scholarly journals THU0009 ASSOCIATIONS BETWEEN CYTOKINE LEVELS AND TH17/TREG IMMUNE BALANCE IN PATIENTS WITH BEHCET’S DISEASE

Author(s):  
Yue Liu ◽  
Yan Yang ◽  
Rui Su ◽  
Xinyu Zheng ◽  
LI Xiaofeng ◽  
...  
2017 ◽  
Vol 2017 ◽  
pp. 1-13 ◽  
Author(s):  
Bunsoon Choi ◽  
Chang-Hee Suh ◽  
Hyoun-Ah Kim ◽  
Hasan M. Sayeed ◽  
Seonghyang Sohn

The purpose of this study was to clarify the role of pattern recognition receptors in Behçet’s disease (BD). The frequencies of several pattern recognition receptors (CD11b, CD11c, CD32, CD206, CD209, and dectin-1) were analyzed in patients with BD by flow cytometry, and cytokine levels, interleukin- (IL-) 18, IL-23, and IL-17A, were compared in plasma. The analysis was performed in active (n=13) and inactive (n=13) stages of BD patients. Rheumatoid arthritis patients (n=19), as a disease control, and healthy control (HC) (n=19) were enrolled. The frequencies of CD11b+ and CD32+ cells were significantly increased in active BD patients compared to HC. Disease severity score was correlated to CD11c+, CD206+, and CD209+ in whole leukocytes and CD11b+, CD11c+, CD206+, CD209+, and Dectin-1+ in granulocytes. The plasma levels of IL-17A were significantly different between HC and active BD. IL-18 showed significant difference between active and inactive BD patients. From this study, we concluded the expressions of several pattern recognition receptors were correlated to the joint symptoms of BD.


2014 ◽  
Vol 29 (4) ◽  
pp. 317-320 ◽  
Author(s):  
Zeynep Meltem Akkurt ◽  
Mehtap Bozkurt ◽  
Derya Uçmak ◽  
Hatice Yüksel ◽  
Haydar Uçak ◽  
...  

2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 687-688
Author(s):  
Y. Liu ◽  
R. Su ◽  
X. Zheng ◽  
X. LI ◽  
C. Wang

Background:Behcet’s disease(BD) is a systemic perivasculitis where mucocutaneous manifestations are well known to show neutrophilic dermatosis denoted by significant neutrophil infiltration[1]. The neutrophil-to-lymphocyte ratio has been proved as an inflammatory biomarkers in BD[2].At present, the Th17/Treg immune imbalance may be the involved factors in the pathway of BD[3].However, the correlations between the number of neutrophil, the number of lymphocyte, the neutrophil-to-lymphocyte ratio(NLR) and Th17/Treg immune imbalance remain unclear.Objectives:The aim of this study was to examine correlations between the number of neutrophil, the number of lymphocyte, the neutrophil-to-lymphocyte ratio and Th17/Treg immune balance in patients with BD.Methods:The study included 59 BD patients and 66 healthy controls. The absolute counts of lymphocyte subsets and CD4+T cell subsets were detected by flow cytometry for all participants. The neutrophil and lymphocyte were measured by routine blood test for all BD patients. To calculate the NLR, the ratio of absolute neutrophil count to absolute lymphocyte count was obtained. The Mann–Whitney U test was used to compare continuous measures. Correlations between the number of neutrophil, the number of lymphocyte, the NLR and Th17/Treg immune balance were assessed by Spearman’s rank correlation tests.Results:(1)Compared to healthy controls, the absolute counts of NK cells were decreased (P=0.047), the absolute counts of B cells were increased(P=0.021), the absolute counts of CD4+T cells were also increased(P=0.035), the absolute counts of Th1 and Th17 cells were significantly increased(P< 0.005), the absolute counts of Th2 and Treg cells were decreased (P< 0.05), the ratio of Th1/Th2 and Th17/Treg were increased(P< 0.001) in BD group. (2)The numbers of neutrophil were positively correlated with Th17/Treg(r=0.344,P=0.008); The NLR was positively correlated with Th17/Treg(r=0.291,P=0.026).Conclusion:Our research shows that T cell homeostasis perturbation, especially Th17 expansion, Treg insufficiency and Th17/Treg immune imbalance, is the cornerstone of BD pathogenesis. Except neutrophil, these findings suggest that imbalance Th17/Treg may be dominant in the pathogenesis of BD. The NLR was positively correlated with Th17/Treg.Further studies are required to evaluate these preliminary findings in different patient populations and also examine the possible molecular mechanisms behind our observations.References:[1]Tong B, Liu X, Xiao J et al. Immunopathogenesis of Behcet’s Disease[J]. Front Immunol,2019,10:665.DOI:10.3389/fimmu.2019.00665.[2]Gheita TA, Sakr BR, Rabea RE et al. Value of hematological indices versus VEGF as biomarkers of activity in Behçet’s disease[J]. Clin Rheumatol. 2019,38(8):2201–2210. DOI:10.1007/s10067-019-04513-5.[3]Ahmadi M, Yousefi M, Abbaspour-Aghdam S et al. Disturbed Th17/Treg balance, cytokines, and miRNAs in peripheral blood of patients with Behcet’s disease[J]. J Cell Physiol, 2018,234(4):3985-3994.DOI:10.1002/jcp.27207.Figure 1.The absolute counts of lymphocyte subsets in BD patients and healthy controls. Data are expressed as means ±SD.Figure 2.Correlation coefficient and regression line of the number of Th17 cells, the number of Treg cells, Th17/Treg with the the number of neutrophil, the number of lymphocyte, the NLR were represented as scatter plots.Disclosure of Interests:None declared


1991 ◽  
Vol 66 (03) ◽  
pp. 292-294 ◽  
Author(s):  
K K Hampton ◽  
M A Chamberlain ◽  
D K Menon ◽  
J A Davies

SummaryCoagulation and fibrinolytic activities were studied in 18 subjects with Behçet's disease and compared with results from 14 matched control patients suffering from sero-negative arthritis. Significantly higher plasma concentrations (median and range) were found in Behçet's patients for the following variables: fibrinogen 3.7 (1.7-6.9) vs 3.0 (2.0-5.1) g/1, p <0.05; von Willebrand factor antigen, 115 (72-344) vs 74 (60-119)%, p <0.002; plasminogen activator activity (106/ECLT2) 219 (94-329) vs 137 (78-197) units, p <0.002; tissue plasminogen activator inhibitor (t-PA-I) activity, 9.1 (5.5-19.3) vs 5.1 (1.8-12.0) IU/ml, p <0.002; and PAI-1 antigen, 13.9 (4.5-20.9) vs 6.4 (2.4-11.1) ng/ml, p <0.002. Protein C antigen was significantly lower: 97 (70-183) vs 126 (96-220)%, p <0.02. No differences were observed in antithrombin III activity or antigen, factor VIII coagulant activity, fibrinopeptides A and Bβ15-42, plasminogen, α-2-antiplasmin, functional and immunological tissue-plasminogen activator, thrombin-antithrombin complexes and D-dimer. Levels of tissue plasminogen activator inhibitor (activity and antigen) correlated with disease activity while fibrinogen and von Willebrand factor concentrations did not. Seven of the 18 subjects with Behçet's disease had suffered thrombotic events but it was not possible to distinguish these from the 11 patients without thrombosis using the assays performed. The results suggest the abnormal fibrinolytic activity in Behçet's disease is due to increased inhibition of tissue plasminogen activator. No abnormality of coagulation or fibrinolytic activity specific to Behçet's disease was detected.


1996 ◽  
Vol 75 (06) ◽  
pp. 974-975 ◽  
Author(s):  
İbrahim C Haznedaroğlu ◽  
Oktay Özdemir ◽  
Osman Özcebe ◽  
Semra V Dündar ◽  
Şerafettin Kirazli

1993 ◽  
Vol 29 (1) ◽  
pp. 62 ◽  
Author(s):  
Kyung Hwan Lee ◽  
Jae Hyung Park ◽  
Joon Ku Han ◽  
Hyun Ae Park ◽  
Jin Wook Chung ◽  
...  

2018 ◽  
Author(s):  
Ferreira Paulo Carvalho ◽  
Bruno Maia ◽  
Antonio Marinho ◽  
Ana Veloso ◽  
Ivo Cunha ◽  
...  

2002 ◽  
Vol 9 (5) ◽  
pp. 694-698 ◽  
Author(s):  
Silvia B. Gretener ◽  
Dai-Do Do ◽  
Iris Baumgartner ◽  
Hans-Peter Dinkel ◽  
Jürg Schmidli ◽  
...  

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