Immunization of Macaca fascicularis against experimental periodontitis using a vaccine containing cysteine proteases purified from Porphyromonas gingivalis

被引:41
作者
Page, R. C.
Lantz, M. S.
Darveau, R.
Jeffcoat, M.
Mancl, L.
Houston, L.
Braham, P.
Persson, G. R.
机构
[1] Univ Washington, Sch Dent, Dept Dent Publ Hlth Sci, Seattle, WA 98195 USA
[2] Indiana Univ, Dept Periodont, Indianapolis, IN 46204 USA
[3] Indiana Univ, Reg Clin Dent Res Ctr, Indianapolis, IN 46204 USA
[4] Indiana Univ, Dept Oral Biol, Sch Dent, Indianapolis, IN 46204 USA
[5] Univ Alabama Birmingham, Sch Dent, Dept Periodont, Birmingham, AL 35294 USA
来源
ORAL MICROBIOLOGY AND IMMUNOLOGY | 2007年 / 22卷 / 03期
关键词
alveolar bone loss; cysteine protease; periodontitis; Porphyromonas gingivalis; serum antibodies; vaccine;
D O I
10.1111/j.1399-302X.2007.00337.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: Periodontitis is a common infectious disease to which Porphyromonas gingivalis has been closely linked, in which the attachment tissues of the teeth and their alveolar bone housing are destroyed. We conducted a study to determine if immunization using a purified antigen could alter the onset and progression of the disease. Methods: Using the ligature-induced model of periodontitis in Macaca fascicularis, we immunized five animals with cysteine protease purified from P. gingivalis and used an additional five animals as controls. Alveolar bone loss was measured by digital subtraction radiography. Results: Immunization induced high titers of specific immunoglobuin G serum antibodies that were opsonic. Total bacterial load, levels of P. gingivalis in subgingival plaque and levels of prostaglandin E-2 in gingival crevicular fluid were significantly reduced. Onset and progression of alveolar bone loss was inhibited by approximately 50%. No manifestations of toxicity were observed. Conclusions: Immunization using a purified protein antigen from P. gingivalis inhibits alveolar bone destruction in a ligature-induced periodontitis model in M. fascicularis.
引用
收藏
页码:162 / 168
页数:7
相关论文
共 61 条
[1]   Destructive periodontal disease in adults 30 years of age and older in the United states, 1988-1994 [J].
Albandar, JM ;
Brunelle, JA ;
Kingman, A .
JOURNAL OF PERIODONTOLOGY, 1999, 70 (01) :13-29
[2]   AN ADJUVANT FORMULATION THAT SELECTIVELY ELICITS THE FORMATION OF ANTIBODIES OF PROTECTIVE ISOTYPES AND OF CELL-MEDIATED-IMMUNITY [J].
ALLISON, AC ;
BYARS, NE .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 95 (02) :157-168
[3]  
American Academy of Periodontology, 2000, J PERIODONTOL, V71, P847
[4]   Serum antibodies to Porphyromonas gingivalis block the prostaglandin E-2 response to lipopolysaccharide by mononuclear cells [J].
Bainbridge, BW ;
Page, RC ;
Darveau, RP .
INFECTION AND IMMUNITY, 1997, 65 (11) :4801-4805
[5]   ORAL INFECTION WITH PORPHYROMONAS-GINGIVALIS AND INDUCED ALVEOLAR BONE LOSS IN IMMUNOCOMPETENT AND SEVERE COMBINED IMMUNODEFICIENT MICE [J].
BAKER, PJ ;
EVANS, RT ;
ROOPENIAN, DC .
ARCHIVES OF ORAL BIOLOGY, 1994, 39 (12) :1035-1040
[6]   Passive immunization with monoclonal antibodies against Porphyromonas gingivalis in patients with periodontitis [J].
Booth, V ;
Ashley, FP ;
Lehner, T .
INFECTION AND IMMUNITY, 1996, 64 (02) :422-427
[7]   Prevalence and trends in periodontitis in the USA: from the NHANES III to the NHANES, 1988 to 2000 [J].
Borrell, LN ;
Burt, BA ;
Taylor, GW .
JOURNAL OF DENTAL RESEARCH, 2005, 84 (10) :924-930
[8]   The economics of periodontal diseases [J].
Brown, LJ ;
Johns, BA ;
Wall, TP .
PERIODONTOLOGY 2000, 2002, 29 :223-234
[9]   HUMORAL IMMUNE-RESPONSES TO PORPHYROMONAS-GINGIVALIS BEFORE AND FOLLOWING THERAPY IN RAPIDLY PROGRESSIVE PERIODONTITIS PATIENTS [J].
CHEN, HA ;
JOHNSON, BD ;
SIMS, TJ ;
DARVEAU, RP ;
MONCLA, BJ ;
WHITNEY, CW ;
ENGEL, D ;
PAGE, RC .
JOURNAL OF PERIODONTOLOGY, 1991, 62 (12) :781-791
[10]   Capsular polysaccharide-fimbrial protein conjugate vaccine protects against Porphyromonas gingivalis infection in SCID mice reconstituted with human peripheral blood lymphocytes [J].
Choi, JI ;
Schifferle, RE ;
Yoshimura, F ;
Kim, BW .
INFECTION AND IMMUNITY, 1998, 66 (01) :391-393