Human fetal lymphoid tissue-inducer cells are interleukin 17-producing precursors to RORC+ CD127+ natural killer-like cells

被引:545
作者
Cupedo, Tom [1 ,2 ]
Crellin, Natasha K. [3 ]
Papazian, Natalie [1 ]
Rombouts, Elwin J. [1 ]
Weijer, Kees [2 ]
Grogan, Jane L. [3 ]
Fibbe, Willem E. [4 ]
Cornelissen, Jan J. [1 ]
Spits, Hergen [2 ,3 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Hematol, NL-3000 CA Rotterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, NL-1105 AZ Amsterdam, Netherlands
[3] Genentech Inc, Dept Immunol, San Francisco, CA 94080 USA
[4] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Transfus, NL-2300 RC Leiden, Netherlands
关键词
COLONY-STIMULATING FACTOR; T-CELL; B-CELL; AUTOIMMUNE-DISEASE; ORGAN DEVELOPMENT; GENE-EXPRESSION; PEYERS-PATCHES; NK-CELLS; GAMMA-T; SPI-B;
D O I
10.1038/ni.1668
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The human body contains over 500 individual lymph nodes, yet the biology of their formation is poorly understood. Here we identify human lymphoid tissue-inducer cells (LTi cells) as lineage-negative RORC+ CD127(+) cells with the functional ability to interact with mesenchymal cells through lymphotoxin and tumor necrosis factor. Human LTi cells were committed natural killer (NK) cell precursors that produced interleukin 17 (IL-17) and IL-22. In vitro, LTi cells gave rise to RORC+ CD127+ NK cells that retained the ability to produce IL-17 and IL-22. Postnatally, similar populations of LTi cell-like cells and RORC+ CD127+ NK cells were present in tonsils, and both secreted IL-17 and IL-22 but no interferon-gamma. Our data indicate that lymph node organogenesis is controlled by an NK cell precursor population with adaptive immune features and demonstrate a previously unappreciated link between the innate and adaptive immune systems.
引用
收藏
页码:66 / 74
页数:9
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