Introna Martino, Rambaldi Alessandro
USC Ematologia, Azienda Ospedaliera Papa Giovanni XXIII, Bergamo, Italy.
Curr Opin Organ Transplant. 2015 Feb;20(1):72-8. doi: 10.1097/MOT.0000000000000158.
The aim of the present review was to give a critical opinion on the use of mesenchymal stromal cells (MSCs) to treat or to prevent graft-versus-host disease (GVHD).
The first part includes a summary of the many clinical trials published so far either to prevent or to treat GVHD in recipients of haematopoietic stem cell transplantation. We discuss in more detail a comparison in a subgroup of studies, including our own clinical work, which have in common the use of the platelet lysate to expand the MSCs from bone marrow origin.In the second part, we describe a few crucial elements of the biology of the GVHD and the biology of the MSCs themselves, showing their possible role in the immune modulation and in the inflammation in several in-vivo experimental models.
The complexity of the clinical condition that is the object of the trials and the paucity of information on the mechanisms of action in vivo of MSCs at different anatomical sites and in different times of the development of the disease preclude at the moment the identification of a strong rationale for MSC therapeutic schedule. Moreover, the typical development of GVHD requires different time points of clinical evaluation than those previously generally utilized in studies conducted on MSCs.
本综述旨在对间充质基质细胞(MSCs)用于治疗或预防移植物抗宿主病(GVHD)发表批判性意见。
第一部分总结了迄今为止发表的许多关于预防或治疗造血干细胞移植受者GVHD的临床试验。我们更详细地讨论了一组研究的比较,包括我们自己的临床工作,这些研究的共同之处在于使用血小板裂解物来扩增源自骨髓的MSCs。在第二部分中,我们描述了GVHD生物学和MSCs自身生物学的一些关键要素,展示了它们在几种体内实验模型中免疫调节和炎症方面可能发挥的作用。
作为试验对象的临床情况的复杂性以及关于MSCs在不同解剖部位和疾病发展不同阶段体内作用机制的信息匮乏,目前妨碍了确定MSCs治疗方案的有力理论依据。此外,GVHD的典型发展需要与先前在MSCs研究中普遍使用的临床评估时间点不同的时间点。