Abstract:Objective To explore and analyze the levels of toll-like receptor 9 (TLR9) and nuclear factor-κB (NF-κB) in peripheral blood mononuclear cells (PBMCs) of patients with systemic lupus erythematosus (SLE) and its clinical significance. Methods Sixty SLE patients in the Department of Rheumatology and Immunology of our hospital from April 2013 to December 2014 were selected as the research objects, including 35 SLE patients in active stage as active group and 25 cases of SLE patients in remission stage as remission group. At the same time, 30 healthy cases in our hospital were selected as control group. TLR9 and NF-κB levels in PBMCs were compared between the three groups. The correlations of TLR9 and NF-κB levels in PBMCs with organ involvement and types of immunosuppressants were observed. Results The level of TLR9 in PBMCs of the active group was significantly lower than that of the remission group and the control group (P < 0.05). The level of TLR9 in PBMCs of the remission group was significantly lower than that of the control group (P < 0.05). The level of NF-κB in PBMCs in the active group was significantly lower than that of the remission group and the control group (P < 0.05). The level of NF-κB in PBMCs of the remission group was significantly lower than that of the control group (P < 0.05). The TLR9 in PBMCs in the patients with skin rash and decreased white blood cells was not significantly different from that in the patients without skin rash or decreased white blood cells (P > 0.05). The TLR9 level in PBMCs of the patients with fever, serositis or hematuria was significantly different from that of the patients without fever, serositis or hematuria (P < 0.05). There was no significant difference in the NF-κB level between the patients with and the patients without serositis or hematuria (P > 0.05). The level of NF-κB in PBMCs of the patients with serositis or hematuria was not significantly different from that of the patients without serositis or hematuria. The level of NF-κB in PBMCs of the patients with fever, rash or decreased white blood cells was statistically different from that in PBMCs of the patients with negative findings (P < 0.05). Conclusions TLR9 level significantly decreases while NF-κB level significantly increases in patients with systemic lupus erythematosus compared to that in normal population. Decreased TLR9 level is correlated with fever, serositis and hematuria. Increased NF-κB level is correlated with fever, rash and reduced white cell count. Close monitoring of TLR9 and NF-κB level changes in PBMCs of system lupus erythematosus patients has important value in clinical diagnosis and treatment of the disease.