Connell Tom, Bar-Zeev Naor, Curtis Nigel
Infectious Diseases Unit, Department of General Medicine, University of Melbourne, Royal Children's Hospital Melbourne, Parkville, Australia.
Clin Infect Dis. 2006 Jun 1;42(11):e82-5. doi: 10.1086/503910. Epub 2006 Apr 27.
The diagnosis of perinatal tuberculosis (TB) is problematic because of its nonspecific presentation, the difficulty of obtaining microbiological confirmation, and the unreliability of the tuberculin skin test. Immunodiagnosis of TB has received new attention with the discovery of Mycobacterium tuberculosis-specific immunodominant antigens (early secreted antigenic target 6 [ESAT-6] and culture filtrate protein 10 [CFP-10]) that are encoded by the RD1 region of the pathogen. A whole blood assay has recently been developed to quantitatively measure interferon- gamma production by lymphocytes specific to these antigens, but its evaluation in the diagnosis of TB in infants and children has been limited to date.
In addition to routine diagnostic evaluation (tuberculin skin tests, culture of early-morning gastric aspirate samples, and chest radiographs), 2 infants with suspected perinatal TB were investigated with a whole blood interferon-gamma release assay.
The results of the tuberculin skin tests were negative for both patients. The findings of the chest radiographs were abnormal with features suggestive of miliary TB. A whole blood interferon- gamma release assay was performed and yielded positive results within 48 h after admission to the hospital for both patients, prompting early antituberculous treatment. M. tuberculosis was cultured after 6 weeks from gastric aspirate samples collected on admission to the hospital from both infants. At 6 months of age, both infants were thriving and had acheived normal developmental milestones.
The advent of interferon- gamma release assays may prove to be useful in the evaluation of infants with suspected perinatal TB.
围产期结核病(TB)的诊断存在问题,因为其临床表现不具特异性,难以获得微生物学确诊,且结核菌素皮肤试验不可靠。随着结核分枝杆菌特异性免疫优势抗原(早期分泌性抗原靶标6 [ESAT-6]和培养滤液蛋白10 [CFP-10])的发现,结核病的免疫诊断受到了新的关注,这些抗原由病原体的RD1区域编码。最近开发了一种全血检测方法,用于定量测量针对这些抗原的淋巴细胞产生的干扰素-γ,但迄今为止,其在婴幼儿结核病诊断中的评估有限。
除了常规诊断评估(结核菌素皮肤试验、清晨胃液抽吸样本培养和胸部X线片)外,还对2例疑似围产期结核病的婴儿进行了全血干扰素-γ释放检测。
两名患者的结核菌素皮肤试验结果均为阴性。胸部X线片检查结果异常,有粟粒性结核病的特征。进行了全血干扰素-γ释放检测,两名患者入院后48小时内结果均为阳性,促使早期进行抗结核治疗。从两名婴儿入院时采集的胃液抽吸样本中培养出结核分枝杆菌,时间为6周后。在6个月大时,两名婴儿均茁壮成长,达到了正常的发育里程碑。
干扰素-γ释放检测的出现可能证明对疑似围产期结核病的婴儿评估有用。