The anatomy of T-cell activation and tolerance

被引:168
作者
Mondino, A [1 ]
Khoruts, A [1 ]
Jenkins, MK [1 ]
机构
[1] UNIV MINNESOTA, SCH MED, CTR IMMUNOL, MINNEAPOLIS, MN 55455 USA
关键词
D O I
10.1073/pnas.93.6.2245
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mammalian immune system must specifically recognize and eliminate foreign invaders but refrain from damaging the host. This task is accomplished in part by the production of a large number of T lymphocytes, each bearing a different antigen receptor to match the enormous variety of antigens present in the microbial world. However, because antigen receptor diversity is generated by a random mechanism, the immune system must tolerate the function of T lymphocytes that by chance express a self-reactive antigen receptor. Therefore, during early development, T cells that are specific for antigens expressed in the thymus are physically deleted. The population of T cells that leaves the thymus and seeds the secondary lymphoid organs contains helpful cells that are specific for antigens from microbes but also potentially dangerous T cells that are specific for innocuous extrathymic self antigens. The outcome of an encounter by a peripheral T cell with these two types of antigens is to a great extent determined by the inability of naive T cells to enter nonlymphoid tissues or to be productively activated in the absence of inflammation.
引用
收藏
页码:2245 / 2252
页数:8
相关论文
共 113 条
[71]   TOLERANCE, DANGER, AND THE EXTENDED FAMILY [J].
MATZINGER, P .
ANNUAL REVIEW OF IMMUNOLOGY, 1994, 12 :991-1045
[72]   DOES T-CELL TOLERANCE REQUIRE A DEDICATED ANTIGEN-PRESENTING CELL [J].
MATZINGER, P ;
GUERDER, S .
NATURE, 1989, 338 (6210) :74-76
[73]   EXAGGERATED AND PERSISTENT CUTANEOUS DELAYED-TYPE HYPERSENSITIVITY IN TRANSGENIC MICE WHOSE EPIDERMAL-KERATINOCYTES CONSTITUTIVELY EXPRESS B7-1 ANTIGEN [J].
NASIR, A ;
FERBEL, B ;
SALMINEN, W ;
BARTH, RK ;
GASPARI, AA .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) :892-898
[74]   THE TRANSCAPSULAR ROUTE - A NEW WAY FOR (SELF-) ANTIGENS TO BYPASS THE BLOOD-THYMUS BARRIER [J].
NIEUWENHUIS, P ;
STET, RJM ;
WAGENAAR, JPA ;
WUBBENA, AS ;
KAMPINGA, J ;
KARRENBELD, A .
IMMUNOLOGY TODAY, 1988, 9 (12) :372-375
[75]   A 39-KDA PROTEIN ON ACTIVATED HELPER T-CELLS BINDS CD40 AND TRANSDUCES THE SIGNAL FOR COGNATE ACTIVATION OF B-CELLS [J].
NOELLE, RJ ;
ROY, M ;
SHEPHERD, DM ;
STAMENKOVIC, I ;
LEDBETTER, JA ;
ARUFFO, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6550-6554
[76]   ABLATION OF TOLERANCE AND INDUCTION OF DIABETES BY VIRUS-INFECTION IN VIRAL-ANTIGEN TRANSGENIC MICE [J].
OHASHI, PS ;
OEHEN, S ;
BUERKI, K ;
PIRCHER, H ;
OHASHI, CT ;
ODERMATT, B ;
MALISSEN, B ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
CELL, 1991, 65 (02) :305-317
[77]   SURVIVAL OF MOUSE PANCREATIC-ISLET ALLOGRAFTS IN RECIPIENTS TREATED WITH ALLOGENEIC SMALL LYMPHOCYTES AND ANTIBODY TO CD40 LIGAND [J].
PARKER, DC ;
GREINER, DL ;
PHILLIPS, NE ;
APPEL, MC ;
STEELE, AW ;
DURIE, FH ;
NOELLE, RJ ;
MORDES, JP ;
ROSSINI, AA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (21) :9560-9564
[78]  
Picker Louis J., 1993, P145
[79]   T-CELLS IN INFLAMMATORY BOWEL-DISEASE - PROTECTIVE AND PATHOGENIC ROLES [J].
POWRIE, F .
IMMUNITY, 1995, 3 (02) :171-174
[80]   SOLUBLE-ANTIGEN CAN CAUSE ENHANCED APOPTOSIS OF GERMINAL-CENTER B-CELLS [J].
PULENDRAN, B ;
KANNOURAKIS, G ;
NOURI, S ;
SMITH, KGC ;
NOSSAL, GJV .
NATURE, 1995, 375 (6529) :331-334