Opioid receptor blockade increases the number of lymphocytes without altering T cell response in draining lymph nodes in vivo

被引:20
作者
Jaume, Martial
Laffont, Sophie
Chapey, Emmanuelle
Blanpied, Catherine
Dietrich, Gilles [1 ]
机构
[1] INSERM, U563, Ctr Physiopathol Toulouse Purpan, F-31300 Toulouse, France
[2] Univ Toulouse III Paul Sabatier, Inst Claude Preval, F-31400 Toulouse, France
关键词
Opioids; CD4(+) T cells; cell proliferation; lymph nodes; mice;
D O I
10.1016/j.jneuroim.2007.06.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A number of studies have been dedicated to estimate the consequences on immunity of the clinical use of opioids by focusing on mitogen-induced polyclonal proliferation of T cells from blood or spleen. Here we examined, under physiological conditions, the contribution of endogenous opioids in the development of a CD4(+) T cell response within draining lymph nodes. We show in OVA-primed DOI 11.10 mice that delta-opioid receptors were upregulated upon Tcell activation in vivo and that opioid receptor neutralization increased the number of specific anti-OVAT lymphocytes without promoting their capacity to proliferate. The sensitivity to Fas-mediated apoptosis of T lymphocytes and the synthesis of homeostatic lymphoid chernokines were not either affected suggesting that opioids operate mainly before the entry of T lymphocytes into lymph nodes. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:95 / 102
页数:8
相关论文
共 44 条
[1]   MORPHINE-INHIBITION OF LYMPHOCYTE ACTIVITY IS MEDIATED BY AN OPIOID DEPENDENT MECHANISM [J].
BAYER, BM ;
DAUSSIN, S ;
HERNANDEZ, M ;
IRVIN, L .
NEUROPHARMACOLOGY, 1990, 29 (04) :369-374
[2]   Dynamics of CD8+ T cell priming by dendritic cells in intact lymph nodes [J].
Bousso, P ;
Robey, E .
NATURE IMMUNOLOGY, 2003, 4 (06) :579-585
[3]  
BRYANT HU, 1988, J PHARMACOL EXP THER, V245, P913
[4]   Chemokines in tissue-specific and microenvironment-specific lymphocyte homing [J].
Campbell, JJ ;
Butcher, EC .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (03) :336-341
[5]   Opioid modulation of immune responses: effects on phagocyte and lymphoid cell populations [J].
Eisenstein, TK ;
Hilburger, ME .
JOURNAL OF NEUROIMMUNOLOGY, 1998, 83 (1-2) :36-44
[6]   Murine dendritic cells express functional delta-type opioid receptors [J].
Esche, C ;
Makarenkova, VP ;
Kost, NV ;
Lotze, MT ;
Zozulya, AA ;
Shurin, MR .
CUTANEOUS NEUROIMMUNOMODULATION: THE PROOPIOMELANOCORTIN SYSTEM, 1999, 885 :387-390
[7]   RESTRAINT STRESS-INDUCED ELEVATIONS IN PLASMA-CORTICOSTERONE AND BETA-ENDORPHIN ARE NOT ACCOMPANIED BY ALTERATIONS IN IMMUNE FUNCTION [J].
FLORES, CM ;
HERNANDEZ, MC ;
HARGREAVES, KM ;
BAYER, BM .
JOURNAL OF NEUROIMMUNOLOGY, 1990, 28 (03) :219-225
[8]  
FLORES LR, 1994, J PHARMACOL EXP THER, V268, P1129
[9]   CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs [J].
Förster, R ;
Schubel, A ;
Breitfeld, D ;
Kremmer, E ;
Renner-Müller, I ;
Wolf, E ;
Lipp, M .
CELL, 1999, 99 (01) :23-33
[10]   Interleukin 4-producing CD4 T cells arise from different precursors depending on the conditions of antigen exposure in vivo [J].
Foucras, G ;
Gapin, L ;
Coureau, C ;
Kanellopoulos, JM ;
Guéry, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (04) :683-693