Aix Marseille Université, URMITE, UM63, CNRS 7278, IRD 198, INSERM 1095, 13005 Marseille, France.
J Antimicrob Chemother. 2014 Jan;69(1):219-27. doi: 10.1093/jac/dkt310. Epub 2013 Aug 14.
Patients with classic Whipple's disease have a lifetime defect in immunity to Tropheryma whipplei and frequently develop treatment failures, relapses or reinfections. Empirical treatments were tested before culture was possible, but the only in vitro bactericidal treatment consists of a combination of doxycycline and hydroxychloroquine.
Our laboratory has been a reference centre since the first culturing of Tropheryma whipplei, and we have tested 27,000 samples by PCR and diagnosed 250 cases of classic Whipple's disease. We report here the clinical course of patients who were followed by one of our group.
Of 29 patients, 22 (76%) were previously treated with immunosuppressive drugs, 26 (90%) suffered from arthralgias and 22 (76%) exhibited weight loss. Intravenous initial treatment was paradoxically associated with an increased risk of failure (P = 0.0282). Treatment with doxycycline and hydroxychloroquine (± sulfadiazine or trimethoprim/sulfamethoxazole) was associated with a better outcome (0/13 failures), whereas all 14 patients who were first treated with trimethoprim/sulfamethoxazole and referred to us (P < 0.0001) experienced failure. Among the patients treated with doxycycline and hydroxychloroquine after previous antibiotic treatments, two presented with a reinfection caused by different T. whipplei strains. Finally, serum therapeutic drug monitoring allowed us to detect a lack of compliance in the only patient with failure among the 22 patients treated with lifetime doxycycline.
In vitro results were confirmed by clinical outcomes and trimethoprim/sulfamethoxazole was associated with failures. The recommended management is a combination of doxycycline and hydroxychloroquine for 1 year, followed by doxycycline for the patient's lifetime along with stringent therapeutic drug monitoring.
患有经典型惠尔氏病的患者终生对 Tropheryma whipplei 免疫缺陷,并且经常发生治疗失败、复发或再感染。在可以进行培养之前,已经测试了经验性治疗,但唯一的体外杀菌治疗是多西环素和羟氯喹的联合治疗。
自 Tropheryma whipplei 首次培养以来,我们的实验室一直是一个参考中心,我们通过 PCR 测试了 27000 个样本,并诊断了 250 例经典型惠尔氏病。我们在此报告由我们的一个小组随访的患者的临床过程。
在 29 名患者中,22 名(76%)曾接受过免疫抑制药物治疗,26 名(90%)患有关节痛,22 名(76%)有体重减轻。最初的静脉内治疗出乎意料地与治疗失败的风险增加相关(P = 0.0282)。多西环素和羟氯喹(±磺胺嘧啶或甲氧苄啶/磺胺甲恶唑)治疗与更好的结果相关(0/13 例治疗失败),而首次接受甲氧苄啶/磺胺甲恶唑治疗并转介给我们的 14 名患者(P < 0.0001)均治疗失败。在先前接受抗生素治疗后用多西环素和羟氯喹治疗的患者中,有 2 例因不同的 T. whipplei 菌株引起再感染。最后,血清治疗药物监测使我们能够检测到在接受多西环素终生治疗的 22 名患者中唯一治疗失败的患者缺乏依从性。
体外结果通过临床结果得到证实,甲氧苄啶/磺胺甲恶唑与治疗失败相关。推荐的治疗方法是多西环素和羟氯喹联合治疗 1 年,然后是多西环素终生治疗,并严格进行治疗药物监测。