Rheumatol. 2021 Jul;40(7):2791-2804. doi: 10.1007/s10067-020-05537-y. Epub 2021 Jan 14.
Sjögren's syndrome (SjS) patients exhibit great phenotypical heterogeneity, reinforced by the positiveness of anti-SSA antibody. We aimed to evaluate lymphocyte subpopulations in SSA-positive (SSA+SjS) and SSA-negative (SSA-SjS) SjS patients, Sicca patients, and healthy controls (HC), and to investigate associations between lymphocyte subpopulations and disease activity in SjS.
According to the fulfilment of the ACR/EULAR 2016 classification criteria, patients were included as SjS or as Sicca. HC were selected from the Ophthalmology outpatient clinic. Lymphocyte subpopulations were characterized by flow cytometry. Statistical analysis was performed with GraphPad Prism, with statistical significance concluded if p < 0.05.
We included 53 SjS patients (38 SSA+ and 15 SSA-), 72 Sicca, and 24 HC. SSA+SjS patients presented increased IL-21CD4 and CD8 T cells compared to Sicca and HC, whereas compared to SSA-SjS patients, only IL-21CD4 T cell percentages were increased and Tfh17 percentages and numbers were decreased. Compared to Sicca and HC, SSA+SjS patients had higher levels of CD24CD38 B cells, naïve B cells, and IgMCD38 plasmablasts, and lower levels of memory B cells, including CD24CD27 B cells. SSA+SjS patients with clinically active disease had positive correlations between ESSDAI and IL-21CD4 (p = 0.038, r = 0.456) and IL-21CD8 T cells (p = 0.046, r = 0.451).
In SjS, a distinct lymphocyte subset distribution profile seems to be associated with positive anti-SSA. Moreover, the association between ESSDAI and IL-21CD4 and IL-21CD8 (follicular) T cells in SSA+SjS patients suggests the involvement of these cells in disease pathogenesis and activity, and possibly their utility for the prognosis and assessment of response to therapy. Key Points • SSA+SjS patients have a pronounced naïve/memory B cell imbalance. • SSA+SjS patients have more active disease associated with IL-21CD4 and IL-21CD8 follicular T cell expansion. • IL-21CD4 and IL-21CD8 T cell quantification may be useful for the prognosis and assessment of response to therapy.
干燥综合征(SjS)患者表现出很大的表型异质性,抗 SSA 抗体呈阳性进一步证实了这一点。我们旨在评估 SSA 阳性(SSA+SjS)和 SSA 阴性(SSA-SjS)SjS 患者、干燥症患者和健康对照者(HC)中的淋巴细胞亚群,并探讨 SjS 中淋巴细胞亚群与疾病活动度之间的关系。
根据 ACR/EULAR 2016 分类标准,将患者纳入 SjS 或干燥症。HC 从眼科门诊选择。通过流式细胞术对淋巴细胞亚群进行特征分析。采用 GraphPad Prism 进行统计分析,如果 p<0.05,则认为具有统计学意义。
我们纳入了 53 例 SjS 患者(38 例 SSA+和 15 例 SSA-)、72 例干燥症患者和 24 例 HC。与干燥症和 HC 相比,SSA+SjS 患者的 IL-21CD4 和 CD8 T 细胞增加,而与 SSA-SjS 患者相比,仅 IL-21CD4 T 细胞百分比增加,Tfh17 百分比和数量减少。与干燥症和 HC 相比,SSA+SjS 患者的 CD24CD38 B 细胞、幼稚 B 细胞和 IgMCD38 浆母细胞水平更高,记忆 B 细胞(包括 CD24CD27 B 细胞)水平更低。临床活动期的 SSA+SjS 患者的 ESSDAI 与 IL-21CD4(p=0.038,r=0.456)和 IL-21CD8 T 细胞(p=0.046,r=0.451)呈正相关。
在 SjS 中,与抗 SSA 阳性相关的似乎是独特的淋巴细胞亚群分布特征。此外,SSA+SjS 患者的 ESSDAI 与 IL-21CD4 和 IL-21CD8(滤泡)T 细胞之间的相关性表明这些细胞参与了疾病的发病机制和活动,并且可能对预后和治疗反应的评估有用。
SSA+SjS 患者存在明显的幼稚/记忆 B 细胞失衡。
SSA+SjS 患者疾病更活跃,与 IL-21CD4 和 IL-21CD8 滤泡 T 细胞扩增相关。
IL-21CD4 和 IL-21CD8 T 细胞的定量检测可能对预后和治疗反应的评估有用。