Interleukin-1β-dependent changes in the hippocampus following parenteral immunization with a whole cell pertussis vaccine

被引:19
作者
Loscher, CE
Donnelly, S
Mills, KHG [1 ]
Lynch, MA
机构
[1] Natl Univ Ireland Maynooth, Dept Biol, Infect & Immun Grp, Maynooth, Kildare, Ireland
[2] Trinity Coll Dublin, Dept Physiol, Dublin 2, Ireland
关键词
pertussis vaccine; bacterial toxins; IL-1; beta; hippocampus; JNK;
D O I
10.1016/S0165-5728(00)00366-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neurological side effects are a major cause of concern following immunization with a number of vaccines, especially the whole cell pertussis vaccine (Pw). In this study we report that IL-1 beta concentrations were significantly increased in the hippocampus following subcutaneous (s.c.) injection of Pw, and that this was accompanied by increased activity of the stress-activated kinase, c-Jun-N-terminal kinase (JNK) and a decrease in glutamate release. These effects were mimicked by s.c injection of active pertussis toxin (PT) or lipopolysaccharide (LPS). Incubation of hippocampal synaptosomes in the presence of Pw, PT or LPS also resulted in increased JNK activation and decreased glutamate release, effects which were mimicked by IL-1 beta and blocked by the IL-I receptor antagonist (IL-ra). Our observations are consistent with the hypothesis that IL-1 beta induced by active bacterial toxins present in vaccine preparations, mediate the neurochemical and perhaps the neurological effects of Pw. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:68 / 76
页数:9
相关论文
共 63 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   Upregulation of Jun and Fos family members and permanent JNK activity lead to constitutive AP-1 activation in Theileria-transformed leukocytes [J].
Chaussepied, M ;
Lallemand, D ;
Moreau, MF ;
Adamson, R ;
Hall, R ;
Langsley, G .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1998, 94 (02) :215-226
[3]  
CHERRY J D, 1988, Pediatrics, V81, P939
[4]   CYCLOHEXIMIDE ABOLISHES PERTUSSIS TOXIN-INDUCED INCREASE IN GLUTAMATE RELEASE FROM CEREBELLAR GRANULE NEURONS [J].
CULLEN, GP ;
HUSTON, E ;
DOLPHIN, AC .
NEUROSCIENCE LETTERS, 1994, 166 (01) :17-22
[5]  
De Simoni MG, 1998, BIOL SIGNAL RECEPT, V7, P33
[6]   JNK1 - A PROTEIN-KINASE STIMULATED BY UV-LIGHT AND HA-RAS THAT BINDS AND PHOSPHORYLATES THE C-JUN ACTIVATION DOMAIN [J].
DERIJARD, B ;
HIBI, M ;
WU, IH ;
BARRETT, T ;
SU, B ;
DENG, TL ;
KARIN, M ;
DAVIS, RJ .
CELL, 1994, 76 (06) :1025-1037
[7]   Glycerol-induced seizure:: involvement of IL-1β and glutamate [J].
Donnelly, S ;
Loscher, C ;
Mills, KHG ;
Lynch, MA .
NEUROREPORT, 1999, 10 (09) :1821-1825
[8]   Differential activation of extracellular signal-regulated kinase (ERK) 1, ERK2, p38, and c-Jun NH2-terminal kinase mitogen-activated protein kinases by bacterial peptidoglycan [J].
Dziarski, R ;
Jin, YP ;
Gupta, D .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (04) :777-785
[9]   Bacterial endotoxin inhibits LHRH secretion following the increased release of hypothalamic GABA levels - Different effects on amino acid neurotransmitter release [J].
Feleder, C ;
Refojo, D ;
Jarry, H ;
Wuttke, W ;
Moguilevsky, JA .
NEUROIMMUNOMODULATION, 1996, 3 (06) :342-351
[10]   Effects of endotoxin on in vitro release of LHRH and amino acid neurotransmitters by preoptic mediobasal hypothalamic fragments [J].
Feleder, C ;
Jarry, H ;
Leonhardt, S ;
Moguilevsky, JA ;
Wuttke, W .
NEUROIMMUNOMODULATION, 1996, 3 (2-3) :76-81