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[与英夫利昔单抗/硫唑嘌呤治疗相关的药物性肺泡炎]

[Drug-induced alveolitis associated with infliximab/azathioprine therapy].

作者信息

El-Hag K, Dercken H-G, Prenzel R, Hölzle E

机构信息

Abteilung für Pneumologie, Pius Hospital Oldenburg, 26121 Oldenburg.

出版信息

Pneumologie. 2008 Apr;62(4):204-8. doi: 10.1055/s-2007-1016443. Epub 2008 Feb 13.

DOI:10.1055/s-2007-1016443
PMID:18270925
Abstract

BACKGROUND

TNF-alpha is known to play a decisive role as a pro-inflammatory cytokine in several autoimmune conditions. Its neutralisation by TNF-alpha antagonists such as infliximab (Remicade), a chimeric monoclonal anti-TNF-alpha antibody, may be beneficial in patients with active disease. These anticytokine drugs have been approved and are being increasingly used in the therapy of rheumatoid arthritis, ankylosing spondylitis, inflammatory bowel disease, psoriatic arthropathy and generalised psoriasis after established treatments have failed. Whenever therapy options are few, TNF-alpha antagonists are regarded as an effective, relatively safe and generally well-tolerated alternative, even if there is no detailed knowledge of their safety profile and possible long-term adverse events. In the respiratory tract an increased risk of viral, (myco-)bacterial, fungal and opportunistic infections has been observed. Furthermore, rare cases of severe fibrosing alveolitis in patients with concomitant immunosuppressant therapy or underlying lung disease have been reviewed recently.

CASE

We present a case of drug-induced alveolitis following infliximab and azathioprine for the treatment of severe, generalised psoriasis and atopic eczema without pre-existing lung disease. Withdrawal of both drugs achieved clinical and functional stabilisation, and the addition of prednisolone resulted in a rapid improvement.

CONCLUSION

As the pathophysiology of the pulmonary insult is unknown and since there are potentially serious adverse effects, we advise caution and close screening before and after initiation of TNF-alpha blockade, especially in patients with an underlying lung disease or with a combination of pneumotoxic agents.

摘要

背景

已知肿瘤坏死因子-α(TNF-α)作为一种促炎细胞因子在多种自身免疫性疾病中起决定性作用。用英夫利昔单抗(类克)等TNF-α拮抗剂进行中和,英夫利昔单抗是一种嵌合单克隆抗TNF-α抗体,可能对活动性疾病患者有益。这些抗细胞因子药物已获批准,并且在常规治疗失败后越来越多地用于类风湿性关节炎、强直性脊柱炎、炎症性肠病、银屑病关节炎和泛发性银屑病的治疗。每当治疗选择有限时,TNF-α拮抗剂就被视为一种有效、相对安全且耐受性良好的替代方案,即使对其安全性概况和可能的长期不良事件了解并不详细。在呼吸道中,已观察到病毒、(分支)杆菌、真菌和机会性感染的风险增加。此外,最近还回顾了在接受免疫抑制治疗或患有基础肺部疾病的患者中罕见的严重纤维化肺泡炎病例。

病例

我们报告一例在用英夫利昔单抗和硫唑嘌呤治疗严重泛发性银屑病和特应性皮炎且无基础肺部疾病的患者中发生药物性肺泡炎的病例。停用这两种药物后实现了临床和功能稳定,加用泼尼松龙后病情迅速改善。

结论

由于肺部损伤的病理生理学尚不清楚,且存在潜在的严重不良反应,我们建议在开始TNF-α阻断治疗之前和之后要谨慎并密切筛查,尤其是对于有基础肺部疾病或合并肺毒性药物的患者。

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