Cytokines in the oral mucosa of mice infected with Candida albicans

被引:22
作者
Farah, CS [1 ]
Gotjamanos, T
Seymour, GJ
Ashman, RB
机构
[1] Univ Queensland, Sch Dent, Brisbane, Qld 4072, Australia
[2] Univ Western Australia, Dept Pathol, QEII Med Ctr, Nedlands, WA 6009, Australia
来源
ORAL MICROBIOLOGY AND IMMUNOLOGY | 2002年 / 17卷 / 06期
关键词
cytokines; oral candidiasis; RT-PCR;
D O I
10.1034/j.1399-302X.2002.170607.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Oropharyngeal candidiasis is associated with defects in cell-mediated immunity, and is commonly seen in immunocompromised patients. We have previously shown that T-cell-deficient BALB/c nude (nu/nu) mice are extremely susceptible to oropharyngeal candidiasis, and that recovery from a chronic infection is dependent on CD4 T lymphocytes. In this study we describe the local tissue cytokine profile in lymphocyte-reconstituted immunodeficient mice and their euthymic counterparts. Mice were infected orally with 10(8) cells of the yeast Candida albicans , and oral tissues sampled on days 0, 4, 8, and 14. Nude mice were reconstituted with 3 x 10(7) naive lymphocytes following oral inoculation. Interleukin (IL)-6, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha were identified in the oral tissues of infected euthymic mice recovering from oral infection, as well as naive controls. TNF-alpha was identified in nude oral tissue on days 4 and 8, but only after lymphocyte reconstitution. No IL-2, IL-4 or IL-10 was detected in either euthymic or athymic mice at any time-point throughout the experiment. This study confirms the functional activity of T lymphocytes in reconstituted nude mice, and suggests that TNF-alpha may be an important mediator in the recovery from oropharyngeal candidiasis.
引用
收藏
页码:375 / 378
页数:4
相关论文
共 15 条
[1]  
AGGARWAL BB, 2000, CYTOKINE REFERENCE, P413, DOI DOI 10.1006/RWEY.2000.05001
[2]   INDUCTION OF TUMOR-NECROSIS-FACTOR-ALPHA IN MURINE CANDIDA-ALBICANS INFECTION [J].
ALLENDOERFER, R ;
MAGEE, DM ;
SMITH, JG ;
BONEWALD, L ;
GRAYBILL, JR .
JOURNAL OF INFECTIOUS DISEASES, 1993, 167 (05) :1168-1172
[3]  
CHEERS C, 1975, J IMMUNOL, V115, P844
[4]  
CLEVELAND WW, 1968, LANCET, V2, P1211
[5]   Primary role for CD4+ T lymphocytes in recovery from oropharyngeal candidiasis [J].
Farah, CS ;
Elahi, S ;
Drysdale, K ;
Pang, G ;
Gotjamanos, T ;
Seymour, GJ ;
Clancy, RL ;
Ashman, RB .
INFECTION AND IMMUNITY, 2002, 70 (02) :724-731
[6]   Irradiation-induced oral candidiasis in an experimental murine model [J].
Farah, CS ;
Hong, S ;
Wanasaengsakul, S ;
Elahi, S ;
Pang, G ;
Gotjamanos, T ;
Seymour, GJ ;
Clancy, RL ;
Ashman, RB .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2001, 16 (06) :358-363
[7]  
HOLUB M, 1971, ANN INTERN MED, V74, P955
[8]   ORAL CANDIDIASIS IN HIGH-RISK PATIENTS AS THE INITIAL MANIFESTATION OF THE ACQUIRED IMMUNODEFICIENCY SYNDROME [J].
KLEIN, RS ;
HARRIS, CA ;
SMALL, CB ;
MOLL, B ;
LESSER, M ;
FRIEDLAND, GH .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 311 (06) :354-358
[9]   Characterization of tumor necrosis factor-deficient mice [J].
Marino, MW ;
Dunn, A ;
Grail, D ;
Inglese, M ;
Noguchi, Y ;
Richards, E ;
Jungbluth, A ;
Wada, H ;
Moore, M ;
Williamson, B ;
Basu, S ;
Old, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :8093-8098
[10]   INVIVO CYTOKINE GENE-EXPRESSION IN T-CELL SUBSETS OF THE AUTOIMMUNE MRL/MP-LPR/LPR MOUSE [J].
MURRAY, LJ ;
LEE, R ;
MARTENS, C .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (01) :163-170