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肿瘤坏死因子-α拮抗剂在慢性心力衰竭患者中的治疗潜力。

Therapeutic potential of tumour necrosis factor-alpha antagonists in patients with chronic heart failure.

机构信息

Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.

出版信息

Heart Lung Circ. 2013 May;22(5):323-7. doi: 10.1016/j.hlc.2012.12.002. Epub 2013 Jan 18.

Abstract

OBJECTIVES

Elevated levels of tumour necrosis factor alpha (TNF-alpha) are associated with the development of heart failure. TNF-alpha antagonists, etanercept (ETA) and infliximab (INF) have been used for treating different clinical conditions. Anti-TNF-alpha therapy did not show favourable results in patients with chronic heart failure (CHF). This review analyses the reasons for anti-TNF-alpha therapy failure in CHF patients; potential approaches for improved clinical outcome are also addressed.

DESIGN AND METHODS

Data analysis from clinical trials of CHF patients treated with ETA and INF.

RESULTS

In heart failure patients, ETA and INF therapy did not lead to improved clinical outcomes and high doses of INF were associated with worsening of cardiac events. This contrasts with the observation that these agents are associated with reduced cardiac events when used in patients with inflammatory diseases such as rheumatoid arthritis (RA).

CONCLUSIONS

Treatment of CHF patients with TNF-alpha antagonists did not show encouraging results. There is a need for the development of better treatment strategies for CHF. Perhaps, tailored anti-TNF-alpha therapy in relation to the TNF-alpha genotype of CHF patients and targeting of the cytokine gene expression via signalling pathway inhibitors may have useful clinical implications.

摘要

目的

肿瘤坏死因子-α(TNF-α)水平升高与心力衰竭的发展有关。肿瘤坏死因子-α拮抗剂依那西普(ETA)和英夫利昔单抗(INF)已被用于治疗不同的临床病症。抗 TNF-α 疗法并未在慢性心力衰竭(CHF)患者中显示出良好的效果。本综述分析了抗 TNF-α 疗法在 CHF 患者中失败的原因;还探讨了改善临床结局的潜在方法。

设计和方法

分析接受 ETA 和 INF 治疗的 CHF 患者临床试验的数据。

结果

在心力衰竭患者中,ETA 和 INF 治疗并未导致临床结局改善,高剂量 INF 与心脏事件恶化相关。这与观察到的情况形成对比,即当这些药物用于类风湿关节炎(RA)等炎症性疾病患者时,它们与减少心脏事件相关。

结论

TNF-α拮抗剂治疗 CHF 患者并未显示出令人鼓舞的结果。需要制定更好的 CHF 治疗策略。也许,针对 CHF 患者的 TNF-α 基因型进行个体化抗 TNF-α 治疗,并通过信号通路抑制剂靶向细胞因子基因表达,可能具有有用的临床意义。

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