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Intravascular Mesenchymal Stromal/Stem Cell Therapy Product Diversification: Time for New Clinical Guidelines

期刊

TRENDS IN MOLECULAR MEDICINE
卷 25, 期 2, 页码 149-163

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ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2018.12.006

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资金

  1. German Research Foundation (DFG)
  2. German Federal Ministry of Education and Research (BMBF) through the BSRT [GSC203]
  3. BCRT
  4. BMBF (DIMEOS) [01EC1402B]
  5. DFG [FOR2165, GE2512/2-2]
  6. EU Horizon 2020 Research and Innovation Programme [733006, 779293]
  7. Fraternal Order of Eagles Diabetes Research Center
  8. Straub Foundation
  9. Swedish Research Council [K2014-64X-05971-34-4]
  10. Swedish Cancer Society [CAN2013/671]
  11. Cancer Society in Stockholm [111293]
  12. Karolinska Institutet
  13. H2020 Societal Challenges Programme [733006, 779293] Funding Source: H2020 Societal Challenges Programme

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Intravascular infusion is the most popular route for therapeutic multipotent mesenchymal stromal/stem cell (MSC) delivery in hundreds of clinical trials. Meta-analysis has demonstrated that bone marrow MSC infusion is safe. It is not clear if this also applies to diverse new cell products derived from other sources, such as adipose and perinatal tissues. Different MSC products display varying levels of highly procoagulant tissue factor (TF) and may adversely trigger the instant blood-mediated inflammatory reaction (IBMIR). Suitable strategies for assessing and controlling hemocompatibility and optimized cell delivery are crucial for the development of safer and more effective MSC therapies.

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