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首页> 外文期刊>Journal of Thoracic Disease >CD31 + , CD38 + , CD44 + , and CD103 + lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls
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CD31 + , CD38 + , CD44 + , and CD103 + lymphocytes in peripheral blood, bronchoalveolar lavage fluid and lung biopsy tissue in sarcoid patients and controls

机译:CD31 +,CD38 +,CD44 +和CD103 +淋巴细胞在外周血,支气管肺泡灌洗液和肺活检组织在术语患者和对照中

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Background: The mechanisms driving the transition from inflammation to fibrosis in sarcoidosis patients are poorly understood; prognostic features are lacking. Immune cell profiling may provide insights into pathogenesis and prognostic factors of the disease. This study aimed to establish associations in simultaneous of lymphocyte subset profiles in the blood, bronchoalveolar lavage fluid (BALF), and lung biopsy tissue in the patients with newly diagnosed sarcoidosis. Methods: A total of 71 sarcoid patients (SPs) and 20 healthy controls (HCs) were enrolled into the study. CD31, CD38, CD44, CD103 positive T lymphocytes in blood and BALF were analysed. Additionally, the densities of CD4, CD8, CD38, CD44, CD103 positive cells in lung tissue biopsies were estimated by digital image analysis. Results: Main findings: (I) increase of percentage of CD3 + CD4 + CD38 + in BALF and blood, and increase of percentage of CD3 + CD4 + CD44 + in BALF in L?fgren syndrome patients comparing with patients without L?fgren syndrome, (II) increase of percentage of CD3 + CD4 + 103 + in BALF and in blood in patients without L?fgren syndrome (comparing with L?fgren syndrome patients) and increase of percentage of CD3 + CD4 + 103 + in BALF and in blood in more advanced sarcoidosis stage. (III) Increasing percentage of BALF CD3 + CD4 + CD31 + in sarcoidosis patients when comparing with controls independently of presence of L?fgren syndrome, smoking status or stage of sarcoidosis. Several significant correlations were found. Conclusions: Lymphocyte subpopulations in blood, BALF, and lung tissue were substantially different in SPs at the time of diagnosis compared to HCs. CD3 + CD4 + CD31 + in BALF might be a potential supporting marker for the diagnosis of sarcoidosis. CD3 + CD4 + CD38 + in BALF and blood and CD3 + CD4 + CD44 + in BALF may be markers of the acute immune response in sarcoidosis patients. CD4 + CD103 + T-cells in BALF and in blood are markers of the persistent immune response in sarcoidosis patients and are potential prognostic features of the chronic course of this disease.
机译:背景:驱动从炎症到结节病患者纤维化的过渡的机制很差;缺乏预后特征。免疫细胞分析可以为疾病的发病和预后因子提供洞察。本研究旨在建立新诊断的结节病患者血液,支气管肺泡灌洗液(BALF)和肺活检组织中同时患有淋巴细胞子集谱的关联。方法:共纳入研究中,共有71名SARARIOD患者(SPS)和20例健康对照(HCS)。分析CD31,CD38,CD44,CD103血液和BALF阳性T淋巴细胞。另外,通过数字图像分析估计了肺组织活检中CD4,CD8,CD38,CD44,CD103阳性细胞的密度。结果:主要发现:(i)在L的BALF和血液中的CD3 + CD4 + CD38 +的百分比增加,以及L的BALF中的CD3 + CD4 + CD44 +的百分比增加与没有L的患者的患者(FGREN综合征) (ii)(ii)在没有L的患者中增加了CD3 + CD4 + 103 +的百分比,没有L?FGREN综合征(与L?FGREN综合征患者相比),并在BALF和BALF中的CD3 + CD4 + 103 +的百分比增加血液中更先进的顺序病变。 (iii)与单独存在L?FGREN综合征,吸烟状态或结节病的阶段的对照相比,在与对照组织相比,患者百分比的百叶菌CD3 + CD4 + CD31 +百分比增加。发现了几种显着的相关性。结论:与HCS相比,血液,BALF和肺组织中的淋巴细胞群在SPS中基本上不同。 BALF中的CD3 + CD4 + CD31 +可能是诊断结节病的潜在支持标志物。 BALF和血液中CD3 + CD4 + CD38 + BALF中的CD3 + CD4 + CD44 +可能是结节病患者急性免疫应答的标志物。 BALF和血液中的CD4 + CD103 + T细胞是结节病症患者持续免疫应答的标志物,并且是这种疾病慢性过程的潜在预后特征。

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