What is immune privilege (not)?

被引:540
作者
Galea, Ian [1 ]
Bechmann, Ingo
Perry, V. Hugh
机构
[1] Univ Southampton, Sch Biol Sci, CNS Inflammat Grp, Southampton SO16 7PX, Hants, England
[2] Univ Frankfurt, Inst Clin Neuroanat, D-60590 Frankfurt, Germany
关键词
CENTRAL-NERVOUS-SYSTEM; BACILLUS-CALMETTE-GUERIN; BLOOD-BRAIN-BARRIER; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; SPLEEN MACROPHAGES DIFFERENTIATE; ANTIGEN-PRESENTING CELLS; DRAINING LYMPH-NODES; MICROGLIA-LIKE CELLS; REGULATORY T-CELLS; MULTIPLE-SCLEROSIS;
D O I
10.1016/j.it.2006.11.004
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 'immune privilege' of the central nervous system (CNS) is indispensable for damage limitation during inflammation in a sensitive organ with poor regenerative capacity. It is a longstanding notion which, over time, has acquired several misconceptions and a lack of precision in its definition. In this article, we address these issues and re-define CNS immune privilege in the light of recent data. We show how it is far from absolute, and how it varies with age and brain region. Immune privilege in the CNS is often mis-attributed wholly to the blood-brain barrier. We discuss the pivotal role of the specialization of the afferent arm of adaptive immunity in the brain, which results in a lack of cell-mediated antigen drainage to the cervical lymph nodes although soluble drainage to these nodes is well described. It is now increasingly recognized how immune privilege is maintained actively as a result of the immunoregulatory characteristics of the CNS-resident cells and their microenvironment.
引用
收藏
页码:12 / 18
页数:7
相关论文
共 87 条
[1]  
Adams S, 1998, J IMMUNOL, V161, P1853
[2]   BRAIN MICROGLIA CONSTITUTIVELY EXPRESS BETA-2 INTEGRINS [J].
AKIYAMA, H ;
MCGEER, PL .
JOURNAL OF NEUROIMMUNOLOGY, 1990, 30 (01) :81-93
[3]  
Aloisi F, 1997, J IMMUNOL, V159, P1604
[4]   THE ACUTE INFLAMMATORY RESPONSE TO LIPOPOLYSACCHARIDE IN CNS PARENCHYMA DIFFERS FROM THAT IN OTHER BODY-TISSUES [J].
ANDERSSON, PB ;
PERRY, VH ;
GORDON, S .
NEUROSCIENCE, 1992, 48 (01) :169-186
[5]   Age-related effects of interleukin-1 beta on polymorphonuclear neutrophil-dependent increases in blood-brain barrier permeability in rats [J].
Anthony, DC ;
Bolton, SJ ;
Fearn, S ;
Perry, VH .
BRAIN, 1997, 120 :435-444
[6]   T-cell apoptosis in inflammatory brain lesions - Destruction of T cells does not depend on antigen recognition [J].
Bauer, J ;
Bradl, M ;
Hickey, WF ;
Forss-Petter, S ;
Breitschopf, H ;
Linington, C ;
Wekerle, H ;
Lassmann, H .
AMERICAN JOURNAL OF PATHOLOGY, 1998, 153 (03) :715-724
[7]  
Bechmann I, 1999, GLIA, V27, P62, DOI 10.1002/(SICI)1098-1136(199907)27:1<62::AID-GLIA7>3.0.CO
[8]  
2-S
[9]   Role of the peroxisome proliferator-activated receptor-γ (PPAR-γ) and its natural ligand 15-deoxy-Δ12,14-prostaglandin J2 in the regulation of microglial functions [J].
Bernardo, A ;
Levi, G ;
Minghetti, L .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (07) :2215-2223
[10]   STUDIES ON THE PROBLEM OF CORNEAL HOMOGRAFTS [J].
BILLINGHAM, RE ;
BOSWELL, T .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1953, 141 (904) :392-+