Joshi Lavanya, Chelluri Lakshmi Kiran, Gaddam Sumanlatha
Department of Immunology, Bhagwan Mahavir Medical Research Center, 10-1-1, A.C. Guards, Hyderabad, Andhra Pradesh, 500 004, India.
Transplant Immunology and Stem Cell Laboratory, Global Hospitals, Hyderabad, India.
Arch Immunol Ther Exp (Warsz). 2015 Dec;63(6):427-33. doi: 10.1007/s00005-015-0347-9. Epub 2015 Jun 23.
Multi-drug-resistant (MDR) tuberculosis is a major public health problem worldwide. Drug resistance arises due to non-compliance of antibiotic therapy. Herein, we explored the therapeutic options available ranging from conservative treatment approaches to alternate adjunct therapies such as mesenchymal stromal cell (MSC) therapy interventions. It is attractive to understand the scientific rationale of using cells as drugs, in particular mesenchymal stem/stromal cells. The review dwells and attempts to analyze the mechanistic approaches of the current treatment modalities to modern therapies. MSCs have demonstrated profound capacity to regenerate and repair. They appear to modulate that the activities of dendritic cells regulate T cells, both in vivo and in vitro. While there seems to be some benefit of such therapies, its use warrants further research. The merits and de-merits of autologous therapy/allogeneic therapy are ill understood. The challenges of requirement of large number of cells for infusion, the route of administration, choice of timing are complex issues that need to be addressed. Furthermore, the host immune responses, environmental factors and epigenetic mechanisms compound the problem. Although, clinical studies are being performed using autologous MSCs in different inflammatory models, it is important that such an intervention should be based on sound scientific rationale. The current review examines the immunomodulatory properties of MSCs, its interactions with other cell types, in assessing the basis for autologous/allogeneic cell-based therapies in the treatment of XDR/MDR tuberculosis.
耐多药(MDR)结核病是全球主要的公共卫生问题。耐药性是由于抗生素治疗不依从导致的。在此,我们探讨了从保守治疗方法到间充质基质细胞(MSC)治疗干预等替代辅助治疗方法等可用的治疗选择。了解将细胞用作药物,特别是间充质干/基质细胞的科学原理很有吸引力。该综述详细阐述并试图分析当前治疗方式到现代疗法的作用机制方法。间充质干细胞已显示出强大的再生和修复能力。它们似乎在体内和体外调节树突状细胞的活性来调节T细胞。虽然这种疗法似乎有一些益处,但其使用仍需进一步研究。自体疗法/同种异体疗法的优缺点尚不清楚。输注所需大量细胞的挑战、给药途径、时机选择是需要解决的复杂问题。此外,宿主免疫反应、环境因素和表观遗传机制使问题更加复杂。尽管正在不同炎症模型中使用自体间充质干细胞进行临床研究,但重要的是这种干预应基于合理的科学原理。本综述研究了间充质干细胞的免疫调节特性、其与其他细胞类型的相互作用,以评估基于自体/同种异体细胞的疗法治疗广泛耐药/耐多药结核病的依据。