Nandlal Louansha, Perumal Rubeshan, Naidoo Kogieleum
Centre for the AIDS Programme of Research in South Africa (CAPRISA), South African Medical Research Council (SAMRC)-CAPRISA-TB-HIV Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal Nelson R Mandela School of Medicine, Durban, South Africa.
Infect Drug Resist. 2022 Aug 29;15:4971-4984. doi: 10.2147/IDR.S381643. eCollection 2022.
The recognition that drug-resistant tuberculosis (DR-TB) poses a major threat to global tuberculosis (TB) control efforts has catalysed the development of new and urgently needed TB diagnostics. The full beneficial impact of the subsequent flood of new TB diagnostic tests into the market can only be realised if these diagnostic tests are readily accessible to TB programs and contribute to improved patient outcomes. Although phenotypic drug-susceptibility testing remains the gold standard, an improved understanding of the relationship between mutations and different levels of drug resistance coupled with the advantages of molecular diagnostics could result in rapid molecular diagnostic tests replacing phenotypic drug-susceptibility testing. Successful diagnostics need to diagnose all forms of drug-resistant TB prevalent in each geographic region. Given the finite number and often limited availability of effective drugs for DR-TB, the diagnostic test must be able to detect all clinically important types of resistance to available anti-TB drugs. However, less comprehensive resistance profiling may be sufficient in settings where extensively drug-resistant TB (XDR-TB) and pre-XDR are absent. Rapid molecular diagnostic tests for DR-TB detection suitable for DR-TB endemic settings should be accurate, inexpensive, suitable to be performed on an easily accessible sample, detect prevalent circulating drug-resistant strains, and provide results within a short turnaround time to enable timely treatment initiation. In this review, we appraise the wide range of molecular diagnostics for DR-TB endorsed by the World Health Organisation, discuss the challenges in the development and rollout of rapid molecular DR-TB tests in low- and middle-income countries, and highlight user perspectives and cost-effectiveness factors that influence their utility.
耐药结核病(DR-TB)对全球结核病(TB)防控工作构成重大威胁,这一认识推动了新型且急需的结核病诊断方法的开发。只有当结核病防治项目能够方便地获取这些诊断检测方法,并有助于改善患者治疗效果时,随后大量新的结核病诊断检测方法涌入市场所带来的全部有益影响才能得以实现。尽管表型药敏试验仍是金标准,但对突变与不同耐药水平之间关系的进一步理解,再加上分子诊断方法的优势,可能会使快速分子诊断检测取代表型药敏试验。成功的诊断方法需要能够诊断出每个地理区域普遍存在的所有形式的耐药结核病。鉴于治疗耐多药结核病的有效药物数量有限且往往难以获得,诊断检测必须能够检测出对现有抗结核药物的所有临床上重要的耐药类型。然而,在没有广泛耐药结核病(XDR-TB)和准广泛耐药结核病的地区,不太全面的耐药谱分析可能就足够了。适用于耐多药结核病流行地区的耐多药结核病快速分子诊断检测应准确、廉价,适合对易于获取的样本进行检测,能够检测出流行的耐药菌株,并在短时间内给出结果以便及时开始治疗。在这篇综述中,我们评估了世界卫生组织认可的多种耐多药结核病分子诊断方法,讨论了在低收入和中等收入国家开发和推广耐多药结核病快速分子检测所面临的挑战,并强调了影响其效用的用户观点和成本效益因素。