IL-7 enhances Ag-specific human T cell response by increasing expression of IL-2R α and γ chains

被引:20
作者
Chou, YK
Bourdette, DN
Barnes, D
Finn, TP
Murray, S
Unsicker, L
Robey, I
Whitham, RH
Buenafe, AC
Allegretta, M
Offner, H
Vandenbark, AA
机构
[1] Vet Affairs Med Ctr, Serv Neurol, Portland, OR 97201 USA
[2] Oregon Hlth Sci Univ, Dept Neurol, Portland, OR 97201 USA
[3] Connet Corp, Palo Alto, CA 94303 USA
[4] Oregon Hlth Sci Univ, Dept Mol Microbiol & Immunol, Portland, OR 97201 USA
关键词
IL-7; IL-2R; human T cells; survival factor;
D O I
10.1016/S0165-5728(99)00002-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin-7 has demonstrated potent enhancing effects on the growth and differentiation of several immature cell types, including thymocytes, and on survival of resting and antigen activated T cells. In this study, we evaluated the effects of IL-7 on post-thymic antigen-specific T cells from human blood. IL-7 was found to enhance proliferation responses and IFN-gamma secretion of myelin or recall Ag-specific Th1 cells through the selective up-regulation of the IL-2R alpha and gamma but not beta chains in both an Ag-dependent and Ag-independent manner, but did not affect monocytes, B cells, or NK cells. These functions of IL-7 enhanced the detection of Th1 but not Th2 cell frequency by > 2.5 fold, and promoted selection of kg-specific Th1 cells by the limiting dilution method. Moreover, IL-7 pretreatment conferred increased resistance of CD4 + T cells to CD8 + cell lysis, These studies demonstrate that IL-7 promotes the growth and survival of circulating Ag-specific human Th1 cells through a mechanism that probably involves the gamma c common receptor for IL-2 family members that includes IL-7. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:101 / 111
页数:11
相关论文
共 44 条
[1]  
ARMANT M, 1995, IMMUNOLOGY, V85, P331
[2]  
ARMITAGE RJ, 1990, J IMMUNOL, V144, P938
[3]   DIFFERENTIAL FUNCTION OF MAJOR HISTOCOMPATIBILITY COMPLEX ANTIGENS IN T-LYMPHOCYTE ACTIVATION [J].
BACH, FH ;
BACH, ML ;
SONDEL, PM .
NATURE, 1976, 259 (5541) :273-281
[4]  
BOURDETTE DN, 1994, J IMMUNOL, V152, P2510
[5]   PREVENTION OF T-CELL ANERGY BY SIGNALING THROUGH THE GAMMA(C) CHAIN OF THE IL-2 RECEPTOR [J].
BOUSSIOTIS, VA ;
BARBER, DL ;
NAKARAI, T ;
FREEMAN, GJ ;
GRIBBEN, JG ;
BERNSTEIN, GM ;
DANDREA, AD ;
RITZ, J ;
NADLER, LM .
SCIENCE, 1994, 266 (5187) :1039-1042
[6]   INTERLEUKIN-7 IS A T-CELL GROWTH-FACTOR [J].
CHAZEN, GD ;
PEREIRA, GMB ;
LEGROS, G ;
GILLIS, S ;
SHEVACH, EM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) :5923-5927
[7]  
Chou YK, 1996, J NEUROSCI RES, V45, P838, DOI 10.1002/(SICI)1097-4547(19960915)45:6<838::AID-JNR21>3.0.CO
[8]  
2-Q
[9]   FREQUENCY OF T-CELLS SPECIFIC FOR MYELIN BASIC-PROTEIN AND MYELIN PROTEOLIPID PROTEIN IN BLOOD AND CEREBROSPINAL-FLUID IN MULTIPLE-SCLEROSIS [J].
CHOU, YK ;
BOURDETTE, DN ;
OFFNER, H ;
WHITHAM, R ;
WANG, RY ;
HASHIM, GA ;
VANDENBARK, AA .
JOURNAL OF NEUROIMMUNOLOGY, 1992, 38 (1-2) :105-113
[10]  
CONLON DM, 1989, EUR J IMMUNOL, V19, P783