Use of MSCs and MSC-Educated Macrophages to Mitigate Hematopoietic Acute Radiation Syndrome

被引:13
作者
Chinnadurai, Raghavan [1 ]
Forsberg, Matthew H. [2 ]
Kink, John A. [3 ,4 ]
Hematti, Peiman [3 ,4 ]
Capitini, Christian M. [2 ,4 ]
机构
[1] Mercer Univ, Dept Biomed Sci, Sch Med, 1250 E 66th St, Savannah, GA 31404 USA
[2] Univ Wisconsin, Dept Pediat, Sch Med & Publ Hlth, Madison, WI USA
[3] Univ Wisconsin, Dept Med, Sch Med & Publ Hlth, Madison, WI USA
[4] Univ Wisconsin, Carbone Canc Ctr, Sch Med & Publ Hlth, Madison, WI USA
关键词
Mesenchymal Stromal/Stem Cells; MSC-educated Macrophages; MSC-exosome-educated Macrophages; Hematopoietic Acute Radiation Syndrome; Cell Therapy; Radiation Medical Countermeasure; MESENCHYMAL STROMAL CELLS; VERSUS-HOST-DISEASE; BONE-MARROW; STEM-CELLS; INTERNATIONAL-SOCIETY; CELLULAR THERAPIES; IONIZING-RADIATION; PERIPHERAL-BLOOD; CD34(+) CELLS; RES; 2017;
D O I
10.1007/s40778-020-00176-0
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Purpose of Review Innovative and minimally toxic treatment approaches are sorely needed for the prevention and treatment of hematopoietic acute radiation syndrome (H-ARS). Cell therapies have been increasingly studied for their potential use as countermeasures for accidental and intentional ionizing radiation exposures which can lead to fatal ARS. Mesenchymal stem/stromal cells (MSCs) are used in cell therapy that have shown promising results in preclinical studies of ARS and are being developed in clinical trials specifically for H-ARS. MSCs, MSC-educated macrophages (MEMs), and MSC-exosome-educated macrophages (EEMs) all have the potential to be used as adoptive cell therapies for H-ARS. Here, we review how MSCs have been reported to mitigate inflammation from radiation injury while also stimulating hematopoiesis during ARS. Recent Findings We discuss emerging work with immune cell subsets educated by MSCs, including MEMs and EEMs, in promoting hematopoiesis in xenogeneic models of ARS. We also discuss the first placental-derived MSC product to enter phase I trials, PLX-R18, and the challenges faced by bringing MSC and other cell therapies into the clinic for treating ARS. Summary Although MSCs, MEMs, and EEMs are potential cell therapy candidates in promoting hematopoietic HRS, challenges persist in translational clinical development of these products to the clinic. Whether any of these cellular therapies will be sufficient as stand-alone therapies to mitigate H-ARS or if they will be a bridging therapy that insures survival until a curative allogeneic hematopoietic stem cell transplant can be performed are the key questions that will have to be answered.
引用
收藏
页码:77 / 85
页数:9
相关论文
共 96 条
[1]   Cotransplantation of human stromal cell progenitors into preimmune fetal sheep results in early appearance of human donor cells in circulation and boosts cell levels in bone marrow at later time points after transplantation [J].
Almeida-Porada, G ;
Porada, CD ;
Tran, N ;
Zanjani, ED .
BLOOD, 2000, 95 (11) :3620-3627
[2]   Concise Review: Mesenchymal Stem Cells: From Roots to Boost [J].
Andrzejewska, Anna ;
Lukomska, Barbara ;
Janowski, Miroslaw .
STEM CELLS, 2019, 37 (07) :855-864
[3]  
Bandekar M, 2020, AM J TRANSPLANT
[4]   Umbilical cord tissue-derived mesenchymal stromal cells maintain immunomodulatory and angiogenic potencies after cryopreservation and subsequent thawing [J].
Barcia, Rita N. ;
Santos, Jorge M. ;
Teixeira, Mariana ;
Filipe, Mariana ;
Pereira, Ana Rita S. ;
Ministro, Augusto ;
Agua-Doce, Ana ;
Carvalheiro, Manuela ;
Gaspar, Maria Manuela ;
Miranda, Joana P. ;
Graca, Luis ;
Simoes, Sandra ;
Rosa Santos, Susana Constantino ;
Cruz, Pedro ;
Cruz, Helder .
CYTOTHERAPY, 2017, 19 (03) :360-370
[5]   Mesenchymal Stem Cells Remain Host-Derived Independent of the Source of the Stem-Cell Graft and Conditioning Regimen Used [J].
Bartsch, Kristina ;
Al-Ali, Haifa ;
Reinhardt, Annette ;
Franke, Christina ;
Hudecek, Michael ;
Kamprad, Manja ;
Tschiedel, Sabine ;
Cross, Michael ;
Niederwieser, Dietger ;
Gentilini, Chiara .
TRANSPLANTATION, 2009, 87 (02) :217-221
[6]   DNA-damage response in hematopoietic stem cells: an evolutionary trade-off between blood regeneration and leukemia suppression [J].
Biechonski, Shahar ;
Yassin, Muhammad ;
Milyavsky, Michael .
CARCINOGENESIS, 2017, 38 (04) :367-377
[7]  
Bolus NE, 2017, J NUCL MED TECHNOL, V45, P259, DOI 10.2967/jnmt.117.195230
[8]   Human Mesenchymal Stem Cell-Educated Macrophages Are a Distinct High IL-6-Producing Subset that Confer Protection in Graft-versus-Host-Disease and Radiation Injury Models [J].
Bouchlaka, Myriam N. ;
Moffitt, Andrea B. ;
Kim, Jaehyup ;
Kink, John A. ;
Bloom, Debra D. ;
Love, Cassandra ;
Dave, Sandeep ;
Hematti, Peiman ;
Capitini, Christian M. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2017, 23 (06) :897-905
[9]   Function of Cryopreserved Mesenchymal Stromal Cells With and Without Interferon- Prelicensing is Context Dependent [J].
Burand, Anthony J. ;
Gramlich, Oliver W. ;
Brown, Alex J. ;
Ankrum, James A. .
STEM CELLS, 2017, 35 (05) :1437-1439
[10]   The sensitivity of human mesenchymal stem cells to ionizing radiation [J].
Chen, Miao-Fen ;
Lin, Ching-Tai ;
Chen, Wen-g Chen ;
Yang, Cheng-Ta ;
Chen, Chih-g Chen ;
Liao, Shuen-Kuei ;
Liu, Jacqueline Ming ;
Lu, Chang-Hsien ;
Lee, Kuan-Der .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 66 (01) :244-253