Monocytic myeloid-derived suppressor cells generated from rhesus macaque bone marrow enrich for regulatory T cells.

Monocytic myeloid-derived suppressor cells generated from rhesus macaque bone marrow enrich for regulatory T cells.
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DOI:
10.1016/j.cellimm.2018.04.013
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发表时间:
2018-07
影响因子:
4.3
通讯作者:
Thomson AW
Thomson AW
中科院分区:
医学4区
文献类型:
--
作者:
Zahorchak AF;Perez-Gutierrez A;Ezzelarab MB;Thomson AW

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从正常恒河猴骨髓(BM)细胞经GM-−和IL-6培养7天后,获得了可能的单核细胞来源的髓系抑制细胞(MMDSC;Lineage HLADR−/lo)。根据CD14、CD33、CD34和CD11b的表达差异,确定了三个亚群。Flow分选后,对这些亚群抑制抗CD3/CD28刺激的CD_4和CD_8T细胞增殖的能力的评估表明,最有效的群体是CD14hiCD33−/loCD34loCD11bhi。这些骨髓来源的mMDSC显著增加应答T细胞群中−+CD25+CD127Foxp3+调节性T细胞的发生率。它们在检测免疫调节性mMDSC促进非人类灵长类移植耐受的疗效方面提供了潜在的价值。
Putative monocytic myeloid-derived suppressor cells (mMDSC; lineage−HLA-DR−/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 CD14hiCD33−/loCD34loCD11bhi. These BM-derived mMDSC markedly increased the incidence of CD4+CD25+CD127−Foxp3+ 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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