首页> 外文期刊>Clinical & developmental immunology. >Carbonic Anhydrases III and IV Autoantibodies in Rheumatoid Arthritis, Systemic Lupus Erythematosus, Diabetes, Hypertensive Renal Disease, and Heart Failure
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Carbonic Anhydrases III and IV Autoantibodies in Rheumatoid Arthritis, Systemic Lupus Erythematosus, Diabetes, Hypertensive Renal Disease, and Heart Failure

机译:类风湿关节炎,系统性红斑狼疮,糖尿病,高血压肾病和心力衰竭中的碳酸酐酶III和IV自身抗体

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In the present study, the CA III and IV autoantibodies, CA activity, antioxidant enzymes and cytokines in rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), diabetes, hypertensive renal disease, and heart failure were investigated. The anti-CA III antibody titers in patients with RA, SLE, and type 1 diabetes (T1D) were significantly higher than that in control groups ( P < 0.05). The anti-CA IV antibody titers in patients with RA, SLE, type 1 diabetic nephropathy (T1DN), and heart failure were significantly higher than that in control groups ( P < 0.05) while anti-CA IV antibody could suppress the total CA activity. The SOD and GPx levels in patients with RA, SLE, and T1DN were significantly lower than that in control groups ( P < 0.05). IL-6, IL-17, IFN- γ , and TNF- α levels were significantly higher in SLE group compared with the control group ( P < 0.05). Weak but significant correlations were found between anti-CA III antibodies and ESR in RA ( r = 0.403, P = 0.013) and SLE patients ( r = 0.397, P = 0.007). These results suggested that the generation of CA III and IV autoantibodies, antioxidant enzymes, and cytokines might influence each other and CA autoantibodies might affect the normal physiology function of CA.
机译:在本研究中,研究了类风湿关节炎(RA),系统性红斑狼疮(SLE),糖尿病,高血压肾病和心力衰竭的CA III和IV自身抗体,CA活性,抗氧化酶和细胞因子。 RA,SLE和1型糖尿病(T1D)患者的抗CA III抗体滴度显着高于对照组(P <0.05)。 RA,SLE,1型糖尿病肾病(T1DN)和心力衰竭患者的抗CA IV抗体滴度明显高于对照组(P <0.05),而抗CA IV抗体可抑制总CA活性。 RA,SLE和T1DN患者的SOD和GPx水平显着低于对照组(P <0.05)。 SLE组的IL-6,IL-17,IFN-γ和TNF-α水平明显高于对照组(P <0.05)。在RA(r = 0.403,P = 0.013)和SLE患者(r = 0.397,P = 0.007)中,抗CA III抗体与ESR之间存在弱但显着的相关性。这些结果表明,CA III和IV自身抗体,抗氧化酶和细胞因子的产生可能相互影响,CA自身抗体可能影响CA的正常生理功能。

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