Nasiri Mohammad J, Lutfy Kabir, Venketaraman Vishwanath
Department of Microbiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 19839-69411, Iran.
College of Pharmacy, Western University of Health Sciences, Pomona, CA 91766-1854, USA.
Vaccines (Basel). 2024 Dec 12;12(12):1397. doi: 10.3390/vaccines12121397.
Multidrug-resistant tuberculosis (MDR-TB) poses a significant global health threat, especially when it involves the central nervous system (CNS). Tuberculous meningitis (TBM), a severe manifestation of TB, is linked to high mortality rates and long-term neurological complications, further exacerbated by drug resistance and immune evasion mechanisms employed by Mycobacterium tuberculosis (Mtb). Although pulmonary TB remains the primary focus of research, MDR-TBM introduces unique challenges in diagnosis, treatment, and patient outcomes. The effectiveness of current treatments is frequently compromised by poor CNS penetration of anti-TB drugs and the necessity for prolonged therapy, which often involves considerable toxicity. This review explores the potential of cytokine-based adjunct immunotherapies for MDR-TBM, addressing the challenges of balancing pro-inflammatory and anti-inflammatory signals within the CNS. A central focus is the prospective role of glutathione, not only in reducing oxidative stress but also in enhancing host immune defenses against Mtb's immune evasion strategies. Furthermore, the development of vaccines aimed at upregulating glutathione synthesis in macrophages represents a promising strategy to bolster the immune response and improve treatment outcomes. By integrating glutathione and innovative vaccine approaches into MDR-TBM management, this review proposes a comprehensive strategy that targets Mtb directly while supporting immune modulation, with the potential to enhance patient outcomes and reduce treatment related adverse effects. We underscore the urgent need for further research into adjunctive therapies and immunomodulatory strategies to more effectively combat MDR-TBM.
耐多药结核病(MDR-TB)对全球健康构成重大威胁,尤其是当它累及中枢神经系统(CNS)时。结核性脑膜炎(TBM)是结核病的一种严重表现形式,与高死亡率和长期神经并发症相关,结核分枝杆菌(Mtb)采用的耐药性和免疫逃避机制进一步加剧了这种情况。尽管肺结核仍然是研究的主要重点,但耐多药结核性脑膜炎在诊断、治疗和患者预后方面带来了独特的挑战。当前治疗的有效性常常因抗结核药物在中枢神经系统中的渗透性差以及需要长期治疗(这通常涉及相当大的毒性)而受到影响。本综述探讨了基于细胞因子的辅助免疫疗法对耐多药结核性脑膜炎的潜力,解决了在中枢神经系统内平衡促炎和抗炎信号的挑战。一个核心关注点是谷胱甘肽的前瞻性作用,它不仅能减少氧化应激,还能增强宿主针对Mtb免疫逃避策略的免疫防御。此外,开发旨在上调巨噬细胞中谷胱甘肽合成的疫苗是增强免疫反应和改善治疗效果的一种有前景的策略。通过将谷胱甘肽和创新疫苗方法整合到耐多药结核性脑膜炎的管理中,本综述提出了一种全面的策略,该策略在支持免疫调节的同时直接针对Mtb,有可能改善患者预后并减少治疗相关的不良反应。我们强调迫切需要进一步研究辅助疗法和免疫调节策略,以更有效地对抗耐多药结核性脑膜炎。