Paolo F Caimi1, Jane Reese, Zhenghong Lee, Hillard M Lazarus. 1. Department of Medicine, Case Western Reserve University, Case Comprehensive Cancer Center, University Hospitals Case Medical Center, Cleveland, Ohio 44106, USA.
Abstract
PURPOSE OF REVIEW: Multipotent mesenchymal stromal cells (MSCs) are rare cells resident in bone marrow and other organs capable of differentiating into mesodermal lineage tissues. MSCs possess immunomodulatory properties and have extensive capacity for ex-vivo expansion. Early clinical studies demonstrated safety and feasibility of infusing autologous MSCs and suggested a role in enhancing engraftment after hematopoietic cell transplant (HCT). Subsequent pilot studies using allogeneic MSCs showed safety but presented contradictory results regarding efficacy in treating graft-versus-host disease (GVHD). RECENT FINDINGS: Larger, phase II allogeneic MSC infusion studies, including cells obtained from haploidentical and third-party donors, showed efficacy in GVHD treatment; however, recent randomized, placebo-controlled studies failed to corroborate these results. New investigations include MSC infusions in umbilical cord blood transplantation, MSC therapy for tissue regeneration/repair, harvest and use of MSCs from adipose tissue and cell-tracking/imaging studies using radionuclides, gene and fluorescent dye-labeled MSCs. SUMMARY: MSCs remain the subject of intense investigation in HCT because of their differentiation potential and immunomodulatory properties. Whereas infusions of autologous, allogeneic and third-party donor MSCs are well tolerated, further research is needed to clarify the optimal methods for harvesting and expansion, optimal timing of administration and efficacy in the setting of HCT.
PURPOSE OF REVIEW: Multipotent mesenchymal stromal cells (MSCs) are rare cells resident in bone marrow and other organs capable of differentiating into mesodermal lineage tissues. MSCs possess immunomodulatory properties and have extensive capacity for ex-vivo expansion. Early clinical studies demonstrated safety and feasibility of infusing autologous MSCs and suggested a role in enhancing engraftment after hematopoietic cell transplant (HCT). Subsequent pilot studies using allogeneic MSCs showed safety but presented contradictory results regarding efficacy in treating graft-versus-host disease (GVHD). RECENT FINDINGS: Larger, phase II allogeneic MSC infusion studies, including cells obtained from haploidentical and third-party donors, showed efficacy in GVHD treatment; however, recent randomized, placebo-controlled studies failed to corroborate these results. New investigations include MSC infusions in umbilical cord blood transplantation, MSC therapy for tissue regeneration/repair, harvest and use of MSCs from adipose tissue and cell-tracking/imaging studies using radionuclides, gene and fluorescent dye-labeled MSCs. SUMMARY: MSCs remain the subject of intense investigation in HCT because of their differentiation potential and immunomodulatory properties. Whereas infusions of autologous, allogeneic and third-party donor MSCs are well tolerated, further research is needed to clarify the optimal methods for harvesting and expansion, optimal timing of administration and efficacy in the setting of HCT.
Authors: Karissa T Chabner; Gregor B Adams; Jianhua Qiu; Michael Moskowitz; Emily S Marsters; George P Topulos; David T Scadden Journal: Blood Date: 2004-06-15 Impact factor: 22.113
Authors: Jakub Tolar; Matthew J O'shaughnessy; Angela Panoskaltsis-Mortari; Ron T McElmurry; Scott Bell; Megan Riddle; R Scott McIvor; Stephen R Yant; Mark A Kay; Diane Krause; Catherine M Verfaillie; Bruce R Blazar Journal: Blood Date: 2006-01-12 Impact factor: 22.113
Authors: I Müller; S Kordowich; C Holzwarth; C Spano; G Isensee; A Staiber; S Viebahn; F Gieseke; H Langer; M P Gawaz; E M Horwitz; P Conte; R Handgretinger; M Dominici Journal: Cytotherapy Date: 2006 Impact factor: 5.414
Authors: Bing Ma; Kurt D Hankenson; James E Dennis; Arnold I Caplan; Steven A Goldstein; Michael R Kilbourn Journal: Nucl Med Biol Date: 2005-10 Impact factor: 2.408
Authors: Sophie E Boddington; Elizabeth J Sutton; Tobias D Henning; Alexander J Nedopil; Barbara Sennino; Anne Kim; Heike E Daldrup-Link Journal: Mol Imaging Biol Date: 2011-02 Impact factor: 3.488
Authors: Min Zhao; Patrick C Sachs; Xu Wang; Catherine I Dumur; Michael O Idowu; Valentina Robila; Michael P Francis; Joy Ware; Matthew Beckman; Aylin Rizki; Shawn E Holt; Lynne W Elmore Journal: Cancer Biol Ther Date: 2012-06-06 Impact factor: 4.742
Authors: Jeffery J Auletta; Amelia M Bartholomew; Richard T Maziarz; Robert J Deans; Robert H Miller; Hillard M Lazarus; Jeffrey A Cohen Journal: Immunotherapy Date: 2012-05 Impact factor: 4.196
Authors: Jorge Paz Rodriguez; Michael P Murphy; Soonjun Hong; Marialaura Madrigal; Keith L March; Boris Minev; Robert J Harman; Chien-Shing Chen; Ruben Berrocal Timmons; Annette M Marleau; Neil H Riordan Journal: Int Arch Med Date: 2012-02-08
Authors: Morgan T Sutton; David Fletcher; Nicole Episalla; Lauren Auster; Sukhmani Kaur; Mary Chandler Gwin; Michael Folz; Dante Velasquez; Varun Roy; Rolf van Heeckeren; Donald P Lennon; Arnold I Caplan; Tracey L Bonfield Journal: J Stem Cell Res Ther Date: 2017-09-22
Authors: J M Sempere; P Martinez-Peinado; M I Arribas; J A Reig; M L De La Sen; J J Zubcoff; M F Fraga; A F Fernández; A Santana; E Roche Journal: Clin Exp Immunol Date: 2014-05 Impact factor: 4.330