Najar Mehdi, Raicevic Gordana, Crompot Emerence, Fayyad-Kazan Hussein, Bron Dominique, Toungouz Michel, Lagneaux Laurence
Laboratory of Clinical Cell Therapy, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Campus Erasme, Brussels, Belgium.
J Immunother. 2016 Feb-Mar;39(2):45-59. doi: 10.1097/CJI.0000000000000108.
Mesenchymal stromal cells (MSCs) have recently been the subject of great interest in the fields of regenerative medicine and immunotherapy due to their unique biological properties. In particular, MSCs possess immunoregulatory properties that can modulate immune as well as inflammatory responses. Although there are many studies about MSC immunomodulation, several complex and conflicting mechanisms have been reported. Herein, we aim to review these mechanisms and identify a link between these pathways. We focus on human studies in which bone marrow-derived MSCs and T cells were investigated. We propose that MSC-induced immunomodulation exists as a network where converging regulatory pathways compete to establish a tolerogenic state. As interleukin-10 seems to play a central role in this network, we also discuss the relationship between this cytokine and other regulatory factors in the context of immunomodulation.
间充质基质细胞(MSCs)由于其独特的生物学特性,近来在再生医学和免疫治疗领域备受关注。特别是,MSCs具有免疫调节特性,能够调节免疫反应以及炎症反应。尽管关于MSCs免疫调节的研究众多,但已报道了几种复杂且相互矛盾的机制。在此,我们旨在综述这些机制,并确定这些途径之间的联系。我们重点关注对人骨髓来源的MSCs和T细胞进行研究的人体实验。我们提出,MSC诱导的免疫调节以一个网络形式存在,在这个网络中,汇聚的调节途径相互竞争以建立一种耐受状态。由于白细胞介素-10似乎在这个网络中发挥核心作用,我们还在免疫调节的背景下讨论了这种细胞因子与其他调节因子之间的关系。