Inhibition of Inflammatory Cytokines and Induction of Myeloid‐Derived Suppressor Cells by the Effects of Granulocyte and Monocyte Adsorption Apheresis
Inhibition of Inflammatory Cytokines and Induction of Myeloid‐Derived Suppressor Cells by the Effects of Granulocyte and Monocyte Adsorption Apheresis
复制标题
粒细胞和单核细胞吸附分离术对炎症细胞因子的抑制和骨髓源性抑制细胞的诱导
DOI:
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发表时间:
2017
影响因子:
1.9
通讯作者:
T. Kanekura
中科院分区:
文献类型:
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作者:
M. Sakanoue;Y. Higashi;T. Kanekura
Pro‐inflammatory cytokines are involved in the pathogenesis of inflammatory skin diseases attributable to activated neutrophils and macrophages. Myeloid‐derived suppressor cells (MDSCs) play an important role in the regulation of the immune response and possess strong immunosuppressive and anti‐inflammatory properties. Granulocyte and monocyte adsorption apheresis (GMA), an extracorporeal apheresis instrument featuring columns containing cellulose acetate (CA) beads, is designed to remove pathogenic myeloid lineage cells. The purpose of this study was to investigate the effects of GMA on cytokine production and MDSC induction. The serum level of various inflammatory cytokines and the incidence of MDSCs in peripheral blood before and after GMA treatment were recorded. Cytokines were assayed with the suspension‐array method in 38 patients. The incidence of MDSCs was analyzed by FACS in eight patients and the effect of GMA on in vitro MDSC induction was examined using a mini‐column system that mimics GMA. The serum level of IL‐2Rα (P = 0.030), IL‐8 (P = 0.018), and MIF (P = 0.0002) was significantly decreased by GMA and the incidence of MDSCs was increased (P = 0.030). With the mini‐column system, MDSCs were induced in the peripheral blood of five healthy volunteers; the in vitro induction was significantly inhibited by inactivation of the complement component iC3b. The clinical effectiveness of GMA may be attributable to the inhibition of pro‐inflammatory cytokines and the induction of anti‐inflammatory MDSCs by iC3b activation via the CA beads in the GMA column.
影响因子:
20.3
作者:
Hsieh, Ching-Chuan;Chou, Hong-Shiue;Lu, Lina
通讯作者:
Lu, Lina
影响因子:
50.3
作者:
Yang, L;DeBusk, LM;Lin, PC
通讯作者:
Lin, PC