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Bone Marrow Transplantation Platform to Investigate the Role of Dendritic Cells in Graft-versus-Host Disease
Published on: March 17, 2020
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Mesenchymal stem cells attenuate rat graft-versus-host disease
Masayuki Fujino1, Ping Zhu, Yusuke Kitazawa
1Division of Transplantation Immunology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
Methods in Molecular Biology (Clifton, N.J.)
|September 1, 2014
Summary
Mesenchymal stem cells (MSCs) show potential in treating T cell diseases. However, cloned MSCs unexpectedly enhanced T cell proliferation and did not improve graft-versus-host disease (GvHD) in a rat model.
Area of Science:
- Immunology
- Cell Biology
- Regenerative Medicine
Background:
- Mesenchymal stem cells (MSCs) possess potent immunoregulatory properties.
- Graft-versus-host disease (GvHD) is a significant complication following allogeneic hematopoietic stem cell transplantation (HSCT).
Purpose of the Study:
- To investigate the efficacy of MSCs in regulating GvHD.
- To compare the effects of conventionally cultured MSCs versus cloned MSCs on T cell proliferation and GvHD.
Main Methods:
- MSCs were isolated from Lewis rat bone marrow and cultured.
- Purification of MSCs and macrophages was performed using autoMACS.
- Cloned MSCs were generated via limiting dilution and expanded for over 6 months.
- Adoptive transfer of MSCs was used to treat a rat GvHD model.
Main Results:
- Cultured MSCs exhibited typical MSC morphology and immunophenotypes.
- Conventional MSCs regulated systemic GvHD in the rat model.
- Cloned MSCs enhanced T cell proliferation in vitro and did not improve GvHD incidence or severity.
Conclusions:
- Short-term cultured MSCs demonstrated immunosuppressive effects relevant to GvHD.
- Cloned MSCs displayed contrasting effects, enhancing T cell proliferation and failing to ameliorate GvHD.
- This study highlights significant differences in MSC regulatory effects based on culture and cloning methods.
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