Cázares-Sosa Fernando-Renato, Hernández-Solís Alejandro, Andrés-Dionicio Atenea-Estela, González-González Heliodora, Ibáñez-Hernández Miguel, Cicero-Sabido Raúl, Huerta Herón, Tapia-Romero Raquel, De-la-Rosa-Arana Jorge-Luis
Instituto de Diagnóstico y Referencia Epidemiológicos, Secretaria de Salud, Ciudad de México, México.
Servicio de Neumología, Hospital General de México, Ciudad de México, México.
J Infect Dev Ctries. 2019 Jan 31;13(1):28-34. doi: 10.3855/jidc.10583.
The sputum smear or the culture are the definitive diagnosis of pulmonary tuberculosis. Only a fraction of clinical patients are culture-confirmed.
A total of 24 clinical cases (40 ± 14 years old) with positive smear and negative co-morbidity were studied. Cases were selected from 600 patients who attended the pneumology service over two years. A sputum sample was cultured in Löwenstein-Jensen medium with consequent amplification of the rrnA V2 promoter, the differentiation region 4, and the IS6110 insertion sequence of Mycobacterium tuberculosis. After the culture result, the patients were divided into negative (n = 14) or positive (n = 10) culture groups. In addition, 30 samples from healthy donors (45 ± 10 years) were studied. The numbers of CD4, CD8 and CD19 lymphocytes were determined by flow cytometry. Levels of IgA and IgG to M. tuberculosis were measured by ELISA.
IgG and IgA levels were detected in patients with positive culture, while only IgA was found in patients with negative cultures. The lymphocyte populations in the two groups were similar. The presence of a pleural apical cap was found more frequently in patients with negative- (57%) than with positive cultures (10%).
The isotype profile in patients with positive cultures was both IgA and IgG positive, while in patients with negative culture, only IgA was found. The results will contribute to improve the diagnostic algorithm and appropriate treatment of patients with clinical tuberculosis. Further studies are needed to determine if this profile is predictive of the outcome of isolation.
痰涂片或培养是肺结核的确诊方法。只有一小部分临床患者通过培养得到确诊。
对24例涂片阳性且无合并症的临床病例(40±14岁)进行了研究。病例选自两年内到呼吸科就诊的600例患者。将痰标本接种于罗-琴培养基中,随后对结核分枝杆菌的rrnA V2启动子、差异区域4和IS6110插入序列进行扩增。培养结果出来后,将患者分为培养阴性组(n = 14)和培养阳性组(n = 10)。此外,还研究了30例健康供者(45±10岁)的样本。通过流式细胞术测定CD4、CD8和CD19淋巴细胞的数量。采用酶联免疫吸附测定法检测针对结核分枝杆菌的IgA和IgG水平。
培养阳性患者检测到IgG和IgA水平,而培养阴性患者仅检测到IgA。两组的淋巴细胞群体相似。胸膜尖帽在培养阴性患者(57%)中比培养阳性患者(10%)中更常见。
培养阳性患者的同种型谱为IgA和IgG均阳性,而培养阴性患者仅检测到IgA。这些结果将有助于改进临床结核病患者的诊断算法和适当治疗。需要进一步研究以确定该谱型是否可预测隔离结果。