Hoagland Daniel, Zhao Ying, Lee Richard E
Department of Chemical Biology and Therapeutics, St Jude Children's Research Hospital, MS#1000, Memphis, TN 38105, USA.
Mini Rev Med Chem. 2016;16(6):481-97. doi: 10.2174/1389557515666150722101723.
Pediatric tuberculosis is an underappreciated global epidemic estimated to afflict around half a million children worldwide. This problem has historically been overlooked, due in part to their low social status and the difficulty in diagnosis of tuberculosis in children. Children are more susceptible to tuberculosis infection and disease progression, including rapid dissemination into extrapulmonary infection sites. Treatment of pediatric tuberculosis infections has been traditionally built around agents used to treat the adult disease, but the disease pathology, drug pharmacokinetics and the safety window in children differs from the adult disease. This produces additional concerns for drug discovery and development of new agents. This review examines: (i) the safety concerns for current front and second line agents used to treat complex drug resistant infections and how this knowledge can be used to identify, prioritize and dose agents that may be better tolerated in pediatric populations; and (ii) the chemistry and suitability of new drugs in the clinical development pipeline for tuberculosis for the treatment of pediatric infections indicating several new agents may offer significant improvements for the treatment of multi-drug resistant tuberculosis in children.
儿童结核病是一种未得到充分重视的全球流行病,据估计全球约有50万儿童受其影响。这一问题在历史上一直被忽视,部分原因是儿童社会地位低下以及儿童结核病诊断困难。儿童更容易感染结核病并出现疾病进展,包括迅速播散至肺外感染部位。传统上,儿童结核病感染的治疗是围绕用于治疗成人疾病的药物进行的,但儿童的疾病病理、药物药代动力学和安全范围与成人疾病不同。这给新药的研发带来了更多担忧。本综述探讨了:(i)用于治疗复杂耐药感染的当前一线和二线药物的安全性问题,以及如何利用这些知识来识别、排序和确定在儿科人群中耐受性可能更好的药物剂量;(ii)处于结核病临床开发阶段的新药的化学性质和适用性,以用于治疗儿童感染,表明几种新药可能会显著改善儿童耐多药结核病的治疗。