Mesenchymal stem cells for treatment of steroid-resistant, severe, acute graft-versus-host disease:: a phase II study

被引:2062
作者
LeBlanc, Katarina [1 ,2 ]
Frassoni, Francesco [3 ,4 ]
Ball, Lynne [6 ]
Locatelli, Franco [8 ]
Roelofs, Helene [7 ]
Lewis, Ian [9 ]
Lanino, Edoardo [5 ]
Sundberg, Berit [1 ,2 ]
Bernardo, Maria Ester [8 ]
Remberger, Mats [1 ,2 ]
Dini, Giorgio [5 ]
Egeler, R. Maarten [6 ]
Bacigalupo, Andrea [3 ,4 ]
Fibbe, Willem [7 ]
Ringden, Olle [1 ,2 ]
机构
[1] Karolinska Univ Hosp, Haematol Ctr, Stockholm, Sweden
[2] Karolinska Univ Hosp, Ctr Allogen Stem Cell Transplantat, Div Clin Immunol, Stockholm, Sweden
[3] Osped San Martino Genova, Ctr Cellule Staminali & Terapia Cellulare, Genoa, Italy
[4] Osped San Martino Genova, Div Ematol, Genoa, Italy
[5] IRCCS G Gaslini, Dipartimento Ematol & Oncol, Genoa, Italy
[6] Leiden Univ, Med Ctr, Dept Paediat, Leiden, Netherlands
[7] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Transfus, Leiden, Netherlands
[8] Univ Pavia, Oncoematol Pediat, Fdn IRCCS Policlin San Matteo, I-27100 Pavia, Italy
[9] Inst Med & Vet Sci, Div Haematol, Adelaide, SA 5000, Australia
关键词
D O I
10.1016/S0140-6736(08)60690-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Severe graft-versus-host disease (GVHD) is a life-threatening complication after allogeneic transplantation with haemopoietic stem cells. Mesenchymal stem cells modulate immune responses in vitro and in vivo. We aimed to assess whether mesenchymal stem cells could ameliorate GVHD after haemopoietic-stem-cell transplantation. Methods Patients with steroid-resistant, severe, acute GVHD were treated with mesenchymal stem cells, derived with the European Group for Blood and Marrow Transplantation ex-vivo expansion procedure, in a multicentre, phase II experimental study. We recorded response, transplantation-related deaths, and other adverse events for up to 60 months' follow-up from infusion of the cells. Findings Between October, 2001, and January, 2007, 55 patients were treated. The median dose of bone-marrow derived mesenchymal stem cells was 1.4x10(6) (Min-max range 0.4-9x10(6)) cells per kg bodyweight. 27 patients received one dose, 22 received two doses, and six three to five doses of cells obtained from HLA-identical sibling donors (n=5), haploidentical donors (n=18), and third-party HLA-mismatched donors (n=69). 30 patients had a complete response and nine showed improvement. No patients had side-effects during or immediately after infusions of mesenchymal stem cells. Response rate was not related to donor HLA-match. Three patients had recurrent malignant disease and one developed de-novo acute myeloid leukaemia of recipient origin. Complete responders had lower transplantation-related mortality 1 year after infusion than did patients with partial or no response (11 [37%] of 30 vs 18 [72%] of 25; p=0.002) and higher overall survival 2 years after haemopoietic-stem-cell transplantation (16 [53%] of 30 vs four [16%] of 25; p=0 . 018). Interpretation Infusion of mesenchymal stem cells expanded in vitro, irrespective of the donor, might be an effective therapy for patients with steroid-resistant, acute GVHD. Funding Swedish Cancer Society Children's Cancer Foundation, Swedish Research Council, Cancer Society in Stockholm, Cancer and Allergy Foundation, Karolinska. Institutet, Istituto Superiore di Sanita, European Union, Regione Lombardia, Fondazione CARIPLO, Associazione Italiana Ricerca contro il Cancro, Compagnia di San Paolo Torino, Progetto CARIGE Cellule Staminali, European Commission, Ministero dell'Universita e della Ricerca Scientifica e Tecnologica, Ricerca Finalizzata Regione Liguria 2005 Assistenza Domiciliare, Dutch Programme for Tissue Engineering.
引用
收藏
页码:1579 / 1586
页数:8
相关论文
共 31 条
[1]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]   Cotransplantation of ex vivo-expanded mesenchymal stem cells accelerates lymphocyte recovery and may reduce the risk of graft failure in haploidentical hematopoietic stem-cell transplantation [J].
Ball, Lynne M. ;
Bernardo, Maria Ester ;
Roelofs, Helene ;
Lankester, Arjan ;
Cometa, Angela ;
Egeler, R. Maarten ;
Locatelli, Franco ;
Fibbe, Willem E. .
BLOOD, 2007, 110 (07) :2764-2767
[3]   Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo [J].
Bartholomew, A ;
Sturgeon, C ;
Siatskas, M ;
Ferrer, K ;
McIntosh, K ;
Patil, S ;
Hardy, W ;
Devine, S ;
Ucker, D ;
Deans, R ;
Moseley, A ;
Hoffman, R .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (01) :42-48
[4]  
Blume KG, 2004, THOMAS HEMATOPOIETIC
[5]   How I treat refractory acute GVHD [J].
Deeg, H. Joachim .
BLOOD, 2007, 109 (10) :4119-4126
[6]   A proportional hazards model for the subdistribution of a competing risk [J].
Fine, JP ;
Gray, RJ .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1999, 94 (446) :496-509
[7]   HETEROTOPIC TRANSPLANTS OF BONE MARROW - ANALYSIS OF PRECURSOR CELLS FOR OSTEOGENIC AND HEMATOPOIETIC TISSUES [J].
FRIEDENSTEIN, AJ ;
PETRAKOVA, KV ;
KUROLESOVA, AI ;
FROLOVA, GP .
TRANSPLANTATION, 1968, 6 (02) :230-+
[8]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304
[9]  
GOLDMAN JM, 1982, LANCET, V2, P623
[10]  
Gooley TA, 1999, STAT MED, V18, P695, DOI 10.1002/(SICI)1097-0258(19990330)18:6<695::AID-SIM60>3.3.CO