A Single Subset of Dendritic Cells Controls the Cytokine Bias of Natural Killer T Cell Responses to Diverse Glycolipid Antigens

被引:87
作者
Arora, Pooja [1 ]
Baena, Andres [3 ]
Yu, Karl O. A. [4 ]
Saini, Neeraj K. [1 ]
Kharkwal, Shalu S. [1 ]
Goldberg, Michael F. [1 ]
Kunnath-Velayudhan, Shajo [1 ]
Carreno, Leandro J. [1 ,5 ]
Venkataswamy, Manjunatha M. [6 ]
Kim, John [1 ]
Lazar-Molnar, Eszter [1 ]
Lauvau, Gregoire [1 ]
Chang, Young-tae [7 ,8 ,9 ]
Liu, Zheng [10 ]
Bittman, Robert [10 ]
Al-Shamkhani, Aymen [11 ]
Cox, Liam R. [12 ]
Jervis, Peter J. [13 ]
Veerapen, Natacha [13 ]
Besra, Gurdyal S. [13 ]
Porcelli, Steven A. [1 ,2 ]
机构
[1] Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[3] Univ Antioquia UdeA, Fac Med, Grp Inmunol Celular & Inmunogenet GICIG, Dept Microbiol & Parasitol, Medellin 05001000, Colombia
[4] Univ Chicago, Comer Childrens Hosp, Chicago, IL 60637 USA
[5] Univ Chile, Fac Med, Millennium Inst Immunol & Immunotherapy, Santiago 8380453, Chile
[6] Natl Inst Mental Hlth & Neurosci, Bangalore 560029, Karnataka, India
[7] Natl Univ Singapore, Dept Chem, Biopolis 117543, Singapore
[8] Natl Univ Singapore, Med Chem Programme, Biopolis 117543, Singapore
[9] ASTAR, Singapore Bioimaging Consortium, Biopolis 117543, Singapore
[10] CUNY Queens Coll, Dept Chem & Biochem, Flushing, NY 11367 USA
[11] Univ Southampton, Canc Sci Acad Unit, Fac Med, Southampton SO16 6YD, Hants, England
[12] Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
[13] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
基金
英国惠康基金;
关键词
NKT CELLS; ACTIVATION; FLUORESCENCE; MECHANISM; VARIANTS; PATHWAYS;
D O I
10.1016/j.immuni.2013.12.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Many hematopoietic cell types express CD1d and are capable of presenting glycolipid antigens to invariant natural killer T cells (iNKT cells). However, the question of which cells are the principal presenters of glycolipid antigens in vivo remains controversial, and it has been suggested that this might vary depending on the structure of a particular glycolipid antigen. Here we have shown that a single type of cell, the CD8 alpha(+) DEC-205(+) dendritic cell, was mainly responsible for capturing and presenting a variety of different glycolipid antigens, including multiple forms of alpha-galactosylceramide that stimulate widely divergent cytokine responses. After glycolipid presentation, these dendritic cells rapidly altered their expression of various costimulatory and coinhibitory molecules in a manner that was dependent on the structure of the antigen. These findings show flexibility in the outcome of two-way communication between CD8 alpha(+) dendritic cells and iNKT cells, providing a mechanism for biasing toward either proinflammatory or anti-inflammatory responses.
引用
收藏
页码:105 / 116
页数:12
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