Defining the Signature of VISTA on Myeloid Cell Chemokine Responsiveness

被引:42
作者
Broughton, Thomas W. K. [1 ,2 ]
ElTanbouly, Mohamed A. [1 ]
Schaafsma, Evelien [1 ]
Deng, Jie [1 ]
Sarde, Aurelien [1 ]
Croteau, Walburga [1 ]
Li, Jiannan [1 ]
Nowak, Elizabeth C. [1 ]
Mabaera, Rodwell [1 ,3 ]
Smits, Nicole C. [1 ]
Kuta, Anna [4 ]
Noelle, Randolph J. [1 ]
Lines, J. Louise [1 ]
机构
[1] Geisel Sch Med Dartmouth, Dept Microbiol & Immunol, Norris Cotton Canc Ctr, Lebanon, NH 03755 USA
[2] Kings Coll London, Div Transplantat Immunol & Mucosal Biol, Fac Life Sci & Med, London, England
[3] Dartmouth Hitchcock Med Ctr, Sect Hematol & Oncol, Lebanon, NH 03766 USA
[4] Immunext Corp, Lebanon, NH USA
关键词
VISTA; macrophage; immune checkpoint; chemokine; migration; CHEMOATTRACTANT PROTEIN-1 MCP-1; IN-VITRO; TRANSCRIPTIONAL CONTROL; IMMUNE-RESPONSE; T-CELLS; MONOCYTES; MACROPHAGES; EXPRESSION; DIFFERENTIATION; NEUTROPHILS;
D O I
10.3389/fimmu.2019.02641
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The role of negative checkpoint regulators (NCRs) in human health and disease cannot be overstated. V-domain Ig-containing Suppressor of T-cell Activation (VISTA) is an Ig superfamily protein predominantly expressed within the hematopoietic compartment and has been studied for its role in the negative regulation of T cell responses. The findings presented in this study show that, unlike all other NCRs, VISTA deficiency dramatically impacts on macrophage cytokine and chemokine production, as well as the chemotactic response of VISTA-deficient macrophages. A select group of inflammatory chemokines, including CCL2, CCL3, CCL4, and CCL5, was strikingly elevated in culture supernatants from VISTA KO macrophages. VISTA deficiency also altered chemokine receptor recycling and profoundly disrupted myeloid chemotaxis. The impact of VISTA deficiency on chemotaxis in vivo was apparent with the reduced ability of both KO macrophages and MDSCs to migrate to the tumor microenvironment. This is the first demonstration of an NCR impacting on myeloid mediator production and chemotaxis, and will guide the use of anti-VISTA therapeutics to manipulate the chemotaxis of inflammatory macrophages or immunosuppressive MDSCs in inflammatory diseases and cancer.
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页数:13
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