Literature DB >> 32944493

Use of MSCs and MSC-educated macrophages to mitigate hematopoietic acute radiation syndrome.

Raghavan Chinnadurai1, Matthew H Forsberg2, John A Kink3,4, Peiman Hematti3,4, Christian M Capitini2,4.   

Abstract

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 a 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.

Entities:  

Year:  2020        PMID: 32944493      PMCID: PMC7491866          DOI: 10.1007/s40778-020-00176-0

Source DB:  PubMed          Journal:  Curr Stem Cell Rep


  96 in total

1.  Deletion of proapoptotic Puma selectively protects hematopoietic stem and progenitor cells against high-dose radiation.

Authors:  Lijian Shao; Yan Sun; Zhonghui Zhang; Wei Feng; Yongxing Gao; Zailong Cai; Zack Z Wang; A Thomas Look; Wen-Shu Wu
Journal:  Blood       Date:  2010-04-01       Impact factor: 22.113

2.  Response to the 'Comments on "Cellular Therapies for Treatment of Radiation Injury after a Mass Casualty Incident" (Radiat Res 2017; 188:242-45)' by Drouet et al. (Letters to the Editor, Radiat Res 2017; 188:463).

Authors:  R Tamarat; M Benderitter; J R Jourdain; B W Maidment; F Macchiarini; C I Rios; A L DiCarlo
Journal:  Radiat Res       Date:  2018-02-06       Impact factor: 2.841

3.  Immunological Markers of Chronic Occupational Radiation Exposure.

Authors:  Valentina L Rybkina; Maria V Bannikova; Galina V Adamova; Harald Dörr; Harry Scherthan; Tamara V Azizova
Journal:  Health Phys       Date:  2018-07       Impact factor: 1.316

4.  Cell, tissue and gene products with marketing authorization in 2018 worldwide.

Authors:  Natividad Cuende; John E J Rasko; Mickey B C Koh; Massimo Dominici; Laertis Ikonomou
Journal:  Cytotherapy       Date:  2018-10-24       Impact factor: 5.414

5.  MSC-based product characterization for clinical trials: an FDA perspective.

Authors:  Michael Mendicino; Alexander M Bailey; Keith Wonnacott; Raj K Puri; Steven R Bauer
Journal:  Cell Stem Cell       Date:  2014-02-06       Impact factor: 24.633

6.  Molecular Genetic and Immune Functional Responses Distinguish Bone Marrow Mesenchymal Stromal Cells from Hepatic Stellate Cells.

Authors:  Raghavan Chinnadurai; Jenna Sands; Devi Rajan; Xiao Liu; Dalia Arafat; Rahul Das; Frank A Anania; Greg Gibson; Tatiana Kisseleva; Jacques Galipeau
Journal:  Stem Cells       Date:  2019-05-09       Impact factor: 6.277

7.  Host origin of marrow stromal cells following allogeneic bone marrow transplantation.

Authors:  P J Simmons; D Przepiorka; E D Thomas; B Torok-Storb
Journal:  Nature       Date:  1987 Jul 30-Aug 5       Impact factor: 49.962

8.  Cryopreserved Mesenchymal Stromal Cells Are Susceptible to T-Cell Mediated Apoptosis Which Is Partly Rescued by IFNγ Licensing.

Authors:  Raghavan Chinnadurai; Ian B Copland; Marco A Garcia; Christopher T Petersen; Christopher N Lewis; Edmund K Waller; Allan D Kirk; Jacques Galipeau
Journal:  Stem Cells       Date:  2016-07-04       Impact factor: 6.277

9.  Adipose mesenchymal stromal cells minimize and repair radiation-induced oral mucositis.

Authors:  Osama Muhammad Maria; Mostafa Shalaby; Alasdair Syme; Nicoletta Eliopoulos; Thierry Muanza
Journal:  Cytotherapy       Date:  2016-07-14       Impact factor: 5.414

10.  Radiation rescue: mesenchymal stromal cells protect from lethal irradiation.

Authors:  Claudia Lange; Bärbel Brunswig-Spickenheier; Heike Cappallo-Obermann; Katharina Eggert; Ursula M Gehling; Cornelia Rudolph; Brigitte Schlegelberger; Kerstin Cornils; Jozef Zustin; Andrej-Nikolai Spiess; Axel R Zander
Journal:  PLoS One       Date:  2011-01-05       Impact factor: 3.240

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  2 in total

1.  Exosomes from primed MSCs can educate monocytes as a cellular therapy for hematopoietic acute radiation syndrome.

Authors:  Matthew H Forsberg; John A Kink; Anna S Thickens; Bryson M Lewis; Charlie J Childs; Peiman Hematti; Christian M Capitini
Journal:  Stem Cell Res Ther       Date:  2021-08-18       Impact factor: 6.832

2.  Dichotomic Potency of IFNγ Licensed Allogeneic Mesenchymal Stromal Cells in Animal Models of Acute Radiation Syndrome and Graft Versus Host Disease.

Authors:  Raghavan Chinnadurai; Paul D Bates; Keith A Kunugi; Kwangok P Nickel; Larry A DeWerd; Christian M Capitini; Jacques Galipeau; Randall J Kimple
Journal:  Front Immunol       Date:  2021-07-26       Impact factor: 7.561

  2 in total

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