| Literature DB >> 29900053 |
Baptiste Lamarthée1,2, Frédéric de Vassoigne1,2, Florent Malard1,2, Nicolas Stocker1, Inès Boussen1, Clémence Médiavilla1, Ruoping Tang2, Fanny Fava2, Laurent Garderet2, Zora Marjanovic2, Eolia Brissot1,2, Mohamad Mohty1,2, Béatrice Gaugler1,2.
Abstract
Multiple myeloma (MM) results from expansion of abnormal plasma cells in the bone marrow (BM). Previous studies have shown that monocytes play a crucial role in MM pathophysiology. A 6-sulfo LacNAc-expressing population of dendritic cells (Slan-DCs) that overlaps with intermediate and non-classical monocytes in terms of phenotype has been described. Slan-DCs represent a circulating and tissue proinflammatory myeloid population which has been shown to play a role in different cancer contexts, and which exhibits a remarkable plasticity. Herein, we studied Slan-DCs from the BM and blood of MM patients. We performed quantitative and functional analyses of these cells from 54 patients with newly diagnosed, symptomatic MM, 21 patients with MGUS and 24 responding MM patients. We found that circulating Slan-DCs were significantly decreased in MM patients as compared to those of healthy donors or patients with MGUS, while CD14+CD16+ intermediate monocytes accumulate in the BM. Moreover, after activation with TLR7/8 ligand R848, IL-12-producing Slan-DCs from the BM or peripheral blood from MM patients were decreased as compared with healthy donors. We show that MM cell lines or MM cells isolated from patients at diagnosis were able to inhibit the production of IL-12 by Slan-DCs, as well as to shift the phenotype of Slan-DCs towards an intermediate monocyte-like phenotype. Finally, Slan-DCs that have been cultured with MM cells reduced their capacity to induce T cell proliferation and Th1 polarization. We conclude that Slan-DCs represent previously unrecognized players in MM development and may represent a therapeutic target.Entities:
Keywords: Immunosurveillance; Slan-DC; antitumor T cell; dendritic cells; immunotherapy; multiple myeloma
Year: 2018 PMID: 29900053 PMCID: PMC5993501 DOI: 10.1080/2162402X.2018.1444411
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110