T Follicular Helper, but Not Th1, Cell Differentiation in the Absence of Conventional Dendritic Cells

被引:20
|
作者
Dahlgren, Madelene W. [1 ]
Gustafsson-Hedberg, Tobias [2 ]
Livingston, Megan [2 ]
Cucak, Helena [1 ]
Alsen, Samuel [1 ,2 ]
Yrlid, Ulf [2 ]
Johansson-Lindbom, Bengt [1 ]
机构
[1] Lund Univ, Immunol Sect, S-22184 Lund, Sweden
[2] Univ Gothenburg, Dept Microbiol & Immunol, Mucosal Immunobiol & Vaccine Ctr, Inst Biomed, S-40530 Gothenburg, Sweden
来源
JOURNAL OF IMMUNOLOGY | 2015年 / 194卷 / 11期
基金
瑞典研究理事会;
关键词
TRANSCRIPTION-FACTOR; IN-VIVO; B-CELLS; CHEMOKINE RECEPTOR; MEDIATED-IMMUNITY; BCL-6; EXPRESSION; LYMPH-NODES; RESPONSES; ANTIGEN; INFECTION;
D O I
10.4049/jimmunol.1401938
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Development of long-lived humoral immunity is dependent on CXCR5-expressing T follicular helper (Tfh) cells, which develop concomitantly to effector Th cells that support cellular immunity. Conventional dendritic cells (cDCs) are critical APCs for initial priming of naive CD4(+) T cells but, importantly, also provide accessory signals that govern effector Th cell commitment. To define the accessory role of cDCs during the concurrent development of Tfh and effector Th1 cells, we performed high-dose Ag immunization in conjunction with the Th1-biased adjuvant polyinosinic: polycytidylic acid (pI:C). In the absence of cDCs, pI: C failed to induce Th1 cell commitment and IgG2c production. However, cDC depletion did not impair Tfh cell differentiation or germinal center formation, and long-lived IgG1 responses of unaltered affinity developed in mice lacking cDCs at the time point for immunization. Thus, cDCs are required for the pI: C-driven Th1 cell fate commitment but have no crucial accessory function in relation to Tfh cell differentiation.
引用
收藏
页码:5187 / 5199
页数:13
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