共 168 条
Regulatory T cells in autoimmune neuroinflammation
被引:229
作者:
Kleinewietfeld, Markus
[1
,2
,3
,4
]
Hafler, David A.
[1
,2
,3
]
机构:
[1] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[3] Broad Inst MIT & Harvard, Cambridge, MA USA
[4] Dresden Univ Technol TUD, Fac Med, Dresden, Germany
基金:
美国国家卫生研究院;
关键词:
autoimmunity;
Treg;
multiple sclerosis;
FoxP3;
regulatory T cells;
Tr1;
MULTIPLE-SCLEROSIS PATIENTS;
HUMAN DENDRITIC CELLS;
FOXP3;
EXPRESSION;
TREG CELLS;
TH17;
CELLS;
IN-VITRO;
TRANSCRIPTION FACTOR;
VITAMIN-D;
EX-VIVO;
INDOLEAMINE 2,3-DIOXYGENASE;
D O I:
10.1111/imr.12169
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:
Regulatory T cells are the central element for the maintenance of peripheral tolerance. Several subtypes of regulatory T (Treg) cells have been described, and most of them belong to the CD4(+) T-helper (Th) cell lineage. These specific subtypes can be discriminated according to phenotype and function. Forkhead box protein 3 (FoxP3)-expressing natural Treg cells (Tregs) and IL-10-producing, T-regulatory type 1 cells (Tr1) are the best-studied types of CD4(+) regulatory T cells in humans and experimental animal models. It was shown that they play a crucial role during autoimmune neuroinflammation. Both cells types seem to be particularly important for multiple sclerosis (MS). Here, we discuss the role of CD4(+) regulatory T cells in autoimmune neuroinflammation with an emphasis on Tregs and Tr1 cells in MS.
引用
收藏
页码:231 / 244
页数:14
相关论文

