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肿瘤坏死因子α阻断治疗下脊柱关节炎的变化面貌。

The changing face of spondyloarthropathies under TNF α blockade.

作者信息

Elkayam Ori, Litinsky Irena, Levartovsky David, Caspi Dan

机构信息

Department of Internal Medicine F , Tel Aviv University, Tel Aviv, Israel.

出版信息

Open Rheumatol J. 2008;2:53-7. doi: 10.2174/1874312900802010053. Epub 2008 Nov 14.

DOI:10.2174/1874312900802010053
PMID:19088872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2588090/
Abstract

OBJECTIVES

Tumor necrosis factor alpha (TNF-α ) therapy has been implicated in the development of autoimmune diseases. Our aim was to describe three patients with spondyloarthropathies who responded to infliximab, a chimeric monoclonal antibody specific for TNF-α but developed new symptoms of spondyloarthropathies. In parallel, a review of the literature on psoriasis induced by TNF-α blockers was undertaken.

RESULTS

The first patient had been suffering from ankylosing spondylitis (AS) for more than 12 years. Infliximab induced a remission of AS, but he developed overt Crohn's disease two years after starting treatment. The second patient had AS for more than 20 years. Infliximab had an excellent effect on his AS, but he developed palmo-plantar psoriasis a few months after initiating therapy with the drug. The third patient, whose long-term and severe psoriasis had responded to infliximab developed peripheral arthritis. A review of the literature revealed 63 cases of psoriasis induced by TNF-α blockers (33 on Infliximab, 16 on Etanercept and 14 on Adalimumab). The underlying diseases were variable, including all the spectrum of conditions for which TNF-α blockers are indicated. Patients developed psoriasis after a mean duration of treatment of 11 months. Interstingly, a substantial proportion of patients continued treatment with TNF α blockers, the psoriasis improving in a majorityof cases under topical treatment only.

CONCLUSION

While Infliximab may change the course of spondyloarthropathy, depressing the original symptoms it may uncover other occult aspects of these diseases.

摘要

目的

肿瘤坏死因子α(TNF-α)疗法与自身免疫性疾病的发生有关。我们的目的是描述3例脊柱关节病患者,他们对英夫利昔单抗(一种针对TNF-α的嵌合单克隆抗体)有反应,但出现了脊柱关节病的新症状。同时,对TNF-α阻滞剂诱发银屑病的文献进行了综述。

结果

首例患者患强直性脊柱炎(AS)超过12年。英夫利昔单抗使AS缓解,但在开始治疗两年后他出现了明显的克罗恩病。第二例患者患AS超过20年。英夫利昔单抗对其AS有很好的疗效,但在开始使用该药治疗几个月后他出现了掌跖银屑病。第三例患者长期严重银屑病对英夫利昔单抗有反应,之后出现了外周关节炎。文献综述显示有63例TNF-α阻滞剂诱发银屑病的病例(33例使用英夫利昔单抗,16例使用依那西普,14例使用阿达木单抗)。基础疾病各不相同,包括TNF-α阻滞剂所适用的所有疾病谱。患者在平均治疗11个月后出现银屑病。有趣的是,相当一部分患者继续使用TNF-α阻滞剂治疗,大多数患者仅通过局部治疗银屑病就有所改善。

结论

虽然英夫利昔单抗可能改变脊柱关节病的病程,抑制原有症状,但可能会暴露这些疾病其他隐匿的方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f23e/2588090/cf161a4a4dcf/TORJ-2-53_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f23e/2588090/cf161a4a4dcf/TORJ-2-53_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f23e/2588090/cf161a4a4dcf/TORJ-2-53_F1.jpg

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本文引用的文献

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J Eur Acad Dermatol Venereol. 2008 Mar;22(3):380-2. doi: 10.1111/j.1468-3083.2007.02335.x.
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New onset of Crohn's disease during treatment of active ankylosing spondylitis with etanercept.在用依那西普治疗活动性强直性脊柱炎期间新发克罗恩病。
J Rheumatol. 2008 Mar;35(3):532-6. Epub 2008 Jan 15.
3
Pustular psoriasis induced by infliximab.
依那西普致强直性脊柱炎并发克罗恩病 1 例报告及文献复习
Rheumatol Int. 2018 Nov;38(11):2157-2162. doi: 10.1007/s00296-018-4165-3. Epub 2018 Oct 6.
4
Treatment efficacy of etanercept and MTX combination therapy for ankylosing spondylitis hip joint lesion in Chinese population.依那西普联合甲氨蝶呤治疗中国人群强直性脊柱炎髋关节病变的疗效。
Rheumatol Int. 2012 Jun;32(6):1663-7. doi: 10.1007/s00296-011-1844-8. Epub 2011 Mar 9.
英夫利昔单抗诱导的脓疱型银屑病。
J Eur Acad Dermatol Venereol. 2007 Nov;21(10):1424-6. doi: 10.1111/j.1468-3083.2007.02230.x.
4
Autoimmune diseases induced by TNF-targeted therapies: analysis of 233 cases.肿瘤坏死因子靶向治疗诱发的自身免疫性疾病:233例分析
Medicine (Baltimore). 2007 Jul;86(4):242-251. doi: 10.1097/MD.0b013e3181441a68.
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