Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8463540 | Cellular Immunology | 2018 | 21 Pages |
Abstract
Putative monocytic myeloid-derived suppressor cells (mMDSC; lineageâHLA-DRâ/lo) were generated in 7-day cultures from normal rhesus macaque bone marrow (BM) cells in GM-CSF and IL-6. Three subsets were identified based on their differential expression of CD14, CD33, CD34 and CD11b. Following flow sorting, assessment of the capacity of these subsets to suppress anti-CD3/CD28-stimulated CD4 and CD8 T cell proliferation revealed that the most potent population was CD14hiCD33â/loCD34loCD11bhi. These BM-derived mMDSC markedly increased the incidence of CD4+CD25+CD127âFoxp3+ regulatory T cells in responder T cell populations. They offer potential value in testing the therapeutic efficacy of immunoregulatory mMDSC for the promotion of tolerance in nonhuman primate transplant models.
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Authors
Alan F. Zahorchak, Angelica Perez-Gutierrez, Mohamed B. Ezzelarab, Angus W. Thomson,