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Feeder-free Derivation of Neural Crest Progenitor Cells from Human Pluripotent Stem Cells
Published on: May 22, 2014
Human iPSC-Derived Neural Crest Stem Cells Exhibit Low Immunogenicity.
Vera J Mehler1,2, Chris J Burns1, Hans Stauss2
1Endocrinology Section, Biotherapeutics, National Institute for Biological Standards and Control (NIBSC), Blanche Lane, Potters Bar EN6 3QG, UK.
Induced pluripotent stem cell-derived neural crest stem cells (iPSC-NCSCs) show low immunogenicity, a crucial factor for their use in regenerative medicine. These cells did not trigger immune responses in mixed lymphocyte reactions, suggesting potential for safe cellular therapy.
Area of Science:
- Regenerative Medicine
- Immunology
- Stem Cell Biology
Background:
- Induced pluripotent stem cells (iPSCs) are being evaluated for cellular therapy.
- Allogeneic iPSC use requires safety evaluation, including immunogenicity assessment.
- IPSC-derived neural crest stem cells (iPSC-NCSCs) have therapeutic potential but their immunogenicity is unstudied.
Purpose of the Study:
- To assess the immunogenicity of iPSC-NCSCs for potential cellular therapy.
- To evaluate the expression of immune-related antigens and co-stimulatory molecules on iPSC-NCSCs.
- To investigate the functional immune response to iPSC-NCSCs using a mixed lymphocyte reaction.
Main Methods:
- Assessed human leukocyte antigen (HLA) class I and II expression on iPSC-NCSCs.
- Measured co-stimulatory molecule expression on iPSC-NCSCs.
- Conducted one-way mixed lymphocyte reactions with iPSC-NCSCs as stimulator cells.
Main Results:
- iPSC-NCSCs exhibited a non-immunogenic molecular phenotype.
- No detectable proliferation of CD3+ or CD3+CD8+ T cells was observed.
- No significant cytokine production was induced by iPSC-NCSCs.
Conclusions:
- iPSC-NCSCs demonstrate a lack of immunogenicity in vitro.
- The non-immunogenic profile supports the potential use of iPSC-NCSCs in regenerative medicine.
- Further research into iPSC-NCSC safety and efficacy for cellular therapy is warranted.
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