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10.3389/fmed.2017.00092

http://scihub22266oqcxt.onion/10.3389/fmed.2017.00092
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C5484767!5484767!28702457
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suck abstract from ncbi


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pmid28702457      Front+Med+(Lausanne) 2017 ; 4 (ä): ä
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  • Multiple Myeloma Cells Express Key Immunoregulatory Cytokines and Modulate the Monocyte Migratory Response #MMPMID28702457
  • Freire-de-Lima L; Nardy AFFR; Ramos-Junior ES; Conde L; Santos Lemos J; da Fonseca LM; Lima JE; Maiolino A; Morrot A
  • Front Med (Lausanne) 2017[]; 4 (ä): ä PMID28702457show ga
  • Multiple myeloma (MM) is a plasma cell disorder that still remains incurable. The immune dysfunction of the host is a striking characteristic of MM, leading to tumor growth and reducing the survival rate of patients. Monocytes are precursors of conventional dendritic cells (DCs), a major player in the immunity mechanisms driving protective T cell responses against tumor. Herein, we report that human MM RPMI 8226 cell line shows a pronounced chemoattractant activity for monocytes and also expresses enhanced levels of the leukocyte chemotactic cytokines CXCL12, CCL5, MIP-1?, and CXCL10 in association with elevated levels of both key immunoregulatory interleukins such as IL-4 and IL-10. This cytokine profile was observed together with reduced expression of IFN-? by MM RPMI 8226 cell line, a determinant interleukin involved in the acquisition of cellular-mediated protective responses against tumor cells. We further demonstrate that MM RPMI 8226 cell line expresses elevated levels of soluble form of the intercellular adhesion molecule-1 known to inhibit antitumoral T cell responses. This attractive modulation of immune responses by MM cells might provide a means to impair early antitumor responses during the establishment of cytokine-mediated immunosuppressive tumor niche.
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