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ISCT Committee Paper|Articles in Press

International society for cell & gene therapy stem cell engineering committee: Cellular therapies for the treatment of graft-versus-host-disease after hematopoietic stem cell transplant

Published:March 18, 2023DOI:https://doi.org/10.1016/j.jcyt.2023.02.007

      Abstract

      Background aims

      Allogeneic hematopoietic stem cell transplant is a curative approach for many malignant and non-malignant hematologic conditions. Despite advances in its prevention and treatment, the morbidity and mortality related to graft-versus-host disease (GVHD) remains. The mechanisms by which currently used pharmacologic agents impair the activation and proliferation of potentially alloreactive T cells reveal pathways essential for the detrimental activities of these cell populations. Importantly, these same pathways can be important in mediating the graft-versus-leukemia effect in recipients transplanted for malignant disease. This knowledge informs potential roles for cellular therapies such as mesenchymal stromal cells and regulatory T cells in preventing or treating GVHD. This article reviews the current state of adoptive cellular therapies focused on GVHD treatment.

      Methods

      We conducted a search for scientific literature in PubMed® and ongoing clinical trials in clinicaltrial.gov with the keywords “Graft-versus-Host Disease (GVHD),” “Cellular Therapies,” “Regulatory T cells (Tregs),” “Mesenchymal Stromal (Stem) Cells (MSCs),” “Natural Killer (NK) Cells,” “Myeloid-derived suppressor cells (MDSCs),” and “Regulatory B-Cells (B-regs).” All the published and available clinical studies were included.

      Results

      Although most of the existing clinical data focus on cellular therapies for GVHD prevention, there are observational and interventional clinical studies that explore the potential for cellular therapies to be safe modalities for GVHD treatment while maintaining the graft-versus-leukemia effect in the context of malignant diseases. However, there are multiple challenges that limit the broader use of these approaches in the clinical scenario.

      Conclusions

      There are many ongoing clinical trials to date with the promise to expand our actual knowledge on the role of cellular therapies for GVHD treatment in an attempt to improve GVHD-related outcomes in the near future.

      Key Words

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      References

        • Hamilton B.K.
        Current approaches to prevent and treat GVHD after allogeneic stem cell transplantation.
        Hematology. 2018; 2018: 228-235https://doi.org/10.1182/asheducation-2018.1.228
        • Martinez-Cibrian N.
        • Zeiser R.
        • Perez-Simon J.A.
        Graft-versus-host disease prophylaxis: pathophysiology-based review on current approaches and future directions.
        Blood Reviews. 2021; 48100792https://doi.org/10.1016/j.blre.2020.100792
        • Martini D.J.
        • Chen Y.B.
        • DeFilipp Z.
        Recent FDA approvals in the treatment of graft-versus-host disease.
        The Oncologist. 2022; https://doi.org/10.1093/oncolo/oyac076
        • Petersdorf E.W.
        • Stevenson P.
        • Bengtsson M.
        • de Santis D.
        • Dubois V.
        • Gooley T.
        • Horowitz M.M.
        • Hsu K.C.
        • Madrigal A.J.
        • Malkki M.
        • McKallor C.
        • Morishima Y.
        • Oudshoorn M.
        • Spellman S.
        • Villard J.
        • Carrington M.
        HLA-B leader and survivorship after HLA-mismatched unrelated donor transplantation.
        Blood. 2020; https://doi.org/10.1182/blood.2020005743
        • Stein-Thoeringer C.K.
        • Nichols K.B.
        • Lazrak A.
        • Docampo M.D.
        • Slingerland A.E.
        • Slingerland J.B.
        • Clurman A.G.
        • Armijo G.
        • Gomes A.L.C.
        • Shono Y.
        • Staffas A.
        • Burgos Da Silva M.
        • Devlin S.M.
        • Markey K.A.
        • Bajic D.
        • Pinedo R.
        • Tsakmaklis A.
        • Littmann E.R.
        • Pastore A.
        • van den Brink M.R.M.
        Lactose drives Enterococcus expansion to promote graft-versus-host disease.
        Science. 2019; 366: 1143-1149https://doi.org/10.1126/science.aax3760
        • Lazaryan A.
        • Weisdorf D.J.
        • DeFor T.
        • Brunstein C.G.
        • MacMillan M.L.
        • Bejanyan N.
        • Holtan S.
        • Blazar B.R.
        • Wagner J.E.
        • Arora M.
        Risk factors for acute and chronic graft-versus-host disease after allogeneic hematopoietic cell transplantation with umbilical cord blood and matched sibling donors.
        Biology of Blood and Marrow Transplantation. 2016; 22: 134-140https://doi.org/10.1016/j.bbmt.2015.09.008
        • Anasetti C.
        • Logan B.R.
        • Lee S.J.
        • Waller E.K.
        • Weisdorf D.J.
        • Wingard J.R.
        • Cutler C.S.
        • Westervelt P.
        • Woolfrey A.
        • Couban S.
        • Ehninger G.
        • Johnston L.
        • Maziarz R.T.
        • Pulsipher M.A.
        • Porter D.L.
        • Mineishi S.
        • McCarty J.M.
        • Khan S.P.
        • Anderlini P.
        • Confer D.L.
        Peripheral-blood stem cells versus bone marrow from unrelated donors.
        New England Journal of Medicine. 2012; 367: 1487-1496https://doi.org/10.1056/nejmoa1203517
        • Yu J.
        • Parasuraman S.
        • Shah A.
        • Weisdorf D.
        Mortality, length of stay and costs associated with acute graft-versus-host disease during hospitalization for allogeneic hematopoietic stem cell transplantation.
        Current Medical Research and Opinion. 2018; 35: 983-988https://doi.org/10.1080/03007995.2018.1551193
        • DeFilipp Z.
        • Alousi A.M.
        • Pidala J.A.
        • Carpenter P.A.
        • Onstad L.E.
        • Arai S.
        • Arora M.
        • Cutler C.S.
        • Flowers M.E.D.
        • Kitko C.L.
        • Chen G.L.
        • Lee S.J.
        • Hamilton B.K.
        Nonrelapse mortality among patients diagnosed with chronic GVHD: an updated analysis from the Chronic GVHD Consortium.
        Blood Advances. 2021; 5: 4278-4284https://doi.org/10.1182/bloodadvances.2021004941
        • Gooptu M.
        • Antin J.H.
        GVHD prophylaxis 2020.
        Frontiers in Immunology. 2021; 12https://doi.org/10.3389/fimmu.2021.605726
        • Cari L.
        • de Rosa F.
        • Nocentini G.
        • Riccardi C.
        Context-dependent effect of glucocorticoids on the proliferation, differentiation, and apoptosis of regulatory T cells: a review of the empirical evidence and clinical applications.
        International Journal of Molecular Sciences. 2019; 20: 1142https://doi.org/10.3390/ijms20051142
        • Ni M.
        • Wang L.
        • Ding Y.
        • Gong W.
        • Wang S.
        • Neuber B.
        • Schubert M.L.
        • Sauer T.
        • Hückelhoven-Krauss A.
        • Luft T.
        • Hegenbart U.
        • Schönland S.
        • Eckstein V.
        • Wang J.
        • Krüger W.
        • Müller-Tidow C.
        • Dreger P.
        • Schmitt M.
        • Schmitt A.
        Response to extracorporeal photopheresis therapy of patients with steroid-refractory/-resistant GVHD is associated with up-regulation of Th22 cells and Tfh cells.
        Cytotherapy. 2022; 24: 311-319https://doi.org/10.1016/j.jcyt.2021.09.008
        • Shen M.Z.
        • Li J.X.
        • Zhang X.H.
        • Xu L.P.
        • Wang Y.
        • Liu K.Y.
        • Huang X.J.
        • Hong S.D.
        • Mo X.D.
        Meta-analysis of interleukin-2 receptor antagonists as the treatment for steroid-refractory acute graft-versus-host disease.
        Frontiers in Immunology. 2021; 12https://doi.org/10.3389/fimmu.2021.749266
        • Stallone G.
        • Infante B.
        • di Lorenzo A.
        • Rascio F.
        • Zaza G.
        • Grandaliano G.
        mTOR inhibitors effects on regulatory T cells and on dendritic cells.
        Journal of Translational Medicine. 2016; 14https://doi.org/10.1186/s12967-016-0916-7
        • Iclozan C.
        • Yu Y.
        • Liu C.
        • Liang Y.
        • Yi T.
        • Anasetti C.
        • Yu X.Z.
        T helper17 cells are sufficient but not necessary to induce acute graft-versus-host disease.
        Biology of Blood and Marrow Transplantation. 2010; 16: 170-178https://doi.org/10.1016/j.bbmt.2009.09.023
        • Ogonek J.
        • Kralj Juric M.
        • Ghimire S.
        • Varanasi P.R.
        • Holler E.
        • Greinix H.
        • Weissinger E.
        Immune reconstitution after allogeneic hematopoietic stem cell transplantation.
        Frontiers in Immunology. 2016; 7https://doi.org/10.3389/fimmu.2016.00507
        • Pai C.C.S.
        • Hsiao H.H.
        • Sun K.
        • Chen M.
        • Hagino T.
        • Tellez J.
        • Mall C.
        • Blazar B.R.
        • Monjazeb A.
        • Abedi M.
        • Murphy W.J.
        Therapeutic benefit of bortezomib on acute graft-versus-host disease is tissue specific and is associated with interleukin-6 levels.
        Biology of Blood and Marrow Transplantation. 2014; 20: 1899-1904https://doi.org/10.1016/j.bbmt.2014.07.022
        • Solomon S.R.
        • Sizemore C.A.
        • Ridgeway M.
        • Zhang X.
        • Brown S.
        • Holland H.K.
        • Morris L.E.
        • Solh M.
        • Bashey A.
        Safety and efficacy of rituximab-based first line treatment of chronic GVHD.
        Bone Marrow Transplantation. 2018; 54: 1218-1226https://doi.org/10.1038/s41409-018-0399-7
        • Uraki R.
        • Imai M.
        • Ito M.
        • Shime H.
        • Odanaka M.
        • Okuda M.
        • Kawaoka Y.
        • Yamazaki S.
        Foxp3+ CD4+ regulatory T cells control dendritic cells in inducing antigen-specific immunity to emerging SARS-CoV-2 antigens.
        PLOS Pathogens. 2021; 17e1010085https://doi.org/10.1371/journal.ppat.1010085
        • Fantini M.C.
        Transforming growth factor induced FoxP3+ regulatory T cells suppress Th1 mediated experimental colitis.
        Gut. 2006; 55: 671-680https://doi.org/10.1136/gut.2005.072801
        • DiPaolo R.J.
        • Brinster C.
        • Davidson T.S.
        • Andersson J.
        • Glass D.
        • Shevach E.M.
        Autoantigen-specific TGF beta-induced Foxp3+ regulatory T cells prevent autoimmunity by inhibiting dendritic cells from activating autoreactive T cells.
        J. Immunol. 2007; 179: 4685-4693https://doi.org/10.4049/jimmunol.179.7.4685
        • Huter E.N.
        • Punkosdy G.A.
        • Glass D.D.
        • Cheng L.I.
        • Ward J.M.
        • Shevach E.M.
        TGF-beta-induced Foxp3+ regulatory T cells rescue scurfy mice.
        Eur. J. Immunol. 2008; 38: 1814-1821https://doi.org/10.1002/eji.200838346
        • Elias S.
        • Rudensky A.Y
        Therapeutic use of regulatory T cells for graft-versus-host disease.
        British Journal of Haematology. 2019; 187 (\): 25-38https://doi.org/10.1111/bjh.16157
        • Guo W.W.
        • Su X.H.
        • Wang M.Y.
        • Han M.Z.
        • Feng X.M.
        • Jiang E.L.
        Regulatory T cells in GVHD therapy.
        Frontiers in Immunology. 2021; 12https://doi.org/10.3389/fimmu.2021.697854
        • Nguyen V.H.
        • Zeiser R.
        • Negrin R.S.
        Role of naturally arising regulatory T cells in hematopoietic cell transplantation.
        Biology of Blood and Marrow Transplantation. 2006; 12: 995-1009https://doi.org/10.1016/j.bbmt.2006.04.009
        • di Ianni M.
        • Olioso P.
        • Giancola R.
        • Santarone S.
        • Natale A.
        • Papalinetti G.
        • Villanova I.
        • Baldoni S.
        • di Tommaso A.
        • Bonfini T.
        • Accorsi P.
        • di Bartolomeo P.
        Treg-protected donor lymphocyte infusions: a new tool to address the graft-versus-leukemia effect in the absence of graft-versus-host disease in patients relapsed after HSCT.
        International Journal of Hematology. 2017; 106: 860-864https://doi.org/10.1007/s12185-017-2292-3
        • Trzonkowski P.
        • Bieniaszewska M.
        • Juścińska J.
        • Dobyszuk A.
        • Krzystyniak A.
        • Marek N.
        • Myśliwska J.
        • Hellmann A.
        First-in-man clinical results of the treatment of patients with graft versus host disease with human ex vivo expanded CD4+CD25+CD127− T regulatory cells.
        Clinical Immunology. 2009; 133: 22-26https://doi.org/10.1016/j.clim.2009.06.001
        • Koreth J.
        • Matsuoka K.I.
        • Kim H.T.
        • McDonough S.M.
        • Bindra B.
        • Alyea E.P.
        • Armand P.
        • Cutler C.
        • Ho V.T.
        • Treister N.S.
        • Bienfang D.C.
        • Prasad S.
        • Tzachanis D.
        • Joyce R.M.
        • Avigan D.E.
        • Antin J.H.
        • Ritz J.
        • Soiffer R.J.
        Interleukin-2 and regulatory T cells in graft-versus-host disease.
        New England Journal of Medicine. 2011; 365: 2055-2066https://doi.org/10.1056/nejmoa1108188
        • Theil A.
        • Tuve S.
        • Oelschlägel U.
        • Maiwald A.
        • Döhler D.
        • Oßmann D.
        • Zenkel A.
        • Wilhelm C.
        • Middeke J.M.
        • Shayegi N.
        • Trautmann-Grill K.
        • von Bonin M.
        • Platzbecker U.
        • Ehninger G.
        • Bonifacio E.
        • Bornhäuser M.
        Adoptive transfer of allogeneic regulatory T cells into patients with chronic graft-versus-host disease.
        Cytotherapy. 2015; 17: 473-486https://doi.org/10.1016/j.jcyt.2014.11.005
        • Koreth J.
        • Kim H.T.
        • Jones K.T.
        • Lange P.B.
        • Reynolds C.G.
        • Chammas M.J.
        • Dusenbury K.
        • Whangbo J.
        • Nikiforow S.
        • Alyea E.P.
        • Armand P.
        • Cutler C.S.
        • Ho V.T.
        • Chen Y.B.
        • Avigan D.
        • Blazar B.R.
        • Antin J.H.
        • Ritz J.
        • Soiffer R.J.
        Efficacy, durability, and response predictors of low-dose interleukin-2 therapy for chronic graft-versus-host disease.
        Blood. 2016; 128: 130-137https://doi.org/10.1182/blood-2016-02-702852
        • Whangbo J.S.
        • Kim H.T.
        • Mirkovic N.
        • Leonard L.
        • Poryanda S.
        • Silverstein S.
        • Kim S.
        • Reynolds C.G.
        • Rai S.C.
        • Verrill K.
        • Lee M.A.
        • Margossian S.
        • Duncan C.
        • Lehmann L.
        • Huang J.
        • Nikiforow S.
        • Alyea E.P.
        • Armand P.
        • Cutler C.S.
        • Koreth J.
        Dose-escalated interleukin-2 therapy for refractory chronic graft-versus-host disease in adults and children.
        Blood Advances. 2019; 3: 2550-2561https://doi.org/10.1182/bloodadvances.2019000631
        • Whangbo J.
        • Nikiforow S.
        • Kim H.T.
        • Wahl J.
        • Reynolds C.G.
        • Chamling Rai S.
        • Kim S.
        • Burden A.T.
        • Alho A.
        • Lacerda J.F.
        • Alyea E.P.
        • Cutler C.S.
        • Ho V.T.
        • Antin J.H.
        • Soiffer R.J.
        • Ritz J.
        • Koreth J.
        A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease.
        Blood Advances. 2022; https://doi.org/10.1182/bloodadvances.2021006625
        • Donato V.
        • Kim H.T.
        • Stowe P.
        • Reynolds C.G.
        • Ritz J.
        • Koreth J.
        • Whangbo J.S.
        Durability of clinical and immunologic responses to extended low-dose interleukin-2 therapy in patients with refractory chronic graft-versus-host disease.
        Frontiers in Immunology. 2022; 13https://doi.org/10.3389/fimmu.2022.954966
        • Brunstein C.G.
        • Miller J.S.
        • McKenna D.H.
        • Hippen K.L.
        • DeFor T.E.
        • Sumstad D.
        • Curtsinger J.
        • Verneris M.R.
        • MacMillan M.L.
        • Levine B.L.
        • Riley J.L.
        • June C.H.
        • Le C.
        • Weisdorf D.J.
        • McGlave P.B.
        • Blazar B.R.
        • Wagner J.E.
        Umbilical cord blood–derived T regulatory cells to prevent GVHD: kinetics, toxicity profile, and clinical effect.
        Blood. 2016; 127: 1044-1051https://doi.org/10.1182/blood-2015-06-653667
        • Betts B.C.
        • Pidala J.
        • Kim J.
        • Mishra A.
        • Nishihori T.
        • Perez L.
        • Ochoa-Bayona J.L.
        • Khimani F.
        • Walton K.
        • Bookout R.
        • Nieder M.
        • Khaira D.K.
        • Davila M.
        • Alsina M.
        • Field T.
        • Ayala E.
        • Locke F.L.
        • Riches M.
        • Kharfan-Dabaja M.
        • Anasetti C.
        IL-2 promotes early Treg reconstitution after allogeneic hematopoietic cell transplantation.
        Haematologica. 2017; 102: 948-957https://doi.org/10.3324/haematol.2016.153072
        • MacMillan M.L.
        • Hippen K.L.
        • McKenna D.H.
        • Kadidlo D.
        • Sumstad D.
        • DeFor T.E.
        • Brunstein C.G.
        • Holtan S.G.
        • Miller J.S.
        • Warlick E.D.
        • Weisdorf D.J.
        • Wagner J.E.
        • Blazar B.R.
        First-in-human phase 1 trial of induced regulatory T cells for graft-versus-host disease prophylaxis in HLA-matched siblings.
        Blood Advances. 2021; 5: 1425-1436https://doi.org/10.1182/bloodadvances.2020003219
        • Mishra S.
        • Srinivasan S.
        • Ma C.
        • Zhang N.
        Cd8+ regulatory T cellࣧa mystery to be revealed.
        Frontiers in Immunology. 2021; 12https://doi.org/10.3389/fimmu.2021.708874
        • Horwitz E.M.
        • Andreef M.
        • Frassoni F.
        Mesenchymal stromal cells.
        Current Opinion in Hematology. 2006; 13: 419-425https://doi.org/10.1097/01.moh.0000245697.54887.6f
        • Ryan M.M.
        • Patel M.
        • Hogan K.
        • Lipat A.J.
        • Scandolara R.
        • Das R.
        • Bruker C.
        • Galipeau J.
        • Chinnadurai R.
        Ruxolitinib inhibits IFNγ licensing of human bone marrow derived mesenchymal stromal cells.
        Transplantation and Cellular Therapy. 2021; 27: 389.e1-389.e10https://doi.org/10.1016/j.jtct.2021.02.002
        • Goto T.
        • Murata M.
        • Nishida T.
        • Terakura S.
        • Kamoshita S.
        • Ishikawa Y.
        • Ushijima Y.
        • Adachi Y.
        • Suzuki S.
        • Kato K.
        • Hirakawa A.
        • Nishiwaki S.
        • Nishio N.
        • Takahashi Y.
        • Kodera Y.
        • Matsushita T.
        • Kiyoi H.
        Phase I clinical trial of intra-bone marrow cotransplantation of mesenchymal stem cells in cord blood transplantation.
        Stem Cells Translational Medicine. 2020; 10: 542-553https://doi.org/10.1002/sctm.20-0381
        • Le Blanc K.
        • Rasmusson I.
        • Sundberg B.
        • Götherström C.
        • Hassan M.
        • Uzunel M.
        • Ringdén O
        Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells.
        The Lancet. 2004; 363: 1439-1441https://doi.org/10.1016/s0140-6736(04)16104-7
        • Le Blanc K.
        • Frassoni F.
        • Ball L.
        • Locatelli F.
        • Roelofs H.
        • Lewis I.
        • Lanino E.
        • Sundberg B.
        • Bernardo M.E.
        • Remberger M.
        • Dini G.
        • Egeler R.M.
        • Bacigalupo A.
        • Fibbe W.
        • Ringdén O
        Mesenchymal stem cells for treatment of steroid-resistant, severe, acute graft-versus-host disease: a phase II study.
        The Lancet. 2008; 371: 1579-1586https://doi.org/10.1016/s0140-6736(08)60690-x
        • Bader P.
        • Kuçi Z.
        • Bakhtiar S.
        • Basu O.
        • Bug G.
        • Dennis M.
        • Greil J.
        • Barta A.
        • Kállay K.M.
        • Lang P.
        • Lucchini G.
        • Pol R.
        • Schulz A.
        • Sykora K.W.
        • von Luettichau I.
        • Herter-Sprie G.
        • Uddin M.A.
        • Jenkin P.
        • Alsultan A.
        • Kuçi S.
        Effective treatment of steroid and therapy-refractory acute graft-versus-host disease with a novel mesenchymal stromal cell product (MSC-FFM).
        Bone Marrow Transplantation. 2018; 53: 852-862https://doi.org/10.1038/s41409-018-0102-z
        • Perez-Simon J.A.
        • Lopez-Villar O.
        • Andreu E.J.
        • Rifon J.
        • Muntion S.
        • Campelo M.D.
        • Sánchez-Guijo F.M.
        • Martinez C.
        • Valcarcel D.
        • Canizo C.D.
        Mesenchymal stem cells expanded in vitro with human serum for the treatment of acute and chronic graft-versus-host disease: results of a phase I/II clinical trial.
        Haematologica. 2011; 96: 1072-1076https://doi.org/10.3324/haematol.2010.038356
        • Prasad V.K.
        • Lucas K.G.
        • Kleiner G.I.
        • Talano J.A.M.
        • Jacobsohn D.
        • Broadwater G.
        • Monroy R.
        • Kurtzberg J.
        Efficacy and safety of ex vivo cultured adult human mesenchymal stem cells (ProchymalTM) in pediatric patients with severe refractory acute graft-versus-host disease in a compassionate use study.
        Biology of Blood and Marrow Transplantation. 2011; 17: 534-541https://doi.org/10.1016/j.bbmt.2010.04.014
        • Kurtzberg J.
        • Prockop S.
        • Teira P.
        • Bittencourt H.
        • Lewis V.
        • Chan K.W.
        • Horn B.
        • Yu L.
        • Talano J.A.
        • Nemecek E.
        • Mills C.R.
        • Chaudhury S.
        Allogeneic human mesenchymal stem cell therapy (remestemcel-L, prochymal) as a rescue agent for severe refractory acute graft-versus-host disease in pediatric patients.
        Biology of Blood and Marrow Transplantation. 2014; 20: 229-235https://doi.org/10.1016/j.bbmt.2013.11.001
        • Kurtzberg J.
        • Prockop S.
        • Chaudhury S.
        • Horn B.
        • Nemecek E.
        • Prasad V.
        • Satwani P.
        • Teira P.
        • Hayes J.
        • Burke E.
        Study 275: Updated expanded access program for remestemcel-l in steroid-refractory acute graft-versus-host disease in children.
        Biology of Blood and Marrow Transplantation. 2020; 26: 855-864https://doi.org/10.1016/j.bbmt.2020.01.026
      1. Mesoblast. Mesoblast receives complete response letter from the FDA for biologics license application for steroid-refractory acute graft versus host disease in children. Retrieved on October 5, 2020 from https://www.asx.com.au/asxpdf/20201002/pdf/44n8xx22956c1c.pdf.

        • Ringdén O.
        • Uzunel M.
        • Rasmusson I.
        • Remberger M.
        • Sundberg B.
        • Lönnies H.
        • Marschall H.U.
        • Dlugosz A.
        • Szakos A.
        • Hassan Z.
        • Omazic B.
        • Aschan J.
        • Barkholt L.
        • le Blanc K.
        Mesenchymal stem cells for treatment of therapy-resistant graft-versus-host disease.
        Transplantation. 2006; 81: 1390-1397https://doi.org/10.1097/01.tp.0000214462.63943.14
        • von Bonin M.
        • Stölzel F.
        • Goedecke A.
        • Richter K.
        • Wuschek N.
        • Hölig K.
        • Platzbecker U.
        • Illmer T.
        • Schaich M.
        • Schetelig J.
        • Kiani A.
        • Ordemann R.
        • Ehninger G.
        • Schmitz M.
        • Bornhäuser M.
        Treatment of refractory acute GVHD with third-party MSC expanded in platelet lysate-containing medium.
        Bone Marrow Transplantation. 2008; 43: 245-251https://doi.org/10.1038/bmt.2008.316
        • Lucchini G.
        • Introna M.
        • Dander E.
        • Rovelli A.
        • Balduzzi A.
        • Bonanomi S.
        • Salvadè A.
        • Capelli C.
        • Belotti D.
        • Gaipa G.
        • Perseghin P.
        • Vinci P.
        • Lanino E.
        • Chiusolo P.
        • Orofino M.G.
        • Marktel S.
        • Golay J.
        • Rambaldi A.
        • Biondi A.
        • &Biagi E
        Platelet-lysate-expanded mesenchymal stromal cells as a salvage therapy for severe resistant graft-versus-host disease in a pediatric population.
        Biology of Blood and Marrow Transplantation. 2010; 16: 1293-1301https://doi.org/10.1016/j.bbmt.2010.03.017
        • Herrmann R.
        • Sturm M.
        • Shaw K.
        • Purtill D.
        • Cooney J.
        • Wright M.
        • Phillips M.
        • Cannell P.
        Mesenchymal stromal cell therapy for steroid-refractory acute and chronic graft versus host disease: a phase 1 study.
        International Journal of Hematology. 2012; 95: 182-188https://doi.org/10.1007/s12185-011-0989-2
        • Ball L.M.
        • Bernardo M.E.
        • Roelofs H.
        • van Tol M.J.D.
        • Contoli B.
        • Zwaginga J.J.
        • Avanzini M.A.
        • Conforti A.
        • Bertaina A.
        • Giorgiani G.
        • Jol-van Der Zijde C.M.
        • Zecca M.
        • le Blanc K.
        • Frassoni F.
        • Egeler R.M.
        • Fibbe W.E.
        • Lankester A.C.
        • Locatelli F.
        Multiple infusions of mesenchymal stromal cells induce sustained remission in children with steroid-refractory, grade III-IV acute graft-versus-host disease.
        British Journal of Haematology. 2013; 163: 501-509https://doi.org/10.1111/bjh.12545
        • Resnick I.B.
        • Barkats C.
        • Shapira M.Y.
        • Stepensky P.
        • Bloom A.I.
        • Shimoni A.
        Treatment of severe steroid resistant acute GVHD with mesenchymal stromal cells (MSC).
        Am J Blood Res. 2013; 3: 225-238
        • Sánchez-Guijo F.
        • Caballero-Velázquez T.
        • López-Villar O.
        • Redondo A.
        • Parody R.
        • Martínez C.
        • Olavarría E.
        • Andreu E.
        • Prósper F.
        • Díez-Campelo M.
        • Regidor C.
        • Villaron E.
        • López-Corral L.
        • Caballero D.
        • Cañizo M.C.D.
        • Pérez-Simon J.A.
        Sequential third-party mesenchymal stromal cell therapy for refractory acute graft-versus-host disease.
        Biology of Blood and Marrow Transplantation. 2014; 20: 1580-1585https://doi.org/10.1016/j.bbmt.2014.06.015
        • Muroi K.
        • Miyamura K.
        • Okada M.
        • Yamashita T.
        • Murata M.
        • Ishikawa T.
        • Uike N.
        • Hidaka M.
        • Kobayashi R.
        • Imamura M.
        • Tanaka J.
        • Ohashi K.
        • Taniguchi S.
        • Ikeda T.
        • Eto T.
        • Mori M.
        • Yamaoka M.
        • Ozawa K.
        Bone marrow-derived mesenchymal stem cells (JR-031) for steroid-refractory grade III or IV acute graft-versus-host disease: a phase II/III study.
        International Journal of Hematology. 2015; 103: 243-250https://doi.org/10.1007/s12185-015-1915-9
        • te Boome L.C.J.
        • Mansilla C.
        • van der Wagen L.E.
        • Lindemans C.A.
        • Petersen E.J.
        • Spierings E.
        • Thus K.A.
        • Westinga K.
        • Plantinga M.
        • Bierings M.
        • Broers A.E.C.
        • Cuijpers M.L.H.
        • van Imhoff G.W.
        • Janssen J.J.
        • Huisman C.
        • Zeerleder S.
        • Huls G.
        • Boelens J.J.
        • Wulffraat N.M.
        • Kuball J.
        Biomarker profiling of steroid-resistant acute GVHD in patients after infusion of mesenchymal stromal cells.
        Leukemia. 2015; 29: 1839-1846https://doi.org/10.1038/leu.2015.89
        • von Dalowski F.
        • Kramer M.
        • Wermke M.
        • Wehner R.
        • Röllig C.
        • Alakel N.
        • Stölzel F.
        • Parmentier S.
        • Sockel K.
        • Krech M.
        • Schmitz M.
        • Platzbecker U.
        • Schetelig J.
        • Bornhäuser M.
        • von Bonin M.
        Mesenchymal stromal cells for treatment of acute steroid-refractory graft versus host disease: clinical responses and long-term outcome.
        Stem Cells. 2015; 34: 357-366https://doi.org/10.1002/stem.2224
        • Jurado M.
        • de la Mata C.
        • Ruiz-García A.
        • López-Fernández E.
        • Espinosa O.
        • Remigia M.J.
        • Moratalla L.
        • Goterris R.
        • García-Martín P.
        • Ruiz-Cabello F.
        • Garzón S.
        • Pascual M.J.
        • Espigado I.
        • Solano C.
        Adipose tissue-derived mesenchymal stromal cells as part of therapy for chronic graft-versus-host disease: a phase I/II study.
        Cytotherapy. 2017; 19: 927-936https://doi.org/10.1016/j.jcyt.2017.05.002
        • Dotoli G.M.
        • de Santis G.C.
        • Orellana M.D.
        • de Lima Prata K.
        • Caruso S.R.
        • Fernandes T.R.
        • Rensi Colturato V.A.
        • Kondo A.T.
        • Hamerschlak N.
        • Simões B.P.
        • Covas D.T.
        Mesenchymal stromal cell infusion to treat steroid-refractory acute GVHD III/IV after hematopoietic stem cell transplantation.
        Bone Marrow Transplantation. 2017; 52: 859-862https://doi.org/10.1038/bmt.2017.35
        • Salmenniemi U.
        • Itälä-Remes M.
        • Nystedt J.
        • Putkonen M.
        • Niittyvuopio R.
        • Vettenranta K.
        • Korhonen M.
        Good responses but high TRM in adult patients after MSC therapy for GVHD.
        Bone Marrow Transplantation. 2016; 52: 606-608https://doi.org/10.1038/bmt.2016.317
        • Bonig H.
        • Kuçi Z.
        • Kuçi S.
        • Bakhtiar S.
        • Basu O.
        • Bug G.
        • Dennis M.
        • Greil J.
        • Barta A.
        • Kállay K.M.
        • Lang P.
        • Lucchini G.
        • Pol R.
        • Schulz A.
        • Sykora K.W.
        • Teichert Von Luettichau I.
        • Herter-Sprie G.
        • Ashab Uddin M.
        • Jenkin P.
        • Bader P.
        Children and adults with refractory acute graft-versus-host disease respond to treatment with the mesenchymal stromal cell preparation “MSC-FFM”—Outcome Report of 92 Patients.
        Cells. 2019; 8: 1577https://doi.org/10.3390/cells8121577
        • Kebriaei P.
        • Hayes J.
        • Daly A.
        • Uberti J.
        • Marks D.I.
        • Soiffer R.
        • Waller E.K.
        • Burke E.
        • Skerrett D.
        • Shpall E.
        • Martin P.J.
        A phase 3 randomized study of Remestemcel-L versus placebo added to second-line therapy in patients with steroid-refractory acute graft-versus-host disease.
        Biology of Blood and Marrow Transplantation. 2020; 26: 835-844https://doi.org/10.1016/j.bbmt.2019.08.029
        • Soder R.P.
        • Dawn B.
        • Weiss M.L.
        • Dunavin N.
        • Weir S.
        • Mitchell J.
        • Li M.
        • Shune L.
        • Singh A.K.
        • Ganguly S.
        • Morrison M.
        • Abdelhakim H.
        • Godwin A.K.
        • Abhyankar S.
        • McGuirk J.
        A phase I study to evaluate two doses of Wharton's jelly-derived mesenchymal stromal cells for the treatment of de novo high-risk or steroid-refractory acute graft versus host disease.
        Stem Cell Reviews and Reports. 2020; 16: 979-991https://doi.org/10.1007/s12015-020-10015-8
        • Purtill D.
        • Cirillo M.
        • Fogarty J.
        • Tan D.
        • Cooney J.
        • Wright M.
        • Cannell P.
        • Herrmann R.
        • Sturm M.
        Early cessation of a randomised study in acute graft versus host disease: upfront mesenchymal stromal cells with corticosteroids versus corticosteroids alone.
        Bone Marrow Transplantation. 2020; 55: 2199-2201https://doi.org/10.1038/s41409-020-0955-9
        • Boberg E.
        • Bahr L.
        • Afram G.
        • Lindström C.
        • Ljungman P.
        • Heldring N.
        • Petzelbauer P.
        • Garming Legert K.
        • Kadri N.
        • le Blanc K.
        Treatment of chronic GVHD with mesenchymal stromal cells induces durable responses: a phase II study.
        Stem Cells Translational Medicine. 2020; 9: 1190-1202https://doi.org/10.1002/sctm.20-0099
        • Bloor A.J.C.
        • Patel A.
        • Griffin J.E.
        • Gilleece M.H.
        • Radia R.
        • Yeung D.T.
        • Drier D.
        • Larson L.S.
        • Uenishi G.I.
        • Hei D.
        • Kelly K.
        • Slukvin I.
        • Rasko J.E.J.
        Production, safety and efficacy of iPSC-derived mesenchymal stromal cells in acute steroid-resistant graft versus host disease: a phase I, multicenter, open-label, dose-escalation study.
        Nature Medicine. 2020; 26: 1720-1725https://doi.org/10.1038/s41591-020-1050-x
        • Murata M.
        • Terakura S.
        • Wake A.
        • Miyao K.
        • Ikegame K.
        • Uchida N.
        • Kataoka K.
        • Miyamoto T.
        • Onizuka M.
        • Eto T.
        • Doki N.
        • Ota S.
        • Sato M.
        • Hashii Y.
        • Ichinohe T.
        • Fukuda T.
        • Atsuta Y.
        • Okamoto S.
        • Teshima T.
        Off-the-shelf bone marrow-derived mesenchymal stem cell treatment for acute graft-versus-host disease: real-world evidence.
        Bone Marrow Transplantation. 2021; 56: 2355-2366https://doi.org/10.1038/s41409-021-01304-y
        • Galipeau J.
        • Sensébé L.
        Mesenchymal stromal cells: clinical challenges and therapeutic opportunities.
        Cell Stem Cell. 2018; 22: 824-833https://doi.org/10.1016/j.stem.2018.05.004
        • van der Wagen L.E.
        • Miranda-Bedate A.
        • Janssen A.
        • Fernando F.
        • Appukudige N.
        • van Dooremalen S.
        • Westinga K.
        • Admiraal R.
        • Lorenowicz M.J.
        • Huls G.
        • Janssen J.J.
        • Broers A.E.
        • van der Velden W.J.
        • van Marwijk Kooy R.
        • Hazenberg M.D.
        • de Haar C.
        • Lindemans C.
        • Boelens J.
        • Kuball J.
        Efficacy of MSC for steroid-refractory acute GVHD associates with MSC donor age and a defined molecular profile.
        Bone Marrow Transplantation. 2020; 55: 2188-2192https://doi.org/10.1038/s41409-020-0910-9
        • Simonetta F.
        • Alvarez M.
        • Negrin R.S.
        Natural killer cells in graft-versus-host-disease after allogeneic hematopoietic cell transplantation.
        Frontiers in Immunology. 2017; 8https://doi.org/10.3389/fimmu.2017.00465
        • Zhang J.
        • Chen H.M.
        • Ma G.
        • Zhou Z.
        • Raulet D.
        • Rivera A.L.
        • Chen S.H.
        • Pan P.Y.
        The mechanistic study behind suppression of GVHD while retaining GVL activities by myeloid-derived suppressor cells.
        Leukemia. 2019; 33: 2078-2089https://doi.org/10.1038/s41375-01
        • Fan Q.
        • Liu H.
        • Liang X.
        • Yang T.
        • Fan Z.
        • Huang F.
        • Ling Y.
        • Liao X.
        • Xuan L.
        • Xu N.
        • Xu X.
        • Ye J.
        • Liu Q.
        Superior GVHD-free, relapse-free survival for G-BM to G-PBSC grafts is associated with higher MDSCs content in allografting for patients with acute leukemia.
        Journal of Hematology & Oncology. 2017; 10https://doi.org/10.1186/s13045-017-0503-2
        • Demosthenous C.
        • Sakellari I.
        • Douka V.
        • Papayanni P.G.
        • Anagnostopoulos A.
        • Gavriilaki E.
        The role of myeloid-derived suppressor cells (MDSCs) in graft-versus-host disease (GVHD).
        Journal of Clinical Medicine. 2021; 10: 2050https://doi.org/10.3390/jcm10102050
        • Cai X.
        • Zhang L.
        • Wei W.
        Regulatory B cells in inflammatory diseases and tumor.
        International Immunopharmacology. 2019; 67: 281-286https://doi.org/10.1016/j.intimp.2018.12.007
        • Hu Y.
        • He G.L.
        • Zhao X.Y.
        • Zhao X.S.
        • Wang Y.
        • Xu L.P.
        • Zhang X.H.
        • Yu X.Z.
        • Liu K.Y.
        • Chang Y.J.
        • Huang X.J.
        Regulatory B cells promote graft-versus-host disease prevention and maintain graft-versus-leukemia activity following allogeneic bone marrow transplantation.
        OncoImmunology. 2017; 6e1284721https://doi.org/10.1080/2162402x.2017.1284721
        • Ferrara J.L.
        • Levine J.E.
        • Reddy P.
        • Holler E.
        Graft-versus-host disease.
        The Lancet. 2009; 373: 1550-1561https://doi.org/10.1016/s0140-6736(09)60237-3
      2. CenterWatch RSS. Graft-versus-host-disease (GVHD) FDA approved drugs. Retrieved October 31, 2022, from https://www.centerwatch.com/directories/1067-fda-approved-drugs/topic/626-graft-versus-host-disease-gvhd.