Mungan D, Sin B A, Celik G, Gürkan O U, Acican T, Misirligil Z
Department of Allergic Diseases, University of Ankara, Faculty of Medicine, Ankara, Türkiye.
Allergy Asthma Proc. 2001 Mar-Apr;22(2):87-91. doi: 10.2500/108854101778250643.
The rise in allergic disorders over the past three decades has been suggested to be related to the decrease in infectious diseases. Recently, a negative association between tuberculin responses and atopic disorders has also been reported. We planned to investigate the effect of natural exposure to Mycobacterium tuberculosis on atopic status in patients with active tuberculosis and to compare the findings with the data of patients with inactive disease. A total of 97 subjects were divided into two groups. Group 1, patients with proven active pulmonary tuberculosis (n = 66); group 2, subjects who had a history of previous tuberculous disease, with negative bacteriologic studies and no clinical and/or roentgenographic evidence of current disease (n = 31). Current history of allergic diseases was recorded by a physician with the use of a questionnaire adapted from the European Community Respiratory Health Survey (ECRHS), and skin-prick tests (SPTs) were performed using a standardized panel. Total IgE and Phadiatop were measured by the Pharmacia uniCAP system. The rate of one or more positive SPTs was significantly lower in the patients with active tuberculosis than the inactive group (15% versus 48.4%, p < 0.001). The current history of atopic diseases was 7.6% and 29% in the active and inactive tuberculosis groups, respectively (p = 0.002). The rate of positive skin tests to inhalant allergens in patients with inactive disease was higher than the rate of healthy adult Turkish people (48.4% versus 25%, p = 0.001). Geometric mean of total IgE levels were lower in patients with inactive disease than patients with active pulmonary tuberculosis (74.97 kU/L versus 106.3 kU/L, p = 0.05). The ratios of Phadiatop positivity were 21% and 38.7% in the active and inactive tuberculosis groups, respectively (p = 0.008). We found lower atopy rates in patients with active pulmonary tuberculosis than subjects with inactive disease. Although our data support the hypothesis that M. tuberculosis may prevent the development of atopic disorders by inducing the production of cytokines antagonistic to Th2 development, we believe prospective and experimental studies are needed before attributing a direct cause-effect link to this association.
在过去三十年中,过敏性疾病的增多被认为与传染病的减少有关。最近,也有报告称结核菌素反应与特应性疾病之间存在负相关。我们计划研究自然接触结核分枝杆菌对活动性肺结核患者特应状态的影响,并将研究结果与非活动性疾病患者的数据进行比较。总共97名受试者被分为两组。第1组为经证实的活动性肺结核患者(n = 66);第2组为既往有结核病史、细菌学检查阴性且无当前疾病的临床和/或影像学证据的受试者(n = 31)。由医生使用改编自欧洲共同体呼吸健康调查(ECRHS)的问卷记录过敏性疾病的当前病史,并使用标准化面板进行皮肤点刺试验(SPT)。使用Pharmacia uniCAP系统测量总IgE和Phadiatop。活动性肺结核患者中一项或多项SPT阳性的比例显著低于非活动性组(15%对48.4%,p < 0.001)。活动性和非活动性肺结核组中特应性疾病的当前病史分别为7.6%和29%(p = 0.002)。非活动性疾病患者对吸入性过敏原皮肤试验阳性的比例高于健康成年土耳其人(48.4%对25%,p = 0.001)。非活动性疾病患者的总IgE水平几何平均值低于活动性肺结核患者(74.97 kU/L对106.3 kU/L,p = 0.05)。活动性和非活动性肺结核组中Phadiatop阳性的比例分别为21%和38.7%(p = 0.008)。我们发现活动性肺结核患者的特应性发生率低于非活动性疾病患者。尽管我们的数据支持结核分枝杆菌可能通过诱导产生拮抗Th2发育的细胞因子来预防特应性疾病发展这一假说,但我们认为在将这种关联归因于直接的因果关系之前,还需要进行前瞻性和实验性研究。