Ciciarello Marilena, Corradi Giulia, Loscocco Federica, Visani Giuseppe, Monaco Federica, Cavo Michele, Curti Antonio, Isidori Alessandro
Department of Experimental, Diagnostic and Specialty Medicine, Institute of Hematology "L. & A. Seràgnoli", University of Bologna, S. Orsola-Malpighi Hospital, Bologna, Italy.
Hematology and Stem Cell Transplant Center, AORMN Hospital, Pesaro, Italy.
Front Oncol. 2019 Oct 25;9:1135. doi: 10.3389/fonc.2019.01135. eCollection 2019.
Mesenchymal stromal cells (MSCs) have, for a long time, been recognized as pivotal contributors in the set up and maintenance of the hematopoietic stem cell (HSC) niche, as well as in the development and differentiation of the lympho-hematopoietic system. MSCs also have a unique immunomodulatory capacity, which makes them able to affect, both and , the function of immune cells. These features, namely the facilitation of stem cell engraftment and the inhibition of lymphocyte responses, have both proven essential for successful allogeneic stem cell transplantation (allo-SCT), which remains the only curative option for several hematologic malignancies. For example, in steroid-refractory acute graft-vs. host disease developing after allo-SCT, MSCs have produced significant results and are now considered a treatment option. However, more recently, the other side of the MSC coin has been unveiled, because of their emerging role in creating a protective and immune-tolerant microenvironment able to support the survival of leukemic cells and affect the response to therapies. In this light, it has been proposed that the failure of current treatments to efficiently override the stroma-mediated protection of leukemic cells accounts for the high rate of relapse in acute myeloid leukemia, at least in part. In this review, we will focus on emerging microenvironment-driven mechanisms conferring a survival advantage to leukemic cells overt physiological HSCs. This body of evidence increasingly highlights the opportunity to consider tumor-microenvironment interactions when designing new therapeutic strategies.
长期以来,间充质基质细胞(MSCs)一直被认为是造血干细胞(HSC)龛形成和维持以及淋巴造血系统发育和分化的关键贡献者。MSCs还具有独特的免疫调节能力,这使其能够影响免疫细胞的功能,包括正向和负向影响。这些特性,即促进干细胞植入和抑制淋巴细胞反应,已被证明对成功的异基因干细胞移植(allo-SCT)至关重要,而异基因干细胞移植仍然是几种血液系统恶性肿瘤的唯一治愈选择。例如,在allo-SCT后发生的类固醇难治性急性移植物抗宿主病中,MSCs已取得显著疗效,现在被视为一种治疗选择。然而,最近,MSCs的另一面被揭示出来,因为它们在创造一个能够支持白血病细胞存活并影响治疗反应的保护性和免疫耐受微环境中发挥着新出现的作用。有鉴于此,有人提出,目前的治疗方法未能有效克服基质介导的对白血病细胞的保护作用,至少部分地导致了急性髓系白血病的高复发率。在这篇综述中,我们将关注新兴的微环境驱动机制,这些机制赋予白血病细胞相对于正常生理HSCs的生存优势。这一系列证据越来越凸显了在设计新的治疗策略时考虑肿瘤-微环境相互作用的机会。