Brehm Thomas Theo, Köhler Niklas, Grobbel Hans-Peter, Welling Jürgen, Mandalakas Anna Maria, Fava Vinicius, Schurr Erwin, Lange Christoph
Department of Clinical Infectious Diseases, Research Center Borstel, Leibniz Lung Center, Parkallee 35, Borstel, Germany.
German Center for Infection Research (DZIF), Partner Site Hamburg-Lübeck-Borstel-Riems, Germany.
Infection. 2025 Jan 21. doi: 10.1007/s15010-024-02470-z.
Deciding whether to provide preventive treatment to contacts of individuals with multidrug-resistant (MDR) tuberculosis is complex.
We present the diagnostic pathways, clinical course and outcome of tuberculosis treatment in eight siblings from a single family. Tuberculosis disease was diagnosed by Mycobacterium tuberculosis culture and molecular detection of M. tuberculosis-specific DNA from bronchopulmonary specimens using GeneXpert MTB/RIF. M. tuberculosis infection was diagnosed by an interferon-gamma release assay (IGRA; QuantiFERON-TB Gold Plus). Whole exome sequencing for genetic predisposition to mycobacterial infection was performed in one patient.
Six of eight siblings aged 16-20 years from a migrant family of Somali origin were diagnosed with pulmonary MDR tuberculosis over a 12-month period. The remaining male siblings, aged 11 and 14 years, were asymptomatic during contact investigation. Chest radiographs, computed tomography (CT) scans, sputum cultures and nucleic acid amplification tests were negative, and the IGRA did not detect M. tuberculosis infection. A repeat CT scan eight months later was unremarkable, and repeated sputum cultures remained negative. In the absence of sufficient evidence of M. tuberculosis infection, no preventive treatment was offered. At month seven of consistent clinical observation, both children were diagnosed with pulmonary tuberculosis; the older with advanced disease and subsequent post-tuberculosis lung disease. Whole exome sequencing revealed no Mendelian variant associated with susceptibility to mycobacterial infection.
When significant risk of tuberculosis transmission exists, close contacts of MDR tuberculosis patients should be offered preventive treatment with levofloxacin despite a negative IGRA test result.
决定是否对耐多药(MDR)结核病患者的接触者进行预防性治疗是复杂的。
我们介绍了来自一个家庭的八名兄弟姐妹的结核病诊断途径、临床病程和治疗结果。通过结核分枝杆菌培养以及使用GeneXpert MTB/RIF对支气管肺标本进行结核分枝杆菌特异性DNA的分子检测来诊断结核病。通过干扰素-γ释放试验(IGRA;QuantiFERON-TB Gold Plus)诊断结核分枝杆菌感染。对一名患者进行了全外显子组测序以检测对分枝杆菌感染的遗传易感性。
在12个月期间,来自索马里移民家庭的八名年龄在16至20岁的兄弟姐妹中有六人被诊断为肺部耐多药结核病。其余两名分别为11岁和14岁的男性兄弟姐妹在接触者调查期间无症状。胸部X光片、计算机断层扫描(CT)、痰培养和核酸扩增试验均为阴性,IGRA未检测到结核分枝杆菌感染。八个月后重复CT扫描无异常,重复痰培养仍为阴性。由于缺乏足够的结核分枝杆菌感染证据,未提供预防性治疗。在持续临床观察的第七个月,两名儿童均被诊断为肺结核;年龄较大的患有晚期疾病以及随后的肺结核后肺部疾病。全外显子组测序未发现与分枝杆菌感染易感性相关的孟德尔变异。
当存在显著的结核病传播风险时,尽管IGRA检测结果为阴性,耐多药结核病患者的密切接触者仍应接受左氧氟沙星预防性治疗。