CD4+ T cells and the proinflammatory cytokines gamma interferon and interleukin-6 contribute to alveolar bone loss in mice

被引:263
作者
Baker, PJ [1 ]
Dixon, M
Evans, RT
Dufour, L
Johnson, E
Roopenian, DC
机构
[1] Bates Coll, Dept Biol, Lewiston, ME 04240 USA
[2] SUNY Buffalo, Dept Oral Biol, Buffalo, NY 14214 USA
[3] Univ New England, Sch Dent Hyg, Portland, ME 04092 USA
[4] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
D O I
10.1128/IAI.67.6.2804-2809.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study, we used a mouse model to examine the role of the adaptive immune response in alveolar bone loss induced by oral infection with the human gram-negative anaerobic bacterium Porphyromonas gingivalis. Severe combined immunodeficient mice, which lack B and T lymphocytes, exhibited considerably less bone loss than did immunocompetent mice after oral infection, suggesting that lymphocytes contribute to this process. Bone loss after oral infection was decreased in mice deficient in major histocompatibility complex (MHC) class II-responsive CD4(+) T cells, but no change in bone loss was observed in mice deficient in MWC class I-responsive CD8(+) T cells or NK1(+) T cells. Mice lacking the cytokine gamma interferon or interleukin-6 also demonstrated decreased bone loss. These results suggest that the adaptive immune response, and in particular CD4(+) T cells and the proinflammatory cytokines that they secrete, are important effecters of bone loss consequent to P. gingivalis oral infection. The studies also reinforce the utility of the mouse oral infection model in dissecting the pathobiology of periodontal disease.
引用
收藏
页码:2804 / 2809
页数:6
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