Is xenotransplantation of embryonic stem cells a realistic option?

被引:13
作者
Bonnevie, Lionel
Bel, Alain
Sabbah, Laurent
Al Attar, Nawwar
Pradeau, Pascal
Weill, Bernard
Le Deist, Francoise
Bellamy, Valerie
Peyrard, Severine
Menard, Claudine
Desnos, Michel
Bruneval, Patrick
Binder, Patrice
Hagege, Albert A.
Puceat, Michel
Menasche, Philippe [1 ]
机构
[1] Univ Paris 05, Hop Europeen Georges Pompidou, Assistance Publ Hop Paris, Fac Med,INSERM,U633,Dept Cardiol, F-75270 Paris 06, France
[2] Hop Instruct Armeees Begin, Dept Cardiol, St Mande, France
[3] Hop Europeen Georges Pompidou, Assistance Publ Hop Paris, Dept Cardiovasc Surg, Paris, France
[4] INSERM, U 633, Paris, France
[5] IMASSA, Bretigny Sur Orge, France
[6] Univ Paris 05, Hop Cochin, Assistance Publ Hop Paris, Lab Immunol,IFR Alfred Jost,EA 1833, F-75270 Paris 06, France
[7] Univ Montreal, Dept Immunol & Microbiol, Montreal, PQ H3C 3J7, Canada
[8] Hop Europeen Georges Pompidou, Assistance Publ Hop Paris, Clin Invest Ctr, INSERM, Paris, France
[9] CNRS, CRBM, F-34033 Montpellier, France
[10] CNRS, Ctr Rech Biochim Macromol, F-75700 Paris, France
[11] Univ Paris 05, Hop Europeen Georges Pompidou, Assistance Publ Hop Paris, Dept Pathol, F-75270 Paris 06, France
[12] INSERM, U652, Paris, France
[13] Genethon, ISTEM, Evry, France
[14] INSERM, U 421, Evry, France
关键词
embryonic stem cells; myocardial infarction; xenotransplantation; cardiac cell therapy;
D O I
10.1097/01.tp.0000247798.68218.29
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To test the purported immune privilege of embryonic stem cells (ESC) in the challenging setting of xenotransplantation, 14 immunocompetent baboons were subjected to a coronary artery occlusion-reperfusion sequence and, two weeks later, randomized to receive in-scar injections of culture medium or cardiac-committed mouse ESC engineered to express fluorescent reporter genes driven by cardiac-specific promoters. Two months after transplantation, left ventricular function, as assessed by echocardiography, deteriorated to a similar extent in control and treated baboons. This correlated with failure to identify the grafted cells by X-gal histology and immunofluorescence. Rejection did not seem to be mediated by xenoantibodies, but rather by T lymphocytes and natural killer cells as suggested by positive immunostaining for CD3 and CD56 early after transplantation. There was no increase in circulating levels of regulatory T cells. These data raise a cautionary note about the immune privilege of ESC and suggest that from a mere immunologic standpoint, ESC xenotransplantation is likely to be an unrealistic challenge.
引用
收藏
页码:333 / 335
页数:3
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