Evaluating peptide repertoires within the context of thymocyte development

被引:10
作者
Barton, GM [1 ]
Rudensky, AY
机构
[1] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98195 USA
[2] Univ Washington, Mol & Cellular Biol Program, Seattle, WA 98195 USA
[3] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Howard Hughes Med Inst, Seattle, WA 98195 USA
关键词
MHC; peptides; selection; thymocyte;
D O I
10.1006/smim.1999.0199
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The process of antigen presentation by MHC molecules allows T cells to sample the proteins expressed within a particular cell. This sampling is in the form of short peptides bound within the grooves of MHC molecules displayed on the surface of cells. In the context of immune surveillance, this presentation allows the identification of infected cells by displaying peptides originating from foreign proteins within the cell. However, MHC-bound peptides play additional roles beyond serving as antigenic stimuli during an immune response. In fact, it has become clear that MHC-bound peptides derived from self proteins are critically involved in the development of T cells during selective events in the thymus. In this review we will discuss the nature of the population of MHC-bound peptides as it relates to thymocyte development, with particular emphasis on the recent finding that peptide- MHC complexes present at low levels can drive the positive selection of thymocytes.
引用
收藏
页码:417 / 422
页数:6
相关论文
共 37 条
[1]
PEPTIDE CONTRIBUTES TO THE SPECIFICITY OF POSITIVE SELECTION OF CD8+ T-CELLS IN THE THYMUS [J].
ASHTONRICKARDT, PG ;
VANKAER, L ;
SCHUMACHER, TNM ;
PLOEGH, HL ;
TONEGAWA, S .
CELL, 1993, 73 (05) :1041-1049
[2]
EVIDENCE FOR A DIFFERENTIAL AVIDITY MODEL OF T-CELL SELECTION IN THE THYMUS [J].
ASHTONRICKARDT, PG ;
BANDEIRA, A ;
DELANEY, JR ;
VANKAER, L ;
PIRCHER, HP ;
ZINKERNAGEL, RM ;
TONEGAWA, S .
CELL, 1994, 76 (04) :651-663
[3]
Requirement for diverse, low-abundance peptides in positive selection of T cells [J].
Barton, GM ;
Rudensky, AY .
SCIENCE, 1999, 283 (5398) :67-70
[4]
Positive selection of T cells: Fastidious or promiscuous? [J].
Benoist, C ;
Mathis, D .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (02) :245-249
[5]
Endosomal proteolysis and MHC class II function [J].
Chapman, HA .
CURRENT OPINION IN IMMUNOLOGY, 1998, 10 (01) :93-102
[6]
PREDOMINANT NATURALLY PROCESSED PEPTIDES BOUND TO HLA-DR1 ARE DERIVED FROM MHC-RELATED MOLECULES AND ARE HETEROGENEOUS IN SIZE [J].
CHICZ, RM ;
URBAN, RG ;
LANE, WS ;
GORGA, JC ;
STERN, LJ ;
VIGNALI, DAA ;
STROMINGER, JL .
NATURE, 1992, 358 (6389) :764-768
[7]
Invariant chain structure and MHC class II function [J].
Cresswell, P .
CELL, 1996, 84 (04) :505-507
[8]
ALLELE-SPECIFIC MOTIFS REVEALED BY SEQUENCING OF SELF-PEPTIDES ELUTED FROM MHC MOLECULES [J].
FALK, K ;
ROTZSCHKE, O ;
STEVANOVIC, S ;
JUNG, G ;
RAMMENSEE, HG .
NATURE, 1991, 351 (6324) :290-296
[9]
Antigen presentation and T cell development in H2-M-deficient mice [J].
FungLeung, WP ;
Surh, CD ;
Liljedahl, M ;
Pang, J ;
Leturcq, D ;
Peterson, PA ;
Webb, SR ;
Karlsson, L .
SCIENCE, 1996, 271 (5253) :1278-1281
[10]
Deficient positive selection of CD4 T cells in mice displaying altered repertoires of MHC class II-bound self-peptides [J].
Grubin, CE ;
Kovats, S ;
deRoos, P ;
Rudensky, AY .
IMMUNITY, 1997, 7 (02) :197-208