Effective collaboration between marginal metallophilic macrophages and CD8+ dendritic cells in the generation of cytotoxic T cells

被引:143
作者
Backer, Ronald [1 ]
Schwandt, Timo [2 ]
Greuter, Mascha [1 ]
Oosting, Marije [1 ]
Jungerkes, Frank [2 ]
Tuting, Thomas [2 ]
Boon, Louis [3 ]
O'Toole, Tom [1 ]
Kraal, Georg [1 ]
Limmer, Andreas [2 ]
den Haan, Joke M. M. [1 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Mol Cell Biol & Immunol, NL-1007 MB Amsterdam, Netherlands
[2] Univ Bonn, Inst Mol Med & Expt Immunol, D-53105 Bonn, Germany
[3] Bioceros BV, NL-3584 CM Utrecht, Netherlands
关键词
antigen presentation; infection; ANTIGENS IN-VIVO; ZONE MACROPHAGES; MONOCLONAL-ANTIBODY; CROSS-PRESENTATION; MOUSE SPLEEN; IMMUNITY; VIRUS; VACCINATION; INFECTION; DEPLETION;
D O I
10.1073/pnas.0909541107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The spleen is the lymphoid organ that induces immune responses toward blood-borne pathogens. Specialized macrophages in the splenic marginal zone are strategically positioned to phagocytose pathogens and cell debris, but are not known to play a role in the activation of T-cell responses. Here we demonstrate that splenic marginal metallophilic macrophages (MMM) are essential for cross-presentation of blood-borne antigens by splenic dendritic cells (DCs). Our data demonstrate that antigens targeted to MMM as well as blood-borne adenoviruses are efficiently captured by MMM and exclusively transferred to splenic CD8(+) DCs for cross-presentation and for the activation of cytotoxic T lymphocytes. Depletion of macrophages in the marginal zone prevents cytotoxic T-lymphocyte activation by CD8(+) DCs after antibody targeting or adenovirus infection. Moreover, we show that tumor antigen targeting to MMM is very effective as antitumor immunotherapy. Our studies point to an important role for splenic MMM in the initial steps of CD8(+) T-cell immunity by capturing and concentrating blood-borne antigens and the transfer to cross-presenting DCs which can be used to design vaccination strategies to induce antitumor cytotoxic T-cell immunity.
引用
收藏
页码:216 / 221
页数:6
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