Foxp3 expression in T regulatory cells and other cell lineages

被引:95
作者
Devaud, Christel [1 ,2 ]
Darcy, Phillip K. [1 ,3 ]
Kershaw, Michael H. [1 ,2 ,3 ]
机构
[1] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Canc Immunol Res Program, Parkville, Vic 3010, Australia
[2] Peter MacCallum Canc Ctr, Canc Immunol Res Program, Melbourne, Vic 3002, Australia
[3] Monash Univ, Dept Immunol, Prahran, Vic 3181, Australia
基金
英国医学研究理事会;
关键词
Foxp3; T cells; Tumor; Epithelial cells; Macrophages; TRANSCRIPTION FACTOR FOXP3; INVARIANT NKT CELLS; SCURFY SF MOUSE; BREAST-CANCER; TUMOR-CELLS; TGF-BETA; HISTONE ACETYLTRANSFERASE; ANTITUMOR IMMUNITY; EPITHELIAL-CELLS; EFFECTOR-CELLS;
D O I
10.1007/s00262-014-1581-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Forkhead box P3 (Foxp3) is an important transcription factor that belongs to the forkhead/winged-helix family of transcriptional regulators. Foxp3 has been extensively studied over the past 13 years as a master regulator of transcription in a specific T-cell type, CD4(+) regulatory T cells (Treg), both in humans and in mice. Compelling data characterize Foxp3 as critically important and necessary for the development and the differentiation of Treg. It has been considered initially as the only specific marker for Treg. However, recent work has proposed that Foxp3 can be expressed by other types of lymphoid cells or myeloid cells and also by some non-hematopoietic cells such as epithelial cells. It remains controversial about the expression of Foxp3 in cells other than Treg, but understanding the potential expression and function of this master regulator in different cell subsets could have a wide range of implications for immune tolerance and several pathologies including autoimmune disorders and immune responses to cancer.
引用
收藏
页码:869 / 876
页数:8
相关论文
共 82 条
[1]
Activation-induced FOXP3 in human T effector cells does not suppress proliferation or cytokine production [J].
Allan, Sarah E. ;
Crome, Sarah Q. ;
Crellin, Natasha K. ;
Passerini, Laura ;
Steiner, Theodore S. ;
Bacchetta, Rosa ;
Roncarolo, Maria G. ;
Levings, Megan K. .
INTERNATIONAL IMMUNOLOGY, 2007, 19 (04) :345-354
[2]
The role of 2 FOXP3 isoforms in the generation of human CD4+ Tregs [J].
Allan, SE ;
Passerini, L ;
Bacchetta, R ;
Crellin, N ;
Dai, MY ;
Orban, PC ;
Ziegler, SF ;
Roncarolo, MG ;
Levings, MK .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (11) :3276-3284
[3]
Foxp3-positive macrophages display immunosuppressive properties and promote tumor growth (vol 208, pg 1485, 2011) [J].
Manrique, Soraya Zorro ;
Correa, Maria Adelaida Duque ;
Hoelzinger, Dominique B. ;
Dominguez, Ana Lucia ;
Mirza, Noweeda ;
Lin, Hsi-Hsien ;
Stein-Streilein, Joan ;
Gordon, Siamon ;
Lustgarten, Joseph .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (12) :2561-2561
[4]
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 [J].
Bennett, CL ;
Christie, J ;
Ramsdell, F ;
Brunkow, ME ;
Ferguson, PJ ;
Whitesell, L ;
Kelly, TE ;
Saulsbury, FT ;
Chance, PF ;
Ochs, HD .
NATURE GENETICS, 2001, 27 (01) :20-21
[5]
Induced CD4+Foxp3+ Regulatory T Cells in Immune Tolerance [J].
Bilate, Angelina M. ;
Lafaille, Juan J. .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 30, 2012, 30 :733-758
[6]
Parallel expansion of human virus-specific FoxP3- effector memory and de novo-generated FoxP3+ regulatory CD8+ T cells upon antigen recognition in vitro [J].
Billerbeck, Eva ;
Blum, Hubert E. ;
Thimme, Robert .
JOURNAL OF IMMUNOLOGY, 2007, 179 (02) :1039-1048
[7]
TCR stimulation with modified anti-CD3 mAb expands CD8+ T cell population and induces CD8+CD25+ Tregs [J].
Bisikirska, B ;
Colgan, J ;
Luban, J ;
Bluestone, JA ;
Herold, KC .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (10) :2904-2913
[8]
BLAIR PJ, 1994, J IMMUNOL, V153, P3764
[9]
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse [J].
Brunkow, ME ;
Jeffery, EW ;
Hjerrild, KA ;
Paeper, B ;
Clark, LB ;
Yasayko, SA ;
Wilkinson, JE ;
Galas, D ;
Ziegler, SF ;
Ramsdell, F .
NATURE GENETICS, 2001, 27 (01) :68-73
[10]
Phenotypical and functional specialization of FOXP3+ regulatory T cells [J].
Campbell, Daniel J. ;
Koch, Meghan A. .
NATURE REVIEWS IMMUNOLOGY, 2011, 11 (02) :119-130