Death and inflammation following somatic cell transplantation

被引:36
作者
Copland, Ian B. [1 ,2 ,3 ]
Galipeau, Jacques [2 ,3 ,4 ]
机构
[1] Emory Univ, Winship Canc Ctr, Atlanta, GA 30322 USA
[2] Emory Univ, Dept Hematol & Med Oncol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Atlanta, GA 30322 USA
[4] Emory Univ, Dept Pediat, Atlanta, GA 30322 USA
关键词
Programmed cell death; Apoptosis; Anoikis necrosis; Mesenchymal stem cell; Somatic cell; Transplantation; MESENCHYMAL STEM-CELLS; MARROW STROMAL CELLS; ANTIGEN-PRESENTING CELL; VERSUS-HOST-DISEASE; FETAL BOVINE SERUM; HUMAN BONE-MARROW; APOPTOTIC CELLS; IN-VITRO; MYOCARDIAL-INFARCTION; GENE-THERAPY;
D O I
10.1007/s00281-011-0274-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The fields of regenerative medicine and cellular therapy have been the subject of tremendous hype and hope. In particular, the perceived usage of somatic cells like mesenchymal stromal stem cells (MSCs) has captured the imagination of many. Clinical trials are currently evaluating the therapeutic efficacy of MSCs in disorders ranging from heart disease to pediatric graft-vs-host disease; however, numerous questions still remain regarding mechanism of action, effective dose, and whether these cells can be used in the allogeneic setting. One of the major issues surrounding the development of somatic cell therapies like MSCs is that despite evoking a positive response, long-term engraftment and persistence of these cells is rare. Consequently, very large cell doses need be administered raising production, delivery, and efficacy issues. In this review, we will discuss causes for this lack of persistence and highlight some of the methodologies be used to enhance cell survival post-transplantation.
引用
收藏
页码:535 / 550
页数:16
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