Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease

被引:58
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
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
收藏
页数:10
相关论文
共 75 条
[21]   Treatment and management of graft-versus-host disease: improving response and survival [J].
Garnett, Catherine ;
Apperley, Jane F. ;
Pavlu, Jiri .
THERAPEUTIC ADVANCES IN HEMATOLOGY, 2013, 4 (06) :366-378
[22]  
Greinix HT, 2000, BLOOD, V96, P2426
[23]   Mesenchymal Stem Cell-Derived Exosomes and Other Extracellular Vesicles as New Remedies in the Therapy of Inflammatory Diseases [J].
Harrell, Carl Randall ;
Jovicic, Nemanja ;
Djonov, Valentin ;
Arsenijevic, Nebojsa ;
Volarevic, Vladislav .
CELLS, 2019, 8 (12)
[24]   Mesenchymal stromal cell therapy for steroid-refractory acute and chronic graft versus host disease: a phase 1 study [J].
Herrmann, Richard ;
Sturm, Marian ;
Shaw, Kathryn ;
Purtill, Duncan ;
Cooney, Julian ;
Wright, Matthew ;
Phillips, Michael ;
Cannell, Paul .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2012, 95 (02) :182-188
[25]   Incidence, risk factors, and outcomes of sclerosis in patients with chronic graft-versus-host disease [J].
Inamoto, Yoshihiro ;
Storer, Barry E. ;
Petersdorf, Effie W. ;
Nelson, J. Lee ;
Lee, Stephanie J. ;
Carpenter, Paul A. ;
Sandmaier, Brenda M. ;
Hansen, John A. ;
Martin, Paul J. ;
Flowers, Mary E. D. .
BLOOD, 2013, 121 (25) :5098-5103
[26]   Tolerance to Bone Marrow Transplantation: Do Mesenchymal Stromal Cells Still Have a Future for Acute or Chronic GvHD? [J].
Introna, Martino ;
Golay, Josee .
FRONTIERS IN IMMUNOLOGY, 2020, 11
[27]   Treatment of Graft versus Host Disease with Mesenchymal Stromal Cells: A Phase I Study on 40 Adult and Pediatric Patients [J].
Introna, Martino ;
Lucchini, Giovanna ;
Dander, Erica ;
Galimberti, Stefania ;
Rovelli, Attilio ;
Balduzzi, Adriana ;
Longoni, Daniela ;
Pavan, Fabio ;
Masciocchi, Francesca ;
Algarotti, Alessandra ;
Mico, Caterina ;
Grassi, Anna ;
Deola, Sara ;
Cavattoni, Irene ;
Gaipa, Giuseppe ;
Belotti, Daniela ;
Perseghin, Paolo ;
Parma, Matteo ;
Pogliani, Enrico ;
Golay, Josee ;
Pedrini, Olga ;
Capelli, Chiara ;
Cortelazzo, Sergio ;
D'Amico, Giovanna ;
Biondi, Andrea ;
Rambaldi, Alessandro ;
Biagi, Ettore .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2014, 20 (03) :375-381
[28]   Ruxolitinib for the treatment of steroid-refractory acute GVHD (REACH1): a multicenter, open-label phase 2 trial [J].
Jagasia, Madan ;
Perales, Miguel-Angel ;
Schroeder, Mark A. ;
Ali, Haris ;
Shah, Nirav N. ;
Chen, Yi-Bin ;
Fazal, Salman ;
Dawkins, Fitzroy W. ;
Arbushites, Michael C. ;
Tian, Chuan ;
Connelly-Smith, Laura ;
Howell, Michael D. ;
Khoury, H. Jean .
BLOOD, 2020, 135 (20) :1739-1749
[29]   National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: I. The 2014 Diagnosis and Staging Working Group Report [J].
Jagasia, Madan H. ;
Greinix, Hildegard T. ;
Arora, Mukta ;
Williams, Kirsten M. ;
Wolff, Daniel ;
Cowen, Edward W. ;
Palmer, Jeanne ;
Weisdorf, Daniel ;
Treister, Nathaniel S. ;
Cheng, Guang-Shing ;
Kerr, Holly ;
Stratton, Pamela ;
Duarte, Rafael F. ;
McDonald, George B. ;
Inamoto, Yoshihiro ;
Vigorito, Afonso ;
Arai, Sally ;
Datiles, Manuel B. ;
Jacobsohn, David ;
Heller, Theo ;
Kitko, Carrie L. ;
Mitchell, Sandra A. ;
Martin, Paul J. ;
Shulman, Howard ;
Wu, Roy S. ;
Cutler, Corey S. ;
Vogelsang, Georgia B. ;
Lee, Stephanie J. ;
Pavletic, Steven Z. ;
Flowers, Mary E. D. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2015, 21 (03) :389-401
[30]   Adipose tissue-derived mesenchymal stromal cells as part of therapy for chronic graft-versus-host disease: A phase I/II study [J].
Jurado, Manuel ;
De La Mata, Claudia ;
Ruiz-Garcia, Antonio ;
Lopez-Fernandez, Elisa ;
Espinosa, Olga ;
Jose Remigia, Maria ;
Moratalla, Lucia ;
Goterris, Rosa ;
Garcia-Martin, Paloma ;
Ruiz-Cabello, Francisco ;
Garzon, Sebastian ;
Jesus Pascual, Maria ;
Espigado, Ildefonso ;
Solano, Carlos .
CYTOTHERAPY, 2017, 19 (08) :927-936