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抗肿瘤坏死因子α制剂所致药物性狼疮。

Drug-induced lupus due to anti-tumor necrosis factor alpha agents.

作者信息

Costa Michelle F, Said Nuha R, Zimmermann Bernard

机构信息

Roger Williams Medical Center, Boston University School of Medicine, Providence, RI 02908, USA.

出版信息

Semin Arthritis Rheum. 2008 Jun;37(6):381-7. doi: 10.1016/j.semarthrit.2007.08.003. Epub 2007 Oct 30.

Abstract

PURPOSE

To evaluate the reported cases of drug-induced lupus erythematosus (DILE) due to anti-tumor necrosis factor (TNF) alpha therapy and to compare "classic" DILE with DILE secondary to anti-TNFalpha therapy. We also add 3 case reports related to 3 different anti-TNFalpha drugs to the literature.

METHODS

We searched the Medline database for cases published in English and evaluated 53 cases in 27 papers purported to be TNFalpha-induced DILE. We compared the clinical and laboratory features of cases that fulfilled our criteria for TNFalpha DILE to those of DILE due to non-TNFalpha drugs as found in standard texts. We also report the clinical and laboratory findings of our 3 patients with drug-induced lupus related to anti-TNFalpha drugs, 1 each in patients treated with adalimumab, etanercept, and infliximab.

RESULTS

Of the 53 purported cases of DILE due to anti-TNFalpha therapy, we excluded 17 with cutaneous manifestations alone and 3 with overlap syndromes and mixed connective tissue disease. In the 33 cases that met our criteria for systemic DILE, 21 cases were due to infliximab, 10 cases were due to etanercept, and only 2 cases were related to adalimumab. TNFalpha-blocker-induced DILE cases had a higher prevalence of antibodies to double-stranded DNA, rash, and hypocomplementemia than DILE due to other drugs. Fever is common in both types of DILE. Renal disease, which is rare in classic DILE, has been reported in cases of TNFalpha DILE.

CONCLUSIONS

TNFalpha DILE has significant clinical and laboratory manifestations which distinguish it from DILE due to drugs other than anti-TNF agents and may be difficult to diagnose in patients treated for autoimmune diseases. It is appropriate to consider whether all patients who are begun on anti-TNF therapy should have pretreatment serologic evaluation for systemic lupus erythematosus.

摘要

目的

评估已报道的因抗肿瘤坏死因子(TNF)α治疗导致的药物性红斑狼疮(DILE)病例,并将“经典”DILE与抗TNFα治疗继发的DILE进行比较。我们还在文献中增加了3例与3种不同抗TNFα药物相关的病例报告。

方法

我们在Medline数据库中检索英文发表的病例,并评估了27篇论文中声称由TNFα诱导的DILE的53例病例。我们将符合TNFα DILE标准的病例的临床和实验室特征与标准文献中因非TNFα药物导致的DILE的特征进行比较。我们还报告了3例与抗TNFα药物相关的药物性狼疮患者的临床和实验室检查结果,分别为接受阿达木单抗、依那西普和英夫利昔单抗治疗的患者各1例。

结果

在53例声称因抗TNFα治疗导致的DILE病例中,我们排除了仅表现为皮肤症状的17例和伴有重叠综合征及混合性结缔组织病的3例。在符合系统性DILE标准的33例病例中,21例由英夫利昔单抗引起,10例由依那西普引起,仅2例与阿达木单抗有关。与其他药物导致的DILE相比,TNFα阻滞剂诱导的DILE病例中双链DNA抗体、皮疹和低补体血症的发生率更高。发热在两种类型的DILE中都很常见。在经典DILE中罕见的肾脏疾病在TNFα DILE病例中已有报道。

结论

TNFα DILE具有显著的临床和实验室表现,使其有别于抗TNF药物以外的其他药物导致的DILE,对于接受自身免疫性疾病治疗的患者可能难以诊断。考虑所有开始接受抗TNF治疗的患者是否应进行系统性红斑狼疮的治疗前血清学评估是合适的。

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