The why and how of thymocyte negative selection

被引:54
作者
Siggs, OM
Makaroff, LE
Liston, A [1 ]
机构
[1] Australian Natl Univ, John Curtin Sch Med Res, Canberra, ACT 2601, Australia
[2] Australian Natl Univ, Sch Biochem & Mol Biol, Canberra, ACT 2601, Australia
基金
英国惠康基金; 美国国家卫生研究院; 英国医学研究理事会;
关键词
D O I
10.1016/j.coi.2006.01.001
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 generation of T cell receptor (TCR) sequence diversity is the strength of adaptive immunity, yet is also the Achilles' heel. To purge highly self-reactive T cells from the immune system, generation of diversity has coevolved with a mechanism of negative selection. Recent studies have revealed new insights addressing the why and how of negative selection by examining situations in which negative selection has failed in human and animals models of autoimmunity. Both thymocyte extrinsic and intrinsic mechanisms are required to restrict the TCR repertoire to a non-autoreactive set. Negative selection also ensures that T cells emerge with receptors that are focussed on the peptide moiety of MHC-peptide complexes.
引用
收藏
页码:175 / 183
页数:9
相关论文
共 52 条
[1]   High-resolution physical and transcriptional mapping of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy locus on chromosome 21q22.3 FISH [J].
Aaltonen, J ;
HorelliKuitunen, N ;
Fan, JB ;
Bjorses, P ;
Perheentupa, J ;
Myers, R ;
Palotie, A ;
Peltonen, L .
GENOME RESEARCH, 1997, 7 (08) :820-829
[2]   Promiscuous thymic expression of an autoantigen gene does not result in negative selection of pathogenic T cells [J].
Allen, S ;
Read, S ;
DiPaolo, R ;
McHugh, RS ;
Shevach, EM ;
Gleeson, PA ;
van Driel, IR .
JOURNAL OF IMMUNOLOGY, 2005, 175 (09) :5759-5764
[3]   The cellular mechanism of Aire control of T cell tolerance [J].
Anderson, MS ;
Venanzi, ES ;
Chen, ZB ;
Berzins, SP ;
Benoist, C ;
Mathis, D .
IMMUNITY, 2005, 23 (02) :227-239
[4]   Projection of an immunological self shadow within the thymus by the aire protein [J].
Anderson, MS ;
Venanzi, ES ;
Klein, L ;
Chen, ZB ;
Berzins, SP ;
Turley, SJ ;
von Boehmer, H ;
Bronson, R ;
Dierich, A ;
Benoist, C ;
Mathis, D .
SCIENCE, 2002, 298 (5597) :1395-1401
[5]   β-subunit assembly is essential for the correct packing and the stable membrane insertion of the H,K-ATPase α-subunit [J].
Beggah, AT ;
Béguin, P ;
Bamberg, K ;
Sachs, G ;
Geering, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (12) :8217-8223
[6]   Diabetes protection and restoration of thymocyte apoptosis in NOD Idd6 congenic strains [J].
Bergman, ML ;
Duarte, N ;
Campino, S ;
Lundholm, M ;
Motta, V ;
Lejon, K ;
Penha-Gonçalves, C ;
Holmberg, D .
DIABETES, 2003, 52 (07) :1677-1682
[7]   BH3-only Bcl-2 family member Bim is required for apoptosis of autoreactive thymocytes [J].
Bouillet, P ;
Purton, JF ;
Godfrey, DI ;
Zhang, LC ;
Coultas, L ;
Puthalakath, H ;
Pellegrini, M ;
Cory, S ;
Adams, JM ;
Strasser, A .
NATURE, 2002, 415 (6874) :922-926
[8]  
BURNET M, 1959, BMJ-BRIT MED J, V5154, P720
[9]   BCL-2, BCL-XL sequester BH3 domain-only molecules preventing BAX- and BAK-mediated mitochondrial apoptosis [J].
Cheng, EHYA ;
Wei, MC ;
Weiler, S ;
Flavell, RA ;
Mak, TW ;
Lindsten, T ;
Korsmeyer, SJ .
MOLECULAR CELL, 2001, 8 (03) :705-711
[10]   Enhanced pathogenicity of diabetogenic T cells escaping a non-MHC gene-controlled near death experience [J].
Choisy-Rossi, CM ;
Holl, TM ;
Pierce, MA ;
Chapman, HD ;
Serreze, DV .
JOURNAL OF IMMUNOLOGY, 2004, 173 (06) :3791-3800