Development of hapten-induced IL-4-producing CD4+ T lymphocytes requires early IL-4 production by αβ T lymphocytes carrying invariant Vα14 TCR α chains

被引:15
作者
Dieli, F
Taniguchi, M
Asherson, GL
Sireci, G
Caccamo, N
Scirè, E
Bonanno, CT
Salerno, A
机构
[1] Univ Palermo, Inst Gen Pathol, I-90134 Palermo, Italy
[2] CNR, ISMEDA, Immunopathol Sect, I-90134 Palermo, Italy
[3] Chiba Univ, Ctr Biomed Sci, Div Mol Immunol, Chiba 260, Japan
[4] Wellcome Inst Hist Med Sci, Twentieth Century Hist Med, London NW1 2BE, England
基金
英国惠康基金;
关键词
haptens; IL-4; T(h)2 response; V(alpha)14(+) T cells;
D O I
10.1093/intimm/10.4.413
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This paper investigates the mechanisms responsible for the generation of IL-4-producing CD4(+) T cells during contact sensitization with the hapten trinitrochlorobenzene (TNCB). Lymph node cells taken 1 day after immunization spontaneously released IL-4 while lymph node cells taken 2 and 3 days after immunization did not produce IL-4, A second wave of IL-4 production that was both antigen-specific and MHC class II (I-A)-restricted was observed 4 days after immunization. The spontaneous release of IL-4 at day 1 was due to the alpha beta(+) double-negative (CD4(-)CD8(-)) T lymphocytes that also expressed NK1.1 and showed V(alpha)14 rearrangement, while alpha beta(+) CD4(+) T lymphocytes were the source of the antigen-specific IL-4 production at day 4. Early IL-4 production was required for the development of IL-4-producing CD4(+) T cells as mice injected with anti-V(alpha)14 or anti-IL-4 mAb produced little IL-4 and IL-10, while production of IFN-gamma was increased similar to 2-fold. These results indicate that the development of IL-4-producing CD4(+) T lymphocytes in the TNCB system requires early production of IL-4 by alpha beta(+) double-negative cells carrying invariant V(alpha)14 TCR alpha chain.
引用
收藏
页码:413 / 420
页数:8
相关论文
共 51 条
[11]  
DIELI F, 1996, INT IMMUNOL, V8, P101
[12]   Interleukin-4-producing CD4(+) NK1.1(+) TCR alpha/beta(intermediate) liver lymphocytes are downregulated by Listeria monocytogenes [J].
Emoto, M ;
Emoto, Y ;
Kaufmann, SHE .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (12) :3321-3325
[13]  
ENK AH, 1993, J IMMUNOL, V151, P2184
[14]  
FOWLKERS BJ, 1987, NATURE, V329, P332
[15]  
GAJEWSKI TF, 1989, J IMMUNOL, V143, P15
[16]  
GREENBAUM LA, 1988, J IMMUNOL, V140, P1555
[17]  
HOPE JC, 1994, IMMUNOLOGY, V83, P250
[18]   MONOCLONAL-ANTIBODY AGAINST MURINE T-CELL RECEPTOR V-ALPHA-14 CROSS-REACTS WITH HUMAN CD3-EPSILON AND DETECTS DISULFIDE-LINKED DIMERIC FORM [J].
ITO, T ;
ISHIBASHI, K ;
IMAI, K ;
KOSEKI, H ;
RA, C ;
FERNANDEZ, E ;
KANTAKE, M ;
SAITO, T ;
TANIGUCHI, M .
INTERNATIONAL IMMUNOLOGY, 1991, 3 (10) :991-995
[19]   ESTABLISHMENT OF MOUSE-CELL LINES WHICH CONSTITUTIVELY SECRETE LARGE QUANTITIES OF INTERLEUKIN-2, INTERLEUKIN-3, INTERLEUKIN-4 OR INTERLEUKIN-5, USING MODIFIED CDNA EXPRESSION VECTORS [J].
KARASUYAMA, H ;
MELCHERS, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (01) :97-104
[20]   MAC1 DISCRIMINATES UNUSUAL CD4(-)CD8(-) DOUBLE-NEGATIVE T-CELLS BEARING ALPHA-BETA ANTIGEN RECEPTOR FROM CONVENTIONAL ONES WITH EITHER CD4 OR CD8 IN MURINE LUNG [J].
KAWAKAMI, K ;
TERUYA, K ;
TOHYAMA, M ;
KUDEKEN, N ;
YONAMINE, Y ;
SAITO, R .
IMMUNOLOGY LETTERS, 1995, 46 (1-2) :143-152