Similar effect of autologous and allogeneic cell therapy for ischemic heart disease: systematic review and meta-analysis of large animal studies.

نویسندگان

  • Sanne Johanna Jansen Of Lorkeers
  • Joep Egbert Coenraad Eding
  • Hanna Mikaela Vesterinen
  • Tycho Ids Gijsbert van der Spoel
  • Emily Shamiso Sena
  • Henricus Johannes Duckers
  • Pieter Adrianus Doevendans
  • Malcolm Robert Macleod
  • Steven Anton Jozef Chamuleau
چکیده

RATIONALE In regenerative therapy for ischemic heart disease, use of both autologous and allogeneic stem cells has been investigated. Autologous cell can be applied without immunosuppression, but availability is restricted, and cells have been exposed to risk factors and aging. Allogeneic cell therapy enables preoperative production of potent cell lines and immediate availability of cell products, allowing off-the-shelf therapy. It is unknown which cell source is preferred with regard to improving cardiac function. OBJECTIVE We performed a meta-analysis of preclinical data of cell therapy for ischemic heart disease. METHODS AND RESULTS We conducted a systematic literature search to identify publications describing controlled preclinical trials of unmodified stem cell therapy in large animal models of myocardial ischemia. Data from 82 studies involving 1415 animals showed a significant improvement in mean left ventricular ejection fraction in treated compared with control animals (8.3%, 95% confidence interval, 7.1-9.5; P<0.001). Meta-regression revealed a similar difference in left ventricular ejection fraction in autologous (8.8%, 95% confidence interval, 7.3-10.3; n=981) and allogeneic (7.3%, 95% confidence interval, 4.4-10.2, n=331; P=0.3) cell therapies. CONCLUSIONS Autologous and allogeneic cell therapy for ischemic heart disease show a similar improvement in left ventricular ejection fraction in large animal models of myocardial ischemia, compared with placebo. These results are important for the design of future clinical trials.

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عنوان ژورنال:
  • Circulation research

دوره 116 1  شماره 

صفحات  -

تاریخ انتشار 2015