HSCT Recipients Have Specific Tolerance to MSC but not to the MSC Donor

被引:43
作者
Sundin, Mikael [1 ]
Barrett, A. John [5 ]
Ringden, Olle [1 ,3 ]
Uzunel, Mehmet [1 ]
Lonnies, Helena [1 ]
Dackland, Asa-Lena [2 ]
Christensson, Birger [2 ]
Le Blanc, Katarina [1 ,4 ]
机构
[1] Karolinska Inst, Dept Lab Med, Div Clin Immunol & Transfus Med, S-10401 Stockholm, Sweden
[2] Karolinska Inst, Div Pathol, Dept Lab Med, S-10401 Stockholm, Sweden
[3] Karolinska Univ Hosp, Ctr Allogene Stem Cell Transplantat, SE-14186 Stockholm, Sweden
[4] Karolinska Univ Hosp, Hematol Ctr, SE-14186 Stockholm, Sweden
[5] NIH, Allogene Stem Cell Transplant Sect, Hematol Branch, Bethesda, MD 20892 USA
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
immunogenicity; HLA-match; stem cell transplantation; mesenchymal stromal cells; MESENCHYMAL STEM-CELLS; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; IN-UTERO TRANSPLANTATION; STROMAL CELLS; ENGRAFTMENT; INHIBIT; RESPONSES; DIFFERENTIATION; PROLIFERATION;
D O I
10.1097/CJI.0b013e3181ab1807
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multipotent mesenchymal stromal cells (MSC) are increasingly used to treat refractory graft-versus-host-disease and other complications after hematopoietic stern cell transplantation (HSCT). We evaluated immunogenicity of HLA-mismatched MSC infused post transplant to HSCT recipients. Recipient lymphocyte response to MSC and peripheral blood lymphocytes (PBL) from the MSC or third party donors wits measured before and after infusion. In vitro primary and rechallenge lymphocyte responses of healthy individuals to MSC and to PBL from the MSC donor were similarly Studied. HSCT recipients given MSC responded to third party allostimuli, but showed no response to infused MSC before and upto 6 months after infusion, whereas maintaining an alloresponse to the MSC donor. This indicates immune unresponsiveness restricted to MSC, its the HSCT recipient was not tolerized to the MSC donor. In vitro, we confirmed that MSC failed to prime responder lymphocytes to rechallenge with PBL from the MSC donor, and lymphocytes primed with MSC donor and rechallenged with MSC only showed weak responses at high stimulator-responder ratios. Although MSC up-regulated lymphocyte gene expression of CD25, IFN-gamma, FoxP3, CTLA-4, and IL-10, they failed in both unprimed and primed responders to induce CD25 (activated) or CD57(+) (effector) CD4(+) or CD8(+) T-lymphocyte Subsets and only inconsistently induced FoxP3+ regulatory T-lymphocytes. These results show for the first time that infused MSC are only weakly immunogenic in humans and validate the clinical use of MSC from HLA-mismatched donors.
引用
收藏
页码:755 / 764
页数:10
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