Kolloli Afsal, Subbian Selvakumar
Public Health Research Institute (PHRI) at New Jersey Medical School, Rutgers Biomedical and Health Sciences (RBHS), Rutgers University, The State University of New Jersey, Newark, NJ, United States.
Front Med (Lausanne). 2017 Oct 18;4:171. doi: 10.3389/fmed.2017.00171. eCollection 2017.
Tuberculosis (TB), caused by (), remains a leading cause of morbidity and mortality in humans worldwide. Currently, the standard treatment for TB involves multiple antibiotics administered for at least 6 months. Although multiple antibiotics therapy is necessary to prevent the development of drug resistance, the prolonged duration of treatment, combined with toxicity of drugs, contributes to patient non-compliance that can leads to the development of drug-resistant (MDR and XDR) strains. The existence of comorbid conditions, including HIV infection, not only complicates TB treatment but also elevates the mortality rate of patients. These facts underscore the need for the development of new and/or improved TB treatment strategies. Host-directed therapy (HDT) is a new and emerging concept in the treatment of TB, where host response is modulated by treatment with small molecules, with or without adjunct antibiotics, to achieve better control of TB. Unlike antibiotics, HDT drugs act by directly modulating host cell functions; therefore, development of drug resistance by infecting is avoided. Thus, HDT is a promising treatment strategy for the management of MDR- and XDR-TB cases as well as for patients with existing chronic, comorbid conditions such as HIV infection or diabetes. Functionally, HDT drugs fine-tune the antimicrobial activities of host immune cells and limit inflammation and tissue damage associated with TB. However, current knowledge and clinical evidence is insufficient to implement HDT molecules as a stand-alone, without adjunct antibiotics, therapeutic modality to treat any form of TB in humans. In this review, we discuss the recent findings on small molecule HDT agents that target autophagy, vitamin D pathway, and anti-inflammatory response as adjunctive agents along with standard antibiotics for TB therapy. Data from recent publications show that this approach has the potential to improve clinical outcome and can help to reduce treatment duration. Thus, HDT can contribute to global TB control programs by potentially increasing the efficiency of anti-TB treatment.
由()引起的结核病(TB)仍然是全球人类发病和死亡的主要原因。目前,结核病的标准治疗方法是使用多种抗生素至少治疗6个月。尽管使用多种抗生素治疗对于预防耐药性的产生是必要的,但治疗时间延长以及药物毒性会导致患者不依从,进而可能导致耐药(耐多药和广泛耐药)菌株的产生。包括艾滋病毒感染在内的合并症的存在,不仅使结核病治疗复杂化,还提高了患者的死亡率。这些事实凸显了开发新的和/或改进的结核病治疗策略的必要性。宿主导向疗法(HDT)是结核病治疗中一个新出现的概念,即通过小分子治疗来调节宿主反应,无论是否联合使用辅助抗生素,以更好地控制结核病。与抗生素不同,HDT药物通过直接调节宿主细胞功能发挥作用;因此,可避免感染菌产生耐药性。因此,HDT是治疗耐多药和广泛耐药结核病病例以及患有诸如艾滋病毒感染或糖尿病等现有慢性合并症患者的一种有前景的治疗策略。在功能上,HDT药物可微调宿主免疫细胞的抗菌活性,并限制与结核病相关的炎症和组织损伤。然而,目前的知识和临床证据不足以将HDT分子作为一种不联合辅助抗生素的独立治疗方式用于治疗人类任何形式的结核病。在本综述中,我们讨论了作为辅助药物与标准抗生素一起用于结核病治疗的、针对自噬、维生素D途径和抗炎反应的小分子HDT药物的最新研究结果。近期出版物的数据表明,这种方法有可能改善临床结果,并有助于缩短治疗时间。因此,HDT可能通过提高抗结核治疗的效率为全球结核病控制计划做出贡献。