Analysis of Tissues Following Mesenchymal Stromal Cell Therapy in Humans Indicates Limited Long-Term Engraftment and No Ectopic Tissue Formation

被引:446
作者
von Bahr, L. [1 ,2 ]
Batsis, I. [4 ,5 ]
Moll, G. [2 ]
Hagg, M. [2 ]
Szakos, A. [3 ]
Sundberg, B. [2 ]
Uzunel, M. [2 ]
Ringden, O. [2 ]
Le Blanc, K. [1 ,2 ]
机构
[1] Karolinska Univ Hosp, Hematol Ctr, SE-14186 Stockholm, Sweden
[2] Karolinska Inst, Dept Lab Med, Div Clin Immunol & Transfus Med, Stockholm, Sweden
[3] Karolinska Inst, Dept Lab Med, Div Pathol, Stockholm, Sweden
[4] George Papanicolaou Hosp, Dept Hematol, Thessaloniki, Greece
[5] George Papanicolaou Hosp, HCT Unit, Thessaloniki, Greece
基金
瑞典研究理事会;
关键词
Mesenchymal stromal cells; Cell transplantation; Humans; Polymerase chain reaction; Graft survival; STEM-CELLS; BONE-MARROW; MYOCARDIAL-INFARCTION; FUSION; TRANSFORMATION; IRRADIATION; INFUSION; REPAIR; MSC;
D O I
10.1002/stem.1118
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stromal cells (MSCs) are explored as a novel treatment for a variety of medical conditions. Their fate after infusion is unclear, and long-term safety regarding malignant transformation and ectopic tissue formation has not been addressed in patients. We examined autopsy material from 18 patients who had received human leukocyte antigen (HLA)-mismatched MSCs, and 108 tissue samples from 15 patients were examined by PCR. No signs of ectopic tissue formation or malignant tumors of MSC-donor origin were found on macroscopic or histological examination. MSC donor DNA was detected in one or several tissues including lungs, lymph nodes, and intestine in eight patients at levels from 1/100 to < 1/1,000. Detection of MSC donor DNA was negatively correlated with time from infusion to sample collection, as DNA was detected from nine of 13 MSC infusions given within 50 days before sampling but from only two of eight infusions given earlier. There was no correlation between MSC engraftment and treatment response. We conclude that MSCs appear to mediate their function through a "hit and run" mechanism. The lack of sustained engraftment limits the long-term risks of MSC therapy. STEM CELLS 2012;30:1575-1578
引用
收藏
页码:1575 / 1578
页数:4
相关论文
共 22 条
[1]   Quantitative assessment of hematopoietic chimerism after bone marrow transplantation by real-time quantitative polymerase chain reaction [J].
Alizadeh, M ;
Bernard, M ;
Danic, B ;
Dauriac, C ;
Birebent, B ;
Lapart, C ;
Lamy, T ;
Le Prisé, PY ;
Beauplet, A ;
Bories, D ;
Semana, G ;
Quelvennec, E .
BLOOD, 2002, 99 (12) :4618-4625
[2]   Mesenchymal stem cells distribute to a wide range of tissues following systemic infusion into nonhuman primates [J].
Devine, SM ;
Cobbs, C ;
Jennings, M ;
Bartholomew, A ;
Hoffman, R .
BLOOD, 2003, 101 (08) :2999-3001
[3]   Engraftment of allogeneic mesenchymal stem cells in the bone marrow of a patient with severe idiopathic aplastic anemia improves stroma [J].
Fouillard, L ;
Bensidhoum, M ;
Bories, D ;
Bonte, H ;
Lopez, M ;
Moseley, AM ;
Smith, A ;
Lesage, S ;
Beaujean, F ;
Thierry, D ;
Gourmelon, P ;
Najman, A ;
Gorin, NC .
LEUKEMIA, 2003, 17 (02) :474-476
[4]   Local irradiation not only induces homing of human mesenchymal stem cells at exposed sites but promotes their widespread engraftment to multiple organs:: A study of their quantitative distribution after irradiation damage [J].
Francois, Sabine ;
Bensidhoum, Morad ;
Mouiseddine, Moubarak ;
Mazurier, Christelle ;
Allenet, Benedicte ;
Semont, Alexandra ;
Frick, Johanna ;
Sache, Aniandine ;
Bouchet, Sandrine ;
Thierry, Dominique ;
Goumelon, Patrick ;
Gorin, Norbert-Claude ;
Chapel, Alain .
STEM CELLS, 2006, 24 (04) :1020-1029
[5]   Clarification of the nomenclature for MSC: The international society for cellular therapy position statement [J].
Horwitz, EM ;
Le Blanc, K ;
Dominici, M ;
Mueller, I ;
Slaper-Cortenbach, I ;
Marini, FC ;
Deans, RJ ;
Krause, DS ;
Keating, A .
CYTOTHERAPY, 2005, 7 (05) :393-395
[6]   Cell-dose-dependent increases in circulating levels of immune effector cells in rhesus macaques following intracranial injection of allogeneic MSCs [J].
Isakova, Iryna A. ;
Dufour, Jason ;
Lanclos, Calvin ;
Bruhn, Julie ;
Phinney, Donald G. .
EXPERIMENTAL HEMATOLOGY, 2010, 38 (10) :957-967
[7]   Extensive fusion of haematopoietic cells with Purkinje neurons in response to chronic inflammation [J].
Johansson, Clas B. ;
Youssef, Sawsan ;
Koleckar, Kassie ;
Holbrook, Colin ;
Doyonnas, Regis ;
Corbel, Stephane Y. ;
Steinman, Lawrence ;
Rossi, Fabio M. V. ;
Blau, Helen M. .
NATURE CELL BIOLOGY, 2008, 10 (05) :575-583
[8]   Allogeneic mesenchymal stem cell infusion for treatment of metachromatic leukodystrophy (MLD) and Hurler syndrome (MPS-IH) [J].
Koç, ON ;
Day, J ;
Nieder, M ;
Gerson, SL ;
Lazarus, HM ;
Krivit, W .
BONE MARROW TRANSPLANTATION, 2002, 30 (04) :215-222
[9]   Rapid hematopoietic recovery after coinfusion of autologous-blood stem cells and culture-expanded marrow mesenchymal stem cells in advanced breast cancer patients receiving high-dose chemotherapy [J].
Koç, ON ;
Gerson, SL ;
Cooper, BW ;
Dyhouse, SM ;
Haynesworth, SE ;
Caplan, AI ;
Lazarus, HM .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (02) :307-316
[10]   Dynamic imaging of allogeneic mesenchymal stem cells trafficking to myocardial infarction [J].
Kraitchman, DL ;
Tatsumi, M ;
Gilson, WD ;
Ishimori, T ;
Kedziorek, D ;
Walczak, P ;
Segars, P ;
Chen, HH ;
Fritzges, D ;
Izbudak, I ;
Young, RG ;
Marcelino, M ;
Pittenger, MF ;
Solaiyappan, M ;
Boston, RC ;
Tsui, BMW ;
Wahl, RL ;
Bulte, JWM .
CIRCULATION, 2005, 112 (10) :1451-1461