Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease

被引:54
作者
Kelly, Kilian [1 ]
Rasko, John E. J. [2 ,3 ,4 ]
机构
[1] Cynata Therapeut Ltd, Cremorne, Vic, Australia
[2] Royal Prince Alfred Hosp, Dept Cell & Mol Therapies, Sydney, NSW, Australia
[3] Univ Sydney, Centenary Inst, Gene & Stem Cell Therapy Program, Sydney, NSW, Australia
[4] Univ Sydney, Fac Med & Hlth, Cent Clin Sch, Sydney, NSW, Australia
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 12卷
关键词
graft versus host disease (GvHD); mesenchymal stromal (stem) cell (MSC); stem cell; bone marrow transplant (BMT); allogeneic; STEROID-REFRACTORY ACUTE; CONSENSUS DEVELOPMENT PROJECT; STEM-CELLS; ACUTE GVHD; PEDIATRIC-PATIENTS; CLINICAL-TRIALS; GRADE III; THERAPY; ADULT; MARROW;
D O I
10.3389/fimmu.2021.761616
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Graft versus host disease (GvHD) is a life-threating complication of allogeneic hematopoietic stem cell transplantation, which is initially treated with high dose corticosteroids. Approximately 50% of acute GvHD cases are resistant to steroid treatment, and two-year mortality rates in those steroid-resistant patients exceed 80%. Chronic GvHD necessitates prolonged corticosteroid use, which is typically associated with limited efficacy and troublesome adverse effects. No agent has yet been established as an optimal second line therapy for either acute or chronic GvHD, but mesenchymal stromal cells (MSCs) have shown substantial promise. MSCs promote an immunosuppressive and immunoregulatory environment via multifactorial mechanisms, including: secretion of proteins/peptides/hormones; transfer of mitochondria; and transfer of exosomes or microvesicles containing RNA and other molecules. A large number of clinical studies have investigated MSCs from various sources as a treatment for acute and/or chronic GvHD. MSCs are generally safe and well tolerated, and most clinical studies have generated encouraging efficacy results, but response rates have varied. Confounding factors include variability in MSC donor types, production methodology and dose regimens, as well as variations in study design. It is well-established that extensive culture expansion of primary donor-derived MSCs leads to marked changes in functionality, and that there is a high level of inter-donor variability in MSC properties. However, recent manufacturing innovations may be capable of overcoming these problems. Further adequately powered prospective studies are required to confirm efficacy and establish the place of MSC therapy in the treatment of this condition.
引用
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页数:10
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