Expression of cytokine genes during pneumococcal and nontypeable Haemophilus influenzae acute otitis media in the rat

被引:69
作者
Melhus, Å
Ryan, AF
机构
[1] Univ Calif San Diego, Sch Med, Dept Surg Otolaryngol, La Jolla, CA 92093 USA
[2] Vet Affairs Med Ctr, La Jolla, CA USA
关键词
D O I
10.1128/IAI.68.7.4024-4031.2000
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Acute otitis media (AOM) elicits potent inflammatory responses from the cells of the middle ear mucosa as well as from infiltrating leukocytes, To explore host responses during experimental AOM induced by Streptococcus pneumoniae type 3 and nontypeable Haemophilus influenzae (NTHi), otomicroscopy findings and expression of cytokine genes in the middle ear were monitored up to 1 month postinoculation. The mucose and infiltrating cells responded rapidly to the bacterial challenge. Otomicroscopically, AOM appeared 1 day after NTHi inoculation and 3 days after pneumococcus inoculation. Pneumococcal AOM was more severe than NTHi otitis, but in general, lower transcript levels were detected in pneumococcus-infected than in NTHi-infected animals, Interleukin-6 (IL-6) mRNA levels peaked at 3 to 6 h for both pneumococcus-infected and NTHi-infected animals. IL-1 alpha, tumor necrosis factor alpha, and IL-10 mRNA levels peaked at 6 h for NTHi otitis and 1 to 3 days for pneumococcal otitis. Comparing otomicroscopy with expression profiles, it would appear that the majority of cytokine mRNAs had passed their peak before the AOM diagnosis could be made clinically. Only transforming growth factor beta mRNA followed a slower time course, peaking very late and continuing expression even after the AOM was otomicroscopically resolved. IL-2 and IL-4 mRNAs were not detected in any animal at any time. Most of the investigated cytokines are very early markers for AOM and may be involved in initiation of inflammation, but they would be poor targets for pharmacological manipulation since their levels decline before clinical signs appear.
引用
收藏
页码:4024 / 4031
页数:8
相关论文
共 41 条
[11]  
HAAKFRENDSCHO M, 1992, J IMMUNOL, V148, P3978
[12]   A MAP KINASE TARGETED BY ENDOTOXIN AND HYPEROSMOLARITY IN MAMMALIAN-CELLS [J].
HAN, J ;
LEE, JD ;
BIBBS, L ;
ULEVITCH, RJ .
SCIENCE, 1994, 265 (5173) :808-811
[13]   Upregulation of messenger RNA for inflammatory cytokines in middle ear mucosa in a rat model of acute otitis media [J].
Hebda, PA ;
Alper, CM ;
Doyle, WJ ;
Burckart, GJ ;
Diven, WF ;
Zeevi, A .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1998, 107 (06) :501-507
[14]   Serum interleukin-6 in bacterial and nonbacterial acute otitis media [J].
Heikkinen, T ;
Ghaffar, F ;
Okorodudu, AO ;
Chonmaitree, T .
PEDIATRICS, 1998, 102 (02) :296-299
[15]   Bacterial modulins: A novel class of virulence factors which cause host tissue pathology by inducing cytokine synthesis [J].
Henderson, B ;
Poole, S ;
Wilson, M .
MICROBIOLOGICAL REVIEWS, 1996, 60 (02) :316-+
[16]   A RAT MODEL FOR PNEUMOCOCCAL OTITIS-MEDIA [J].
HERMANSSON, A ;
EMGARD, P ;
PRELLNER, K ;
HELLSTROM, S .
AMERICAN JOURNAL OF OTOLARYNGOLOGY, 1988, 9 (03) :97-101
[17]  
HOWIE VM, 1985, PEDIATRICS, V75, P8
[18]   EARLY EXPRESSION OF CYTOKINE MESSENGER-RNA IN MICE INFECTED WITH LISTERIA-MONOCYTOGENES [J].
IIZAWA, Y ;
BROWN, JF ;
CZUPRYNSKI, CJ .
INFECTION AND IMMUNITY, 1992, 60 (10) :4068-4073
[19]   OTITIS-MEDIA [J].
KLEIN, JO .
CLINICAL INFECTIOUS DISEASES, 1994, 19 (05) :823-833
[20]   A simple nested RT-PCR method for quantitation of the relative amounts of multiple cytokine mRNAs in small tissue samples [J].
Kotake, S ;
Schumacher, HR ;
Wilder, RL .
JOURNAL OF IMMUNOLOGICAL METHODS, 1996, 199 (02) :193-203