共 129 条
Programming dendritic cells to induce TH2 and tolerogenic responses
被引:283
作者:

Pulendran, Bali
论文数: 0 引用数: 0
h-index: 0
机构:
Emory Vaccine Ctr, Atlanta, GA USA Emory Vaccine Ctr, Atlanta, GA USA

Tang, Hua
论文数: 0 引用数: 0
h-index: 0
机构:
Emory Vaccine Ctr, Atlanta, GA USA Emory Vaccine Ctr, Atlanta, GA USA

Manicassamy, Santhakumar
论文数: 0 引用数: 0
h-index: 0
机构:
Emory Vaccine Ctr, Atlanta, GA USA Emory Vaccine Ctr, Atlanta, GA USA
机构:
[1] Emory Vaccine Ctr, Atlanta, GA USA
基金:
美国国家卫生研究院;
关键词:
T-HELPER-CELL;
SIGNAL-REGULATED KINASE;
ACTIVATED PROTEIN-KINASE;
ANTIGEN-PRESENTING CELLS;
THYMIC STROMAL LYMPHOPOIETIN;
TRANSCRIPTION FACTOR FOXP3;
INNATE IMMUNE-SYSTEM;
IN-VIVO;
TH2;
RESPONSES;
AIRWAY INFLAMMATION;
D O I:
10.1038/ni.1894
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
A fundamental puzzle in immunology is how the immune system decides what types of immune responses to launch against different stimuli. Although much is known about control of T helper type 1 (T(H)1) and T(H)17 responses, the mechanisms that initiate T(H)2 and T regulatory (T-reg) responses remain obscure. Emerging studies suggest a fundamental role for the innate immune system, particularly dendritic cells (DCs), in this process. We review these studies, and suggest that the innate control of T(H)2 and T-reg responses can be viewed as different hierarchies of organization, in which DCs, their innate receptors and signaling networks, and their interactions with other cells and local microenvironments represent different levels of the hierarchy.
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收藏
页码:647 / 655
页数:9
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