Regulatory T cells in CNS injury: the simple, the complex and the confused

被引:46
作者
Walsh, James T.
Kipnis, Jonathan [1 ]
机构
[1] Univ Virginia, Dept Neurosci, Grad Program Neurosci, Charlottesville, VA 22908 USA
关键词
CENTRAL-NERVOUS-SYSTEM; SPINAL-CORD-INJURY; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; ANTI-CD25; MONOCLONAL-ANTIBODY; MYELIN BASIC-PROTEIN; OPTIC-NERVE; MULTIPLE-SCLEROSIS; UP-REGULATION; CUTTING EDGE; BRAIN TRAUMA;
D O I
10.1016/j.molmed.2011.05.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulatory CD4(+)CD25(+)Foxp3(+) T cells (Tregs) have been the focus of significant attention for their role in controlling immune responses. Although knowledge of Treg biology has burgeoned, wide gaps remain in our understanding of Treg function under both normal and pathological conditions. Pioneering studies demonstrated roles for Tregs in cancer and autoimmune diseases, including experimental autoimmune encephalitis, and this knowledge is often applied to other pathologies including neurodegenerative conditions. However, differences between immunity in neurodegeneration and in malignancy or autoimmunity are often neglected. Thus, Treg manipulations in central nervous system (CNS) neurodegenerative conditions often yield unexpected outcomes. In this piece, we explore how the immunology of neurodegeneration differs from that of cancer and autoimmunity and how these differences create confusion about the role of Tregs in neurodegenerative conditions.
引用
收藏
页码:541 / 547
页数:7
相关论文
共 72 条
[1]   Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[2]   Caspase inhibition therapy abolishes brain trauma-induced increases in Aβ peptide:: Implications for clinical outcome [J].
Abrahamson, EE ;
Ikonomovic, MD ;
Ciallella, JR ;
Hope, CE ;
Paljug, WR ;
Isanski, BA ;
Flood, DG ;
Clark, RSB ;
DeKosky, ST .
EXPERIMENTAL NEUROLOGY, 2006, 197 (02) :437-450
[3]   CAUDAL SPINAL-CORD OF THE TELEOST STERNARCHUS-ALBIFRONS RESEMBLES REGENERATING CORD [J].
ANDERSON, MJ ;
WAXMAN, SG .
ANATOMICAL RECORD, 1983, 205 (01) :85-92
[4]  
BARKER CF, 1977, ADV IMMUNOL, V25, P1
[5]   CD4+T cells support glial neuroprotection, slow disease progression, and modify glial morphology in an animal model of inherited ALS [J].
Beers, David R. ;
Henkel, Jenny S. ;
Zhao, Weihua ;
Wang, Jinghong ;
Appel, Stanley H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (40) :15558-15563
[6]   IMMUNOGENICITY AND TOLEROGENICITY OF SELF-MAJOR HISTOCOMPATIBILITY COMPLEX PEPTIDES [J].
BENICHOU, G ;
TAKIZAWA, PA ;
HO, PT ;
KILLION, CC ;
OLSON, CA ;
MCMILLAN, M ;
SERCARZ, EE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) :1341-1346
[7]   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
[8]   Opinion - Spinal cord repair strategies: why do they work? [J].
Bradbury, Elizabeth J. ;
McMahon, Stephen B. .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (08) :644-653
[9]   Pathophysiology of cerebral ischemia and brain trauma: Similarities and differences [J].
Bramlett, HM ;
Dietrich, WD .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2004, 24 (02) :133-150
[10]   Regulatory T cells maintain long-term tolerance to myelin basic protein by inducing a novel, dynamic state of T cell tolerance [J].
Cabbage, Sarah E. ;
Huseby, Eric S. ;
Sather, Blythe D. ;
Brabb, Thea ;
Liggitt, Denny ;
Goverman, Joan .
JOURNAL OF IMMUNOLOGY, 2007, 178 (02) :887-896