首页|他克莫司联合利妥昔单抗治疗系统性红斑狼疮的临床疗效研究

他克莫司联合利妥昔单抗治疗系统性红斑狼疮的临床疗效研究

扫码查看
目的 探讨系统性红斑狼疮采用他克莫司联合利妥昔单抗治疗的临床疗效及对血清学指标、T淋巴细胞亚群的影响。方法 62 例系统性红斑狼疮患者,按随机数字表法分为对照组(31 例)和观察组(31例)。对照组患者单纯口服他克莫司治疗,观察组口服他克莫司以及静脉滴注利妥昔单抗治疗。比较两组患者治疗前后血清学指标(血清免疫球蛋白、血清单核细胞趋化蛋白 1 及血清补体C3、C4)、T淋巴细胞亚群(CD4+、CD8+、CD4+/CD8+)及临床疗效、不良反应发生情况。结果 观察组治疗后血清免疫球蛋白A(2。06±0。38)g/L、免疫球蛋白G(12。84±2。43)g/L、免疫球蛋白M(1。40±0。30)g/L、血清单核细胞趋化蛋白 1(90。48±32。84)pg/ml明显低于治疗前的(3。40±0。50)g/L、(20。35±4。26)g/L、(2。75±0。61)g/L、(368。88±41。10)pg/ml及对照组治疗后的(2。55±0。44)g/L、(15。58±2。56)g/L、(1。90±0。33)g/L、(166。38±30。65)pg/ml,血清补体C3(0。64±0。10)g/L、补体C4(0。22±0。04)g/L明显高于治疗前的(0。40±0。08)、(0。10±0。03)g/L及对照组治疗后的(0。50±0。11)、(0。13±0。04)g/L,差异显著(P<0。05);对照组治疗后血清免疫球蛋白A、免疫球蛋白G、免疫球蛋白M、单核细胞趋化蛋白 1 均低于治疗前,血清补体C3、补体C4 均高于治疗前,差异显著(P<0。05)。观察组治疗后CD4+(43。88±6。58)%、CD4+/CD8+(1。14±0。22)明显高于治疗前的(35。60±5。50)%、(0。86±0。15)及对照组治疗后的(39。33±6。24)%、(1。00±0。20),差异显著(P<0。05);对照组治疗后CD4+、CD4+/CD8+均高于治疗前,差异显著(P<0。05)。观察组临床总有效率为93。55%(29/31),明显高于对照组的70。97%(22/31),差异显著(χ2=5。415,P<0。05)。对照组不良反应发生率为32。26%(10/31),明显高于观察组的9。68%(3/31),差异显著(χ2=4。769,P<0。05)。结论 系统性红斑狼疮采用他克莫司联合利妥昔单抗治疗能够有效调节T淋巴细胞亚群紊乱,提升补体C3、C4表达水平,降低免疫球蛋白和单核细胞趋化蛋白 1 表达水平,有效抑制病情进展,提升临床治疗效果,临床安全性良好。
Study on clinical efficacy of tacrolimus combined with rituximab in the treatment of systemic lupus erythematosus
Objective To explore the clinical efficacy of tacrolimus combined with rituximab in the treatment of systemic lupus erythematosus,and its influence on serological indexes and T lymphocyte subsets.Methods 62 patients with systemic lupus erythematosus were divided into a control group(31 cases)and an observation group(31 cases)according to random number table method.The control group was treated with oral tacrolimus alone,and the observation group was treated with oral tacrolimus and intravenous rituximab.Patients in both groups were compared in terms of serological indicators(serum immunoglobulin,serum monocyte chemotactic protein-1,serum complement C3,C4)and T lymphocyte subsets(CD4+,CD8+,CD4+/CD8+)before and after treatment,clinical efficacy and occurrence of adverse reactions.Results After treatment,the observation group had serum immunoglobulin A of(2.06±0.38)g/L,immunoglobulin G of(12.84±2.43)g/L,immunoglobulin M of(1.40±0.30)g/L,and monocyte chemotactic protein-1 of(90.48±32.84)pg/ml,which were significantly lower than those before treatment(3.40±0.50)g/L,(20.35±4.26)g/L,(2.75±0.61)g/L,and(368.88±41.10)pg/ml and in the control group after treatment(2.55±0.44)g/L,(15.58±2.56)g/L,(1.90±0.33)g/L,and(166.38±30.65)pg/ml;the observation group had serum complement C3 of(0.64±0.10)g/L and complement C4 of(0.22±0.04)g/L,which were significantly higher than those before treatment(0.40±0.08)and(0.10±0.03)g/L and in the control group after treatment(0.50±0.11)and(0.13±0.04)g/L.The difference was significant(P<0.05).In the control group,the serum immunoglobulin A,immunoglobulin G,immunoglobulin M and monocyte chemotactic protein-1 were lower than those before treatment,and serum complement C3 and complement C4 were higher than those before treatment.The difference was significant(P<0.05).After treatment,CD4+of(43.88±6.58)%and CD4+/CD8+of(1.14±0.22)in the observation group were significantly higher than those before treatment(35.60±5.50)%and(0.86±0.15)and in the control group after treatment(39.33±6.24)%and(1.00±0.20).The difference was significant(P<0.05).CD4+and CD4+/CD8+in the control group after treatment were higher than those before treatment,and the difference was significant(P<0.05).The total effective rate of the observation group was 93.55%(29/31),which was significantly higher than the control group's 70.97%(22/31),and the difference was significant(χ2=5.415,P<0.05).The incidence of adverse reactions in the control group was 32.26%(10/31),which was significantly higher than the observation group's 9.68%(3/31),and the difference was significant(χ2=4.769,P<0.05).Conclusion Tacrolimus combined with rituximab treatment for systemic lupus erythematosus can effectively regulate T lymphocyte subsets,increase the expression levels of complement C3 and C4,reduce the expression levels of immunoglobulin and monocyte chemotactic protein-1,effectively inhibit the progression of the disease,improve the clinical treatment effect,and have high clinical safety.

Systemic lupus erythematosusTacrolimusRituximabClinical study

陈丽珍、陈红

展开 >

351100 莆田九十五医院风湿免疫科

系统性红斑狼疮 他克莫司 利妥昔单抗 临床研究

2024

中国现代药物应用
中国水利电力医学科学技术学会

中国现代药物应用

影响因子:0.862
ISSN:1673-9523
年,卷(期):2024.18(9)