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英国儿童结核病与人类免疫缺陷病毒合并感染凸显了对更好的治疗监测工具的需求:病例报告

Pediatric tuberculosis-human immunodeficiency virus co-infection in the United Kingdom highlights the need for better therapy monitoring tools: a case report.

作者信息

Evangelopoulos Dimitrios, Whittaker Elizabeth, Honeyborne Isobella, McHugh Timothy D, Klein Nigel, Shingadia Delane

机构信息

Centre for Clinical Microbiology, University College London, London, NW3 2PF, UK.

Present address: Laboratory of Mycobacterial Metabolism and Antibiotic Research, The Francis Crick Institute, London, NW1 1AT, UK.

出版信息

J Med Case Rep. 2017 Feb 26;11(1):52. doi: 10.1186/s13256-017-1222-6.

Abstract

BACKGROUND

Tuberculosis is an infection that requires at least 6 months of chemotherapy in order to clear the bacteria from the patient's lungs. Usually, therapeutic monitoring is dependent on smear microscopy where a decline in acid-fast bacilli is observed. However, this might not be indicative of the actual decline of bacterial load and thus other tools such as culture and molecular assays are required for patient management.

CASE PRESENTATION

Here, we report the case of a 12-year-old Black African boy co-infected with tuberculosis and human immunodeficiency virus who remained smear culture positive and liquid culture negative for a prolonged period of time following chemotherapy. In order to determine whether there was any live bacteria present in his specimens, we applied the newly developed molecular bacterial load assay that detects the presence of 16S ribosomal ribonucleic acid derived from the bacteria. Using this methodology, we were able to quantify his bacterial load and inform the management of his treatment in order to reduce the disease burden. Following this intervention he went on to make a complete recovery.

CONCLUSIONS

This case report highlights the value of improved biomarkers for monitoring the treatment of tuberculosis and the role of molecular assays such as the molecular bacterial load assay applied here. The molecular bacterial load assay detects bacterial ribonucleic acid which corresponds closely with the number of live bacilli as compared with polymerase chain reaction that detects deoxyribonucleic acid and may include dead bacteria.

摘要

背景

结核病是一种感染性疾病,需要至少6个月的化疗才能清除患者肺部的细菌。通常,治疗监测依赖于涂片显微镜检查,观察抗酸杆菌数量的下降。然而,这可能并不表明细菌载量的实际下降,因此患者管理需要其他工具,如培养和分子检测。

病例报告

在此,我们报告一例12岁的非洲黑人男孩,他同时感染了结核病和人类免疫缺陷病毒,化疗后长时间痰涂片培养呈阳性而液体培养呈阴性。为了确定其标本中是否存在活菌,我们应用了新开发的分子细菌载量检测方法,该方法可检测源自细菌的16S核糖体核糖核酸的存在。使用这种方法,我们能够量化他的细菌载量,并为其治疗管理提供依据,以减轻疾病负担。经过这次干预,他完全康复。

结论

本病例报告强调了改进的生物标志物在监测结核病治疗中的价值,以及本文应用的分子细菌载量检测等分子检测方法的作用。分子细菌载量检测方法检测的是细菌核糖核酸,与检测脱氧核糖核酸且可能包括死菌的聚合酶链反应相比,它与活菌数量密切相关。

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