Parasite-Host Biology, National Institute of Malaria Research, Sector-8, Dwarka, New Delhi, 110077, India.
Department of Genetics and Epigenetics, Institute of Nuclear Medicine & Allied Science, Timarpur, New Delhi, 110054, India.
Stem Cell Rev Rep. 2021 Dec;17(6):1993-2002. doi: 10.1007/s12015-021-10191-1. Epub 2021 Jun 12.
Mesenchymal stem cells (MSCs) are self-renewing, multi-potent heterogeneous stem cells that display strong tissue protective and restorative properties by differentiating into cells of the mesodermal lineages. In addition to multi-lineage differentiation capacity, MSCs play important roles in regulating immune responses, inflammation, and tissue regeneration. MSCs play a role in the outcome of the pathogenesis of several infectious diseases. A unique subset of MSCs accumulates in secondary lymphoid organs during malaria disease progression. These MSCs counteract the capacity of malaria parasites to subvert activating co-stimulatory molecules and to regulate expression of negative co-stimulatory molecules on T lymphocytes. Consequently, MSCs have the capacity to restore the functions of CD34 haematopoietic cells and CD4 and CD8 T cells during malaria infection. These observations suggest that cell-based therapeutics for intervention in malaria may be useful in achieving sterile clearance and preventing disease reactivation. In addition, MSCs provide host protection against malaria by reprogramming erythropoiesis through accelerated formation of colony-forming-units-erythroid (CFU-E) cells in the bone marrow. These findings suggest that MSCs are positive regulators of erythropoiesis, making them attractive targets for treatment of malarial anemia. MSC-based therapies, unlike anti-malarial drugs, display therapeutic effects by targeting a large variety of cellular processes rather than a single pathway. In the present review we focus on these recent research findings and discuss clinical applications of MSC-based therapies for malaria.
间充质干细胞(MSCs)是自我更新的多能异质性干细胞,通过向中胚层谱系细胞分化显示出强大的组织保护和修复特性。除了多谱系分化能力外,MSCs 在调节免疫反应、炎症和组织再生方面也发挥着重要作用。MSCs 在几种感染性疾病的发病机制中起作用。在疟疾疾病进展过程中,一种独特的 MSC 亚群在次级淋巴器官中积聚。这些 MSC 对抗疟原虫颠覆激活共刺激分子的能力,并调节 T 淋巴细胞上负共刺激分子的表达。因此,MSC 具有在疟疾感染期间恢复 CD34 造血细胞和 CD4 和 CD8 T 细胞功能的能力。这些观察结果表明,针对疟疾的基于细胞的治疗可能有助于实现无菌清除和防止疾病再激活。此外,MSC 通过加速骨髓中集落形成单位-红细胞(CFU-E)细胞的形成来重新编程红细胞生成,从而为宿主提供对疟疾的保护。这些发现表明 MSC 是红细胞生成的正调节剂,使它们成为治疗疟疾性贫血的有吸引力的靶标。与抗疟药物不同,基于 MSC 的治疗通过靶向多种细胞过程而不是单一途径发挥治疗作用。在本综述中,我们重点介绍了这些最近的研究发现,并讨论了基于 MSC 的治疗疟疾的临床应用。