REQUIREMENTS FOR THE GROWTH OF LYMPHOCYTE-TH1 CLONES

被引:29
作者
GERMANN, T
PARTENHEIMER, A
RUDE, E
机构
[1] Institut Für Immunologie, Johannes Gutenberg Universität, Mainz
关键词
D O I
10.1002/eji.1830200923
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Besides the signal generated in a T lymphocyte after triggering the T cell receptor (TcR), most lymphocytes need a “second signal” to become fully activated. The necessity and nature of the “second signal” differs between different types of T cells. At the level of CD4‐positive T helper lymphocytes interleukin 1 (IL 1) serves as “second signal” for those of the TH2 subtype (IL 4, 5, 6 producer) but not for those of the TH1 subtype (IL 2, IFN‐γ producer). This correlates with the absence of the IL 1 receptor at the surface of TH1 clones. We report herein the further purification of T cell stimulating factor (TSF), a soluble mediator involved in the proliferation of TH1 lymphocytes. A preparation free of detectable IL 1, 2, 4 and IL 6 activity could act as “second signal” required for the growth of TH1 lymphocytes in a TcR‐mediated, as well as a TcR‐independent activation system. In addition, we suggest that IL 1 can influence the proliferation of TH1 clones in an indirect way, probably via the induction of TSF in accessory cells. Copyright © 1990 Wiley‐VCH Verlag GmbH & Co. KGaA
引用
收藏
页码:2035 / 2040
页数:6
相关论文
共 32 条
[1]  
CANTRELL DA, 1983, J EXP MED, V158, P1859
[2]   HIGH ANTIGEN CONCENTRATION INHIBITS T-CELL PROLIFERATION BUT NOT INTERLEUKIN-2 PRODUCTION - EXAMINATION OF LIMITING DILUTION MICROCULTURES AND T-CELL CLONES [J].
CEREDIG, R ;
CORRADIN, G .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1986, 16 (01) :30-34
[3]   CHARACTERIZATION OF LYMPHOKINE-MEDIATED ACTIVATION OF MACROPHAGES FOR ANTIGEN PRESENTATION - STUDIES WITH LONG-TERM CULTURED BONE MARROW-DERIVED MACROPHAGES AND CLONED T-CELLS [J].
FISCHER, HG ;
RESKEKUNZ, AB ;
SPAETH, E ;
KIRCHNER, H ;
RUDE, E .
IMMUNOBIOLOGY, 1984, 168 (3-5) :232-245
[4]   INVOLVEMENT OF SOLUBLE MEDIATOR(S) DIFFERENT FROM INTERLEUKIN (IL) 1 IN THE ANTIGEN-INDUCED IL-2 RECEPTOR EXPRESSION AND PROLIFERATION OF L3T4+ (CD4+) LYMPHOCYTES-T [J].
GERMANN, T ;
SCHMITT, E ;
HUHN, H ;
RUDE, E .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (03) :459-465
[5]   AN ANTIGEN-INDEPENDENT PHYSIOLOGICAL ACTIVATION PATHWAY FOR L3T4+ LYMPHOCYTES-T [J].
GERMANN, T ;
HUHN, H ;
ZIMMERMANN, F ;
RUDE, E .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1987, 17 (06) :775-781
[6]   POTENTIATION OF T-LYMPHOCYTE RESPONSE TO MITOGENS .1. RESPONDING CELL [J].
GERY, I ;
GERSHON, RK ;
WAKSMAN, BH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1972, 136 (01) :128-&
[7]   PROCESSING REQUIREMENTS FOR THE RECOGNITION OF INSULIN FRAGMENTS BY MURINE T-CELLS [J].
GRADEHANDT, G ;
HAMPL, J ;
PLACHOV, D ;
RESKE, K ;
RUDE, E .
IMMUNOLOGICAL REVIEWS, 1988, 106 :59-75
[8]  
GREENBAUM LA, 1988, J IMMUNOL, V140, P1555
[9]   INTERLEUKIN-2 RECEPTOR BETA-CHAIN GENE - GENERATION OF 3 RECEPTOR FORMS BY CLONED HUMAN ALPHA-CHAIN AND BETA-CHAIN CDNAS [J].
HATAKEYAMA, M ;
TSUDO, M ;
MINAMOTO, S ;
KONO, T ;
DOI, T ;
MIYATA, T ;
MIYASAKA, M ;
TANIGUCHI, T .
SCIENCE, 1989, 244 (4904) :551-556
[10]   ACTIVATION OF RESTING LYMPHOCYTES-T BY CROSS-LINKED ANTI-CD3 (T3) [J].
HEUMANN, D ;
VISCHER, TL .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1987, 17 (11) :1657-1660