Clinical Implication of Allogenic Implantation of Adipogenic Differentiated Adipose-Derived Stem Cells

  • Kim I
  • Bang S
  • Lee S
  • et al.
40Citations
Citations of this article
42Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

We recently reported that autologous adipogenic differentiated adipose-derived stem cells (ASCs) can potentially be used as an effective and safe therapy for soft-tissue regeneration. In the present study, we investigated whether adipogenic differentiated ASCs can be used for allogenic applications to enlarge their therapeutic use. The allogenic immune response of adipogenic differentiated ASCs was investigated by flow cytometry and mixed lymphocyte culture. To determine whether adipogenic differentiated ASCs can form new adipose tissue without immune rejection, these cells were implanted subcutaneously into allo- or xenogenic recipient mice. In addition, the safety of the allogenic implantation of adipogenic differentiated ASCs was explored in a phase I clinical study. Adipogenic differentiated ASCs do not express major histocompatibility complex (MHC) class II molecules and costimulatory molecules, and the expression levels of MHC class I decreased after differentiation. In addition, these cells do not elicit an immune response against MHC-mismatched allogenic lymphocytes and formed new adipose tissue without immune rejection in the subcutaneous region of MHC-mismatched mice. Moreover, these cells did not induce clinically significant local and systemic immune responses or adverse events in the subcutaneous region of donor-independent healthy subjects. These results suggest that adipogenic differentiated ASCs can be used as a “universal donor” for soft-tissue engineering in MHC-mismatched recipients.

Cite

CITATION STYLE

APA

Kim, I., Bang, S. I., Lee, S. K., Park, S. Y., Kim, M., & Ha, H. (2014). Clinical Implication of Allogenic Implantation of Adipogenic Differentiated Adipose-Derived Stem Cells. Stem Cells Translational Medicine, 3(11), 1312–1321. https://doi.org/10.5966/sctm.2014-0109

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free