EXTRATHYMIC T-CELL DIFFERENTIATION

被引:122
作者
ROCHA, B
GUYGRAND, D
VASSALLI, P
机构
[1] UNIV GENEVA,CTR MED,DEPT PATHOL,CH-1211 GENEVA 4,SWITZERLAND
[2] HOP NECKER ENFANTS MALAD,INSERM,U429,F-75743 PARIS 15,FRANCE
关键词
D O I
10.1016/0952-7915(95)80008-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the mouse, the gut mucosa is a major site of extrathymic differentiation of T cells. Recent data in this past year show that this process differs from the main thymic differentiation pathway not only in its location, but also in its use of costimulatory molecules, signal transduction modules, and mechanisms of repertoire selection. The thymus exerts an influence on the expansion of the extrathymically differentiated gut intraepithelial lymphocytes that appears to be varied in nature, including acting as a source of TCR(-) progenitors. All gut intraepithelial lymphocytes, whatever their extrathymic or thymic site of differentiation, have common features of activated and specialized cytotoxic cells. Other T cells may differentiate extrathymically, in particular in the liver; these later cells appear to have a very restricted, probably autoreactive repertoire, and also display natural killer cell features.
引用
收藏
页码:235 / 242
页数:8
相关论文
共 55 条
[21]   CD3(+)CD16(+)NK1.1(+)B220(+) LARGE GRANULAR LYMPHOCYTES ARISE FROM BOTH ALPHA-BETA-TCR(+)CD4(-)CD8(-) AND GAMMA-DELTA-TCR(+)CD4(-)CD8(-) CELLS [J].
KOYASU, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (06) :1957-1972
[22]   AN INVARIANT T-CELL RECEPTOR-ALPHA CHAIN IS USED BY A UNIQUE SUBSET OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I-SPECIFIC CD4+ AND CD4-8- T-CELLS IN MICE AND HUMANS [J].
LANTZ, O ;
BENDELAC, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) :1097-1106
[23]   DEVELOPMENTAL EXPRESSION OF THE ALPHA(IEL)BETA(7) INTEGRIN ON T-CELL RECEPTOR-GAMMA-DELTA AND T-CELL RECEPTOR-ALPHA-BETA T-CELLS [J].
LEFRANCOIS, L ;
BARRETT, TA ;
HAVRAN, WL ;
PUDDINGTON, L .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (03) :635-640
[24]  
LEFRANCOIS L, 1994, J IMMUNOL, V153, P987
[25]   PROGENIES OF FETAL THYMOCYTES ARE THE MAJOR SOURCE OF CD4-CD8+ALPHA-ALPHA INTESTINAL INTRAEPITHELIAL LYMPHOCYTES EARLY IN ONTOGENY [J].
LIN, T ;
MATSUZAKI, G ;
KENAI, H ;
NOMOTO, K .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (08) :1785-1791
[26]  
LIN T, 1993, EUR J IMMUNOL, V2, P1968
[27]   CHARACTERISTICS OF FETAL THYMUS-DERIVED T-CELL RECEPTOR-GAMMA-DELTA INTESTINAL INTRAEPITHELIAL LYMPHOCYTES [J].
LIN, TS ;
MATSUZAKI, G ;
KENAI, H ;
KISHIHARA, K ;
NABESHIMA, S ;
FUNGLEUNG, WP ;
MAK, TW ;
NOMOTO, K .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (08) :1792-1798
[28]   ABNORMAL T-CELL DEVELOPMENT IN CD3-ZETA-/- MUTANT MICE AND IDENTIFICATION OF A NOVEL T-CELL POPULATION IN THE INTESTINE [J].
LIU, CP ;
UEDA, R ;
SHE, JA ;
SANCHO, J ;
WANG, BP ;
WEDDELL, G ;
LORING, J ;
KURAHARA, C ;
DUDLEY, EC ;
HAYDAY, A ;
TERHORST, C ;
HUANG, M .
EMBO JOURNAL, 1993, 12 (12) :4863-4875
[29]  
LYNCH S, 1995, IN PRESS EUR J IMMUN
[30]   EXTRATHYMIC DEVELOPMENT OF V-ALPHA-14-POSITIVE T-CELLS [J].
MAKINO, Y ;
YAMAGATA, N ;
SASHO, T ;
ADACHI, Y ;
KANNO, R ;
KOSEKI, H ;
KANNO, M ;
TANIGUCHI, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (05) :1399-1408