Markedly Elevated Serum Level of T-Helper Cell 17-Related Cytokines/Chemokines in Acute Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis.
Markedly Elevated Serum Level of T-Helper Cell 17-Related Cytokines/Chemokines in Acute Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis.
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急性髓鞘少突胶质细胞糖蛋白抗体相关视神经炎中 T 辅助细胞 17 相关细胞因子/趋化因子的血清水平显着升高
DOI:
10.3389/fneur.2020.589288
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发表时间:
2020
影响因子:
3.4
通讯作者:
Wei S
中科院分区:
文献类型:
--
作者:
Kang H;Li H;Ai N;Liu H;Xu Q;Tao Y;Wei S
Purpose: The purpose of this study was to examine the differences in immunopathogenesis based on the cytokine/chemokine profiles in myelin oligodendrocyte glycoprotein antibody (MOG-IgG)-positive and -negative groups. Methods: We measured the levels of T-helper cell 17 (Th17) cell-related cytokines/chemokines in 74 serum samples, which were divided into four groups: healthy control (HC) group (n = 15), idiopathic demyelinating optic neuritis (IDON) group (n = 20), aquaporin 4 (AQP4)-IgG-positive optic neuritis (ON) group (n = 18), and MOG-IgG positive-ON group (n = 21). Serum IL17, IL21, IL28, IL31, CXCL1, CXCL2, CCL2, CCL11, CCL20, and LT-α were detected. Results: The serum of the MOG-IgG-positive ON patients showed an obvious elevation of Th17 cell-related cytokines/chemokines compared with that of all the MOG-IgG-negative ON patients. Serum IL17 and IL21 were significantly higher in the ON patients with MOG-IgG positive than in all the other three groups. The serum levels of IL28, IL31, CXCL1, and CCL11 were higher in the ON patients with MOG-IgG positive than in the HC group and the IDON group. The serum concentration of CCL2, CXCL2, and CCL20 in the MOG-IgG-positive and AQP4-IgG-positive group is higher than that of the HC group. No difference in serum LT-α level was found among the four groups. Adjusted multiple regression analyses showed a positive association of IL17 and IL21 levels with the serum concentration of MOG-IgG in the ON patients. Conclusion: The elevated serum level of Th17 cell-related cytokine/chemokines may play an important role in the pathogenesis of MOG-IgG-positive demyelinating ON.
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影响因子:
6.4
作者:
Jarius, Sven;Wildemann, Brigitte
通讯作者:
Wildemann, Brigitte
影响因子:
4.4
作者:
Lindsey, J. W.;Meulmester, K. M.;Wolinsky, J. S.
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Wolinsky, J. S.
影响因子:
30.5
作者:
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通讯作者:
Sallusto, Federica
影响因子:
12.8
作者:
Knier, Benjamin;Rothhammer, Veit;Korn, Thomas
通讯作者:
Korn, Thomas
影响因子:
4.8
作者:
Huppert, Jula;Closhen, Dorothea;Kuhlmann, Christoph R. W.
通讯作者:
Kuhlmann, Christoph R. W.