Activated Vγ9Vδ2 T Cells Trigger Granulocyte Functions via MCP-2 Release

被引:37
作者
Agrati, Chiara [1 ]
Cimini, Eleonora [1 ]
Sacchi, Alessandra [1 ]
Bordoni, Veronica [1 ]
Gioia, Cristiana [1 ]
Casetti, Rita [1 ]
Turchi, Federica [1 ]
Tripodi, Marco [1 ]
Martini, Federico [1 ]
机构
[1] Natl Inst Infect Dis Lazzaro Spallanzani, IRCCS, Rome, Italy
关键词
NONPEPTIDE ANTIGENS; MYCOBACTERIUM-TUBERCULOSIS; ANTIVIRAL IMMUNITY; ZOLEDRONIC ACID; CC CHEMOKINES; IN-VITRO; INFECTION; DEFENSINS; STIMULATION; LYMPHOCYTES;
D O I
10.4049/jimmunol.182.1.522
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
V gamma 9V delta 2 T cells display a broad antimicrobial activity by directly killing infected cells and by inducing an effective adaptive immune response. The activation of V gamma 9V delta 2 T cells by aminobisphosphonate drugs such as zoledronic acid (ZOL) results in a massive release of cytokines and chemokines that may induce a bystander activation of other immune cells. The aim of this work was to evaluate the ability of soluble factors released by ZOL-activated V gamma 9V delta 2 T cells to induce granulocyte activation. We showed that soluble factors released by ZOL-stimulated V gamma 9V delta 2 T cells activate granulocytes by inducing their chemotaxis, phagocytosis, and alpha-defensins release. Proteomic analysis allowed us to identify a number of cytokines and chemokines specifically released by activated V gamma 9V delta 2 T cells. Moreover, MCP-2 depletion by neutralizing Ab revealed a critical role of this chemokine in induction of granulocyte alpha-defensins release. Altogether, these data show a V gamma 9V delta 2-mediated activation of granulocytes through a bystander mechanism, and confirm the wide ability of V gamma 9V delta 2 T-lymphocytes in orchestrating the immune response. In conclusion, an immune modulating strategy targeting V gamma 9V delta 2 T cells may represent a key switch to induce an effective and well-coordinated immune response, and can be proposed as a way to strengthen the immune competence during infectious diseases. The Journal of Immunology, 2009, 182: 522-529.
引用
收藏
页码:522 / 529
页数:8
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