Omoteso Omobolanle A, Fadaka Adewale O, Walker Roderick B, Khamanga Sandile M
Division of Pharmaceutics, Faculty of Pharmacy, Rhodes University, Makhanda 6139, South Africa.
Department of Anesthesia, Division of Pain Management, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Microorganisms. 2025 Mar 24;13(4):722. doi: 10.3390/microorganisms13040722.
Multidrug-resistant tuberculosis (MDR-TB) is a significant public health challenge globally, exacerbated by the limited efficacy of existing therapeutic approaches, prolonged treatment duration, and severe side effects. As drug resistance continues to emerge, innovative drug delivery systems and treatment strategies are critical to combating this crisis. This review highlights the molecular mechanisms underlying resistance to drugs in , such as genetic mutation, efflux pump activity, and biofilm formation, contributing to the persistence and difficulty in eradicating MDR-TB. Current treatment options, including second-line drugs, offer limited effectiveness, prompting the need for innovation of advanced therapies and drug delivery systems. The progression in drug discovery has resulted in the approval of innovative therapeutics, including bedaquiline and delamanid, amongst other promising candidates under investigation. However, overcoming the limitations of traditional drug delivery remains a significant challenge. Nanotechnology has emerged as a promising solution, with nanoparticle-based drug delivery systems offering improved bioavailability and targeted and controlled release delivery, particularly for pulmonary targeting and intracellular delivery to macrophages. Furthermore, the development of inhalable formulations and the potential of nanomedicines to bypass drug resistance mechanisms presents a novel approach to enhancing drug efficacy. Moreover, adjunctive therapies, including immune modulation and host-directed therapies, are being explored to improve treatment outcomes. Immunotherapies, such as cytokine modulation and novel TB vaccines, offer complementary strategies to the use of antibiotics in combating MDR-TB. Personalized medicine approaches, leveraging genomic profiling of both the pathogen and the host, offer promise in optimizing treatment regimens and minimizing drug resistance. This review underscores the importance of multidisciplinary approaches, combining drug discovery, advanced delivery system development, and immune modulation to address the complexities of treating MDR-TB. Continued innovation, global collaboration, and improved diagnostics are essential to developing practical, accessible, and affordable treatments for MDR-TB.
耐多药结核病(MDR-TB)是全球一项重大的公共卫生挑战,现有治疗方法疗效有限、治疗疗程延长以及严重的副作用使这一挑战更加严峻。随着耐药性不断出现,创新的药物递送系统和治疗策略对于应对这一危机至关重要。本综述重点介绍了耐多药结核病中耐药的分子机制,如基因突变、外排泵活性和生物膜形成,这些机制导致了耐多药结核病难以根除且持续存在。包括二线药物在内的当前治疗选择效果有限,这促使人们需要创新先进疗法和药物递送系统。药物研发的进展已促成了创新疗法的获批,包括贝达喹啉和德拉马尼,以及其他一些正在研究的有前景的候选药物。然而,克服传统药物递送的局限性仍然是一项重大挑战。纳米技术已成为一种有前景的解决方案,基于纳米颗粒的药物递送系统具有更高的生物利用度以及靶向和控释递送能力,特别是用于肺部靶向和巨噬细胞的细胞内递送。此外,可吸入制剂的开发以及纳米药物绕过耐药机制的潜力为提高药物疗效提供了一种新方法。此外,正在探索辅助疗法,包括免疫调节和宿主导向疗法,以改善治疗效果。免疫疗法,如细胞因子调节和新型结核病疫苗,为使用抗生素对抗耐多药结核病提供了补充策略。利用病原体和宿主的基因组分析的个性化医疗方法有望优化治疗方案并最大限度地减少耐药性。本综述强调了多学科方法的重要性,即将药物研发、先进递送系统开发和免疫调节相结合,以应对耐多药结核病治疗的复杂性。持续创新、全球合作以及改进诊断对于开发实用、可及且负担得起的耐多药结核病治疗方法至关重要。