Dendritic cells in the CNS: immune regulators and therapeutic targets for multiple sclerosis treatment

被引:0
作者
Zozulya, Alla L. [2 ]
Reinke, Emily K. [2 ]
Ling, Changying [2 ]
Sandor, Matyas [2 ]
Fabry, Zsuzsanna [1 ]
机构
[1] Univ Wisconsin Madison, Sch Med & Publ Hlth, Dept Pathol & Lab Med, 1300 Univ Ave,6130 MSC, Madison, WI 53706 USA
[2] Univ Wisconsin Madison, Dept Pathol, Madison, WI 53706 USA
关键词
autoimmunity; blood-brain barrier; CNS; dendritic cell; experimental autoimmune encephalomyelitis; multiple sclerosis;
D O I
10.2217/14796708.2.1.97
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Dendritic cells (DCs) are essential antigen-presenting cells responsible for initiating cellular immune responses. The increasing interest in the mechanisms of DC trafficking has created new and exciting opportunities for bench-to-bedside therapies to treat autoimmune diseases of the central nervous system (CNS). However, tracking the migration of DCs in the CNS has proved to be more problematic owing to their low number in the immunologically privileged environment of the brain and high diversity as a cell population. A significant contributor to immune privilege in the brain is the blood-brain barrier, a unique structure recognized to regulate the entry of immune cells into the brain. Currently, it is hypothesized that the migration of DCs across the blood-brain barrier is critically important for the initiation of immune responses of CNS autoimmunity. This review summarizes the present knowledge on DC trafficking in the CNS and the main functions of these cells in initiating CNS autoimmunity. Selective identification of regulatory molecules and novel therapies to inhibit DC migration and function during CNS autoimmune diseases without affecting normal DC function under physiological conditions will be critical in treatments for neurological inflammatory diseases.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 66 条
[1]  
Adamson P, 1999, J IMMUNOL, V162, P2964
[2]  
Alt C, 2002, EUR J IMMUNOL, V32, P2133, DOI 10.1002/1521-4141(200208)32:8<2133::AID-IMMU2133>3.0.CO
[3]  
2-W
[4]   LNFPIII/LeX-stimulated macrophages activate natural killer cells via CD40-CD40L interaction [J].
Atochina, O ;
Harn, D .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2005, 12 (09) :1041-1049
[5]  
Baiu DC, 2006, J IMMUNOL IN PRESS
[6]   The clinical course of experimental autoimmune encephalomyelitis and inflammation is controlled by the expression of CD40 within the central nervous system [J].
Becher, B ;
Durell, BG ;
Miga, AV ;
Hickey, WF ;
Noelle, RJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (08) :967-974
[7]   Regulation of Th1 and Th2 lymphocyte migration by human adult brain endothelial cells [J].
Biernacki, K ;
Prat, A ;
Blain, M ;
Antel, JP .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2001, 60 (12) :1127-1136
[8]   The C-type lectin DC-SIGN (CD209) is an antigen-uptake receptor for Candida albicans on dendritic cells [J].
Cambi, A ;
Gijzen, K ;
de Vries, JM ;
Torensma, R ;
Joosten, B ;
Adema, GJ ;
Netea, MG ;
Kullberg, BJ ;
Romani, L ;
Figdor, CG .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (02) :532-538
[9]   Fms-like tyrosine kinase 3 ligand recruits plasmacytoid dendritic cells to the brain [J].
Curtin, James F. ;
King, Gwendalyn D. ;
Barcia, Carlos ;
Liu, Chunyan ;
Hubert, Franiqois X. ;
Guillonneau, Carole ;
Josien, Regis ;
Anegon, Ignacio ;
Lowenstein, Pedro R. ;
Castro, Maria G. .
JOURNAL OF IMMUNOLOGY, 2006, 176 (06) :3566-3577
[10]   Transfer of central nervous system autoantigens and presentation in secondary lymphoid organs [J].
de Vos, AF ;
van Meurs, M ;
Brok, HP ;
Boven, LA ;
Hintzen, RQ ;
van der Valk, P ;
Ravid, R ;
Rensing, S ;
Boon, L ;
't Hart, BA ;
Laman, JD .
JOURNAL OF IMMUNOLOGY, 2002, 169 (10) :5415-5423