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Updated: May 2, 2026

Assessment of the Immunomodulatory Properties of Human Mesenchymal Stem Cells MSCs
Published on: December 24, 2015
Mesenchymal stem cells: immune evasive, not immune privileged
James A Ankrum1, Joon Faii Ong2, Jeffrey M Karp3
11] Center for Biomedical Engineering, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA. [2] Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Mesenchymal stem/stromal cells (MSCs) show promise for inflammatory conditions. However, their perceived immune privilege is challenged by immune rejection, raising questions about allogeneic MSC therapy efficacy and the need for strategies to enhance MSC persistence.
Area of Science:
- Immunology
- Cell Therapy
Background:
- Mesenchymal stem/stromal cells (MSCs) possess immunomodulatory properties beneficial for treating inflammatory diseases.
- MSCs were traditionally considered immune privileged, facilitating allogeneic transplantation and off-the-shelf therapies.
- Recent findings indicate potential immune rejection of allogeneic MSCs, challenging the immune privilege concept.
Purpose of the Study:
- To investigate the immune privilege status of MSCs.
- To explore the impact of MSC immune rejection on allogeneic therapy efficacy.
- To determine if strategies enhancing MSC persistence improve clinical outcomes.
Main Methods:
- Review of recent studies on MSC immunogenicity and immune rejection.
- Analysis of clinical data regarding autologous versus allogeneic MSC therapy outcomes.
- Evaluation of the 'hit and run' mechanism versus prolonged MSC persistence.
Main Results:
- Evidence suggests MSCs may not be completely immune privileged, as antibodies and rejection of allogeneic MSCs have been observed.
- The influence of donor MSC rejection on therapeutic efficacy remains unclear.
- No definitive clinical advantage of autologous over allogeneic MSCs has been established.
Conclusions:
- The immune privilege of MSCs is questionable, necessitating further research into immune responses against allogeneic MSCs.
- Strategies to protect MSCs from immune detection and prolong their in vivo persistence may enhance therapeutic efficacy.
- Improving MSC persistence could prevent patient sensitization to donor antigens and optimize treatment outcomes.
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