Xin Li, Shengxiao Zhang, Ting Cheng, Jia Wang, Fang Li, Lei Shi, Xiaofeng Li
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The clinical data were gathered, and cytokines and peripheral blood lymphocyte subsets were quantified using flow cytometry and the Cytometric Bead Array (CBA), respectively.</p><p><strong>Results: </strong>Patients with pSS-HI were more likely than those without pSS-HI to develop skin involvement, had a higher positive rate of anti-SSA antibody, and had elevated levels of IgA, IgG, and ESR. Compared to the pSS-non-HI group, the number of all lymphocyte subsets was lower in the pSS-HI group. However, the proportion of Th2 cells in the pSS-HI group was higher than those in the pSS-non-HI group. In contrast to the pSS-non-HI group, the pSS-HI group exhibited elevated levels of IL-10 and decreased levels of IL-4. A significant correlation was observed between IL-10 and the number of total T cells, CD4+ T cells, CD8+ T cells, NK cells, Th1 cells, Th2 cells, and Th17 cells. In the context of pSS-HI, protective factors may include the number of Treg cells and CD4+ T cells, whereas risk factors may include IgA and the number of Th2 cells.</p><p><strong>Conclusions: </strong>An immunological mechanism potentially implicated in the development of pSS-HI may be the elevation of IL-10 and the reduction of peripheral blood CD4+ T cell subsets (particularly Treg cells) and serum IL-4 levels.</p>","PeriodicalId":10274,"journal":{"name":"Clinical and experimental rheumatology","volume":" ","pages":"2412-2419"},"PeriodicalIF":3.4000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The abnormal expression of peripheral blood CD4+ T lymphocyte subsets are correlated with primary Sjögren's syndrome complicated with haematological involvement.\",\"authors\":\"Xin Li, Shengxiao Zhang, Ting Cheng, Jia Wang, Fang Li, Lei Shi, Xiaofeng Li\",\"doi\":\"10.55563/clinexprheumatol/st9u8m\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>Complicated primary Sjögren's syndrome (pSS) with haematological involvement (HI) is not uncommon; however, the aetiology of this condition remains obscure. The clinical characteristics, cytokine levels, and expression of peripheral blood lymphocyte subsets (CD4+ T lymphocyte subsets in particular) of patients with pSS-HI were investigated in this study.</p><p><strong>Methods: </strong>The pSS-HI group (n = 43), the pSS complicated without HI (pSS-non-HI) group (n = 94), and the healthy controls (HCs) group (n = 40) were enrolled in the Second Hospital of Shanxi Medical University. The clinical data were gathered, and cytokines and peripheral blood lymphocyte subsets were quantified using flow cytometry and the Cytometric Bead Array (CBA), respectively.</p><p><strong>Results: </strong>Patients with pSS-HI were more likely than those without pSS-HI to develop skin involvement, had a higher positive rate of anti-SSA antibody, and had elevated levels of IgA, IgG, and ESR. Compared to the pSS-non-HI group, the number of all lymphocyte subsets was lower in the pSS-HI group. 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引用次数: 0
摘要
目的:并发原发性斯约格伦综合征(pSS)并伴有血液学受累(HI)的情况并不少见,但其病因仍不明确。本研究调查了 pSS-HI 患者的临床特征、细胞因子水平和外周血淋巴细胞亚群(尤其是 CD4+ T 淋巴细胞亚群)的表达:山西医科大学第二医院收治的pSS-HI组(43例)、pSS并发无HI(pSS-non-HI)组(94例)和健康对照(HCs)组(40例)。收集临床数据,并分别使用流式细胞术和细胞计数珠阵列(CBA)对细胞因子和外周血淋巴细胞亚群进行定量分析:结果:与非 pSS-HI 患者相比,pSS-HI 患者更容易出现皮肤受累,抗 SSA 抗体阳性率更高,IgA、IgG 和 ESR 水平升高。与 pSS 非 HI 组相比,pSS-HI 组所有淋巴细胞亚群的数量均较低。然而,pSS-HI 组 Th2 细胞的比例高于 pSS 非 HI 组。与 pSS 非 HI 组相比,pSS-HI 组的 IL-10 水平升高,IL-4 水平降低。IL-10与T细胞总数、CD4+ T细胞、CD8+ T细胞、NK细胞、Th1细胞、Th2细胞和Th17细胞数量之间存在明显的相关性。就 pSS-HI 而言,保护因素可能包括 Treg 细胞和 CD4+ T 细胞的数量,而风险因素可能包括 IgA 和 Th2 细胞的数量:结论:可能与 pSS-HI 发病有关的免疫机制可能是 IL-10 升高、外周血 CD4+ T 细胞亚群(尤其是 Treg 细胞)和血清 IL-4 水平降低。
The abnormal expression of peripheral blood CD4+ T lymphocyte subsets are correlated with primary Sjögren's syndrome complicated with haematological involvement.
Objectives: Complicated primary Sjögren's syndrome (pSS) with haematological involvement (HI) is not uncommon; however, the aetiology of this condition remains obscure. The clinical characteristics, cytokine levels, and expression of peripheral blood lymphocyte subsets (CD4+ T lymphocyte subsets in particular) of patients with pSS-HI were investigated in this study.
Methods: The pSS-HI group (n = 43), the pSS complicated without HI (pSS-non-HI) group (n = 94), and the healthy controls (HCs) group (n = 40) were enrolled in the Second Hospital of Shanxi Medical University. The clinical data were gathered, and cytokines and peripheral blood lymphocyte subsets were quantified using flow cytometry and the Cytometric Bead Array (CBA), respectively.
Results: Patients with pSS-HI were more likely than those without pSS-HI to develop skin involvement, had a higher positive rate of anti-SSA antibody, and had elevated levels of IgA, IgG, and ESR. Compared to the pSS-non-HI group, the number of all lymphocyte subsets was lower in the pSS-HI group. However, the proportion of Th2 cells in the pSS-HI group was higher than those in the pSS-non-HI group. In contrast to the pSS-non-HI group, the pSS-HI group exhibited elevated levels of IL-10 and decreased levels of IL-4. A significant correlation was observed between IL-10 and the number of total T cells, CD4+ T cells, CD8+ T cells, NK cells, Th1 cells, Th2 cells, and Th17 cells. In the context of pSS-HI, protective factors may include the number of Treg cells and CD4+ T cells, whereas risk factors may include IgA and the number of Th2 cells.
Conclusions: An immunological mechanism potentially implicated in the development of pSS-HI may be the elevation of IL-10 and the reduction of peripheral blood CD4+ T cell subsets (particularly Treg cells) and serum IL-4 levels.
期刊介绍:
Clinical and Experimental Rheumatology is a bi-monthly international peer-reviewed journal which has been covering all clinical, experimental and translational aspects of musculoskeletal, arthritic and connective tissue diseases since 1983.