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Impact of haplotypes of TNF in the natural course of infective endocarditis.TNF 单倍型对感染性心内膜炎自然病程的影响。
Clin Microbiol Infect. 2014 May;20(5):459-64. doi: 10.1111/1469-0691.12370. Epub 2013 Oct 25.
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Overview of safety of non-biologic and biologic DMARDs.非生物和生物 DMARDs 的安全性概述。
Rheumatology (Oxford). 2012 Dec;51 Suppl 6:vi37-43. doi: 10.1093/rheumatology/kes283.
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[Whipple disease revealed by anti-TNFα therapy].[抗TNFα治疗引发的惠普尔病]
Rev Med Interne. 2013 Feb;34(2):105-9. doi: 10.1016/j.revmed.2012.10.371. Epub 2012 Nov 28.
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Previous immunosuppressive therapy is a risk factor for immune reconstitution inflammatory syndrome in Whipple's disease.既往免疫抑制治疗是 Whipple 病免疫重建炎症综合征的一个危险因素。
Dig Liver Dis. 2012 Oct;44(10):880-2. doi: 10.1016/j.dld.2012.05.008. Epub 2012 Jun 15.
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Whipple's disease presenting with neurological symptoms in an immunosuppressed patient.一名免疫抑制患者出现神经症状的惠普尔病。
BMJ Case Rep. 2012 Jun 5;2012:bcr0220125882. doi: 10.1136/bcr.02.2012.5882.
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Intrafamilial circulation of Tropheryma whipplei, France.法国,旋毛虫属内家庭内循环。
Emerg Infect Dis. 2012 Jun;18(6):949-55. doi: 10.3201/eid1806.111038.
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Tropheryma whipplei endocarditis without gastrointestinal involvement.无胃肠道受累的惠普尔嗜组织菌心内膜炎
Interact Cardiovasc Thorac Surg. 2012 Jul;15(1):161-3. doi: 10.1093/icvts/ivs116. Epub 2012 Apr 11.
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Whipple's disease diagnosis following the use of TNF-α blockade.使用肿瘤坏死因子-α阻滞剂后诊断出惠普尔病。
Rheumatology (Oxford). 2012 May;51(5):946. doi: 10.1093/rheumatology/ker387. Epub 2011 Dec 16.
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High frequency of Tropheryma whipplei in culture-negative endocarditis.培养阴性心内膜炎中帚虫属的高频率。
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肿瘤坏死因子抑制剂治疗后并发惠普尔病和心内膜炎

Complicated Whipple's disease and endocarditis following tumor necrosis factor inhibitors.

作者信息

Marth Thomas

机构信息

Thomas Marth, Division of Internal Medicine, Krankenhaus Maria Hilf, 54550 Daun, Germany.

出版信息

World J Cardiol. 2014 Dec 26;6(12):1278-84. doi: 10.4330/wjc.v6.i12.1278.

DOI:10.4330/wjc.v6.i12.1278
PMID:25548618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4278163/
Abstract

AIM

To test whether treatment with tumor necrosis factor inhibitors (TNFI) is associated with complications of Tropheryma whipplei (T. whipplei) infection.

METHODS

Because unexplained arthritis is often the first Whipple's disease (WD) symptom, patients may undergo treatment with TNFI before diagnosis. This may influence the course of infection with T. whipplei, which causes WD, because host immune defects contribute to the pathogenesis of WD. A literature search and cross referencing identified 19 reports of TNFI treatment prior to WD diagnosis. This case-control study compared clinical data in patients receiving TNFI therapy (group I, n = 41) with patients not receiving TNFI therapy (group II, n = 61). Patients from large reviews served as controls (group III, n = 1059).

RESULTS

The rate of endocarditis in patient group I was significantly higher than in patient group II (12.2% in group I vs 1.6% in group II, P < 0.05), and group III (12.2% in group I vs 0.16% in group III, P < 0.01). Other, severe systemic or local WD complications such as pericarditis, fever or specific organ manifestations were increased also in group I as compared to the other patient groups. However, diarrhea and weight loss were somewhat less frequent in patient group I. WD is typically diagnosed with duodenal biopsy and periodic acid Schiff (PAS) staining. PAS-stain as standard diagnostic test had a very high percentage of false negative results (diagnostic failure in 63.6% of cases) in group I. Polymerase chain reaction (PCR) for T. whipplei was more accurate than PAS-stainings (diagnostic accuracy, rate of true positive tests 90.9% for PCR vs 36.4% for PAS, P < 0.01).

CONCLUSION

TNFI trigger severe WD complications, particularly endocarditis, and lead to false-negative PAS-tests. In case of TNFI treatment failure, infection with T. whipplei should be considered.

摘要

目的

检测肿瘤坏死因子抑制剂(TNFI)治疗是否与惠普尔嗜组织菌(T. whipplei)感染并发症相关。

方法

由于不明原因的关节炎常为惠普尔病(WD)的首发症状,患者可能在诊断前接受TNFI治疗。这可能会影响由T. whipplei感染引起的WD病程,因为宿主免疫缺陷在WD发病机制中起作用。通过文献检索和交叉引用,确定了19例WD诊断前接受TNFI治疗的报告。本病例对照研究比较了接受TNFI治疗的患者(I组,n = 41)和未接受TNFI治疗的患者(II组,n = 61)的临床数据。大型综述中的患者作为对照(III组,n = 1059)。

结果

I组患者的心内膜炎发生率显著高于II组(I组为12.2%,II组为1.6%,P < 0.05)和III组(I组为12.2%,III组为0.16%,P < 0.01)。与其他患者组相比,I组中其他严重的全身或局部WD并发症,如心包炎、发热或特定器官表现也有所增加。然而,I组患者腹泻和体重减轻的频率略低。WD通常通过十二指肠活检和过碘酸希夫(PAS)染色进行诊断。在I组中,作为标准诊断测试的PAS染色有很高比例的假阴性结果(63.6%的病例诊断失败)。针对T. whipplei的聚合酶链反应(PCR)比PAS染色更准确(诊断准确性,PCR的真阳性测试率为90.9%,PAS为36.4%,P < 0.01)。

结论

TNFI会引发严重的WD并发症,尤其是心内膜炎,并导致PAS测试出现假阴性。在TNFI治疗失败的情况下,应考虑T. whipplei感染。