IL-4 production by allergen-stimulated primary cultures: Identification of basophils as the major IL-4-producing cell type

被引:35
作者
Kasaian, MT
Clay, MJ
Happ, MP
Garman, RD
Hirani, S
Luqman, M
机构
[1] ImmuLogic Pharmaceutical Corp., Waltham, MA 02154
关键词
atopy; cytokines; T cell;
D O I
10.1093/intimm/8.8.1287
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As a potent inducing agent for IgE production and differentiation factor for allergen-specific T(h)2 cells, IL-4 is a key regulatory cytokine both in the pathogenesis of allergic disease and in the ongoing allergic response, The assay of in vitro IL-4 production has often been used to compare the allergen responses of T cells isolated from atopic and non-atopic subjects, Because peripheral blood basophils also have the capacity to respond to specific allergen by producing IL-4, we investigated the relative contribution of these two cell types to IL-4 production in allergen-stimulated primary cultures, Among unfractionated peripheral blood mononuclear cells (PBMC), the major producers of detectable IL-4 in primary in vitro cultures were found to be basophils based on: (i) an allergen dose-response corresponding closely to that required for basophil histamine release and lower than that required for T cell activation; (ii) a rapid time course for IL-4 production (detectable st 3 h), inconsistent with the typical activation requirements of fresh T cells; (iii) the production of comparable levels of IL-4 in cultures stimulated with allergen or anti-IgE; and (iv) the complete loss of detectable IL-4 production following specific depletion of basophils from PBMC, The T cells in these cultures were functionally able to produce IL-4, as demonstrated by mitogen activation of basophil-depleted PBMC, These findings demonstrate that although IL-4 production in primary in vitro cultures can be used as a sensitive indicator of allergen responsiveness, the accurate interpretation of this result requires identification of the responding cell type, Furthermore, these findings raise the possibility that basophil production of IL-4 early in the course of allergen stimulation may shape subsequent T cell responses both in vivo and in vitro.
引用
收藏
页码:1287 / 1297
页数:11
相关论文
共 42 条
[1]  
AROCK M, 1993, J IMMUNOL, V151, P1441
[2]  
BRADDING P, 1993, J IMMUNOL, V151, P3853
[3]   INTERLEUKIN-4 IS LOCALIZED TO AND RELEASED BY HUMAN MAST-CELLS [J].
BRADDING, P ;
FEATHER, IH ;
HOWARTH, PH ;
MUELLER, R ;
ROBERTS, JA ;
BRITTEN, K ;
BEWS, JPA ;
HUNT, TC ;
OKAYAMA, Y ;
HEUSSER, CH ;
BULLOCK, GR ;
CHURCH, MK ;
HOLGATE, ST .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (05) :1381-1386
[4]  
BRINKMANN V, 1995, J IMMUNOL, V154, P3078
[5]   HUMAN PERIPHERAL-BLOOD BASOPHILS PRIMED BY INTERLEUKIN-3 (IL-3) PRODUCE IL-4 IN RESPONSE TO IMMUNOGLOBULIN-E-RECEPTOR STIMULATION [J].
BRUNNER, T ;
HEUSSER, CH ;
DAHINDEN, CA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (03) :605-611
[6]   FREQUENCY OF ALLERGEN-SPECIFIC T-LYMPHOCYTES IN BLOOD AND BRONCHIAL RESPONSE TO ALLERGEN IN ASTHMA [J].
BURASTERO, SE ;
FENOGLIO, D ;
CRIMI, E ;
BRUSASCO, V ;
ROSSI, GA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1993, 91 (05) :1075-1081
[7]  
CHAPMAN MD, 1988, J IMMUNOL, V140, P812
[8]   CUTANEOUS LATE-PHASE RESPONSE TO ALLERGEN - MEDIATOR RELEASE AND INFLAMMATORY CELL INFILTRATION [J].
CHARLESWORTH, EN ;
HOOD, AF ;
SOTER, NA ;
KAGEYSOBOTKA, A ;
NORMAN, PS ;
LICHTENSTEIN, LM .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (05) :1519-1526
[9]   LATE-PHASE AIRWAY REACTION AND INFLAMMATION [J].
DOLOVICH, J ;
HARGREAVE, FE ;
JORDANA, M ;
DENBURG, J .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 83 (02) :521-524
[10]  
EBNER C, 1995, J IMMUNOL, V154, P1932