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Infection and Immunity, February 2004, p. 1166-1168, Vol. 72, No. 2
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.2.1166-1168.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Periodontitis Vaccine Decreases Local Prostaglandin E₂ Levels in a Primate Model

Frank A. Roberts,^1* Laura S. Houston,¹ Sheila A. Lukehart,² Lloyd A. Mancl,³ G. Rutger Persson,¹ and Roy C. Page¹

Departments of Periodontics,¹ Medicine,² Dental Public Health Sciences, University of Washington, Seattle, Washington 98195³

Received 28 July 2003/ Returned for modification 15 September 2003/ Accepted 10 November 2003

Top Abstract Introduction References

 
Interleukin-1ß, tumor necrosis factor alpha, prostaglandin E₂ (PGE₂), and Porphyromonas gingivalis-specific immunoglobulin G levels in gingival crevicular fluid were measured in primates immunized with a P. gingivalis vaccine followed by ligature-induced periodontitis. Only PGE₂ levels were dramatically suppressed (P < 0.0001) in immunized animals versus controls. A significant correlation (P < 0.027) was also found between PGE₂ levels and decreased bone loss scores. This study presents the first evidence of a potential mechanism involved in periodontitis vaccine-induced suppression of bone loss in a nonhuman primate model and offers insight into the role of PGE₂ in periodontal destruction.

Top Abstract Introduction References

 
Periodontitis is a chronic inflammatory condition that can result in tooth loss due to bone and tissue destruction. This disease is associated with pathogenic gram-negative bacteria, such as Porphyromonas gingivalis (4, 9, 13). The mechanisms by which P. gingivalis promotes periodontitis are still incompletely understood, although lipopolysaccharide (LPS) has been implicated. Bacterial LPS is a potent stimulator of many inflammatory mediators, including interleukin-1 beta (IL-1ß), tumor necrosis factor alpha (TNF-), and prostaglandin E₂ (PGE₂) (3, 5, 14), each of which is elevated in the nonhuman primate model of ligature-induced periodontitis (7, 10-12). The specific role of these mediators has yet to be determined, but local production of inflammatory mediators in the gingiva has been hypothesized to cause osteoclast activation and the resultant bone resorption that defines periodontitis. We previously reported that immunization of Macaca fascicularis monkeys with formalin-killed P. gingivalis resulted in less bone loss than in nonimmunized control animals in the ligature-induced periodontitis model (15). The mechanism for this protection was not determined, however. Therefore, this study examined the levels of IL-1ß, TNF-, PGE₂, and P. gingivalis-specific immunoglobulin G (IgG) antibodies in the gingival crevicular fluid (GCF) from immunized versus nonimmunized macaques.

Ten M. fascicularis monkeys were immunized at weeks 0, 3, 6, and 16 with formalin-killed P. gingivalis strain 5083 in SAF adjuvant (Syntex Laboratories, Palo Alto, Calif.), while 10 control monkeys were injected with adjuvant only (15). Ligatures were placed subgingivally around the second premolar and first and second molar teeth in one mandibular and one contralateral maxillary posterior sextant in each animal. GCF was collected with paper strips (ProFlow, Inc., Amityville, N.Y.) from the sulcus or pocket of two maxillary (nonligated) and two mandibular ligated posterior teeth on the same side at each visit during the study. Mediator and antibody assays were performed on GCF samples collected at weeks 20 and 36, corresponding with bone height measurement points. A series of sequential enzyme-linked immunosorbent assays (ELISAs) were performed with the GCF samples. First, human IL-1ß was measured by ELISA according to the kit's instructions (Cistron, Pinebrook, N.J.). A 100-µl aliquot of sample or standard was added to an IL-1ß-precoated microtiter plate, and after the initial incubation, the sample was then transferred to a TNF- ELISA assay plate (Genzyme, Cambridge, Mass.) and finally to an anti-P.gingivalis ELISA plate (6). An additional GCF aliquot was used to quantitate PGE₂ in a competitive inhibition assay conducted according to the manufacturer's instructions (Amersham, Arlington Heights, Ill.). IL-1ß, TNF-, and PGE₂ assays were read at an optical density at 450 nm (OD₄₅₀) on a microplate reader (Molecular Devices Corp., Sunnyvale, Calif.), while anti-P. gingivalis IgG levels were read at OD₄₀₅. Marginal bone height measurements were calculated from periapical radiographs as described previously (15). A multivariate repeated measures analysis (MANOVA) was used to compare mean levels between control and immunized monkeys to assess the effect of immunization and to compare mean levels between ligated and nonligated sites to assess the effects of ligation. Data for inflammatory mediators were analyzed on a natural log scale to normalize their distribution. Since the effects of ligation and immunization were similar at both time points, the data from weeks 20 and 36 were combined to decrease variability. If a significant interaction between the immunization effect and ligation effect was present (P < 0.01), separate MANOVAs were also performed for ligated and nonligated sites to assess the effect of immunization. In the same manner, separate analyses were performed to assess the effect of ligation for control and immunized monkeys. For all other comparisons, the significance level was set at P = 0.05. Statistical analysis was performed with SAS software (Cary, N.C.).

The systemic immunization of M. fascicularis with P. gingivalis resulted in an expected significant (P < 0.001) increase in anti-P.gingivalis IgG expression in GCF from nonligated sites (Fig. 1). Immunization had no apparent effect on the ligated sites, since these sites already exhibited relatively high levels of IgG in both immunized and control animals.

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FIG. 1. Effect of immunization on antibody expression. GCF samples collected from both ligated and nonligated sites from immunized and control animals were assayed for the P. gingivalis-specific antibody by ELISA. The data presented are the mean and standard error of triplicate assays. A statistically significant change from control nonligated animals is indicated by ** (P < 0.001).

The effects of immunization on PGE₂ expression were more pronounced in the GCF from ligated sites in control animals (Fig. 2). Ligation caused a 10-fold increase in PGE₂ expression, which was significantly (P < 0.0001) reduced in M. fascicularis monkeys immunized with P. gingivalis. The levels of IL-1ß, TNF-, and PGE₂ were low in control animals in nonligated sites, and the vaccination protocol did not appreciably decrease these already low levels. While IL-1ß levels did not increase in ligated sites after immunization, the expression of TNF- did show a small but significant increase (P < 0.05).

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FIG. 2. Effect of immunization and ligation on mediator expression. GCFs collected from immunized and control animals were assayed for the indicated inflammatory mediators. The data presented are the mean and standard error of triplicate assays. Statistically significant changes from ligated sites in control animals are indicated by * (P < 0.05) and *** (P < 0.0001).

To determine the relationship between the mediator levels and bone height in our study, we plotted the mean PGE₂ present in ligated sites as compared to their bone height measurements (Fig. 3). There was an apparent positive but weak correlation between PGE₂ levels and bone height (r = 0.30, P = 0.027). The graph also illustrates how the majority of the immunized animals reported lower PGE₂ levels and less bone loss than the control monkeys. Levels of the other mediators (IL-1ß, TNF-, and IgG) did not significantly correlate with bone height change (data not shown). A correlation trend (P < 0.07) also existed between PGE₂ levels and computer-assisted densitometric image analysis bone density scores (data not shown).

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FIG. 3. Correlation of PGE2 with bone height. Shown are scatter plot and linear regression analyses of GCF levels of PGE2 compared to radiographic bone height measurements at ligated sites in control and immunized animals (P = 0.027, r = 0.30).

In a previous report, animals immunized with P. gingivalis displayed significant bone loss reduction compared to the control group (15). To investigate the possible mechanism involved in the immunization's protection against ligature-induced periodontitis, we assessed inflammatory mediator levels in the GCF of immunized and control animals at weeks 20 (first visit after ligature placement) and 36 (final visit). We chose to look at IL-1ß, PGE₂, and TNF-, because their expression occurs in periodontitis along with the loss of connective tissue and bone. Although immunization minimally altered IL-1ß and TNF- levels, ligation caused a large increase in PGE₂ in nonimmunized animals that was almost totally blocked by immunization. A weak but significant correlation was found between lower PGE₂ levels in GCF from these sites and reduction in alveolar bone height measurements in the immunized animals (i.e., lower PGE₂ corresponding to less bone loss). Therefore, other factors are also involved with PGE₂ in bone loss.

While we saw slightly higher IL-1ß and TNF- levels in the immunized animals, the crevicular fluid PGE₂ levels were markedly depressed, suggesting an immunization effect may have occurred prior to PGE₂ production. One biological effect of PGE₂ is bone demineralization (16), and therefore decreased PGE₂ production would likely lead to a slower progression of alveolar bone loss and bone height. Although it is unclear why IL-1ß and TNF- levels were not reduced by immunization, decreased PGE₂ production does suggest a possible mechanism for the protective effects of the vaccine. PGE₂ is a major inflammatory mediator stimulated in response to a gram-negative infection (5, 8), and the importance of the levels of PGE₂ in GCF may outweigh that of TNF- and/or IL-1ß. Interestingly, it is becoming clear that prostaglandins have a wider range of effects than previously thought and that localized concentrations found in periodontitis may induce other adverse health effects in the body (1, 2).

Only control animals showed a significant difference in GCF antibody levels between ligated and nonligated teeth. This is most likely due to local inoculation of P. gingivalis or other cross-reactive oral bacteria into the periodontal tissues via ligature placement in the control animals. In the immunized animals, a systemic antibody response was probably already in place, and therefore no significant increase in local antibody titers occurred from the ligature placement.

These animal model results support the association between high PGE₂ levels and increased bone loss in periodontitis. They suggest that immunization may be associated with a decrease in PGE₂ levels and reduced bone loss. Given that PGE₂ is a major component involved in bone demineralization, further investigation into the mechanisms of blocking inflammatory bone loss by immunization is needed.

 
This work was supported by Public Health Service grants DE-12939, DE-00431, and DE-08555 from the National Institute of Dental and Craniofacial Research.

We thank Beth Hacker for assistance with the manuscript.

 
* Corresponding author. Mailing address: University of Washington, Department of Periodontics, Box 357444, Seattle, WA 98195-7444. Phone: (206) 685-9046. Fax: (206) 616-7478. E-mail: froberts{at}u.washington.edu.

Editor: D. L. Burns

Top Abstract Introduction References

 

1
1. Collins, J. G., H. W. Windley III, R. R. Arnold, and S. Offenbacher. 1994. Effects of a Porphyromonas gingivalis infection on inflammatory mediator response and pregnancy outcome in hamsters. Infect. Immun. 62:4356-4361.[Abstract/Free Full Text]
2
2. Deshpande, R. G., M. Khan, and C. A. Genco. 1998. Invasion strategies of the oral pathogen Porphyromonas gingivalis: implications for cardiovascular disease. Invasion Metastasis 18:57-69.[CrossRef][Medline]
3
3. Dinarello, C. A., S. Gatti, and T. Bartfai. 1999. Fever: links with an ancient receptor. Curr. Biol. 9:R147-R150.[CrossRef][Medline]
4
4. Haffajee, A. D., and S. S. Socransky. 1994. Microbial etiological agents of destructive periodontal diseases. Periodontol. 2000 5:78-111.
5
5. Hersh, D., J. Weiss, and A. Zychlinsky. 1998. How bacteria initiate inflammation: aspects of the emerging story. Curr. Opin. Microbiol. 1:43-48.[CrossRef][Medline]
6
6. Houston, L. S., S. A. Lukehart, G. R. Persson, and R. C. Page. 1999. Function of anti-Porphyromonas gingivalis immunoglobulin classes in immunized Macaca fascicularis. Oral Microbiol. Immunol. 14:86-91.[CrossRef][Medline]
7
7. Hussain, M. Z., Q. P. Ghani, J. C. Zhang, B. Enriquez, C. Hayashi, and M. R. Wirthlin. 1994. Alterations of fibroblast metabolism in early ligature-induced periodontitis in the cynomolgus monkey. J. Periodontol. 65:771-775.[Medline]
8
8. Miyauchi, M., N. Ijuhin, H. Nikai, T. Takata, H. Ito, and I. Ogawa. 1992. Effect of exogenously applied prostaglandin E₂ on alveolar bone loss—histometric analysis. J. Periodontol. 63:405-411.[Medline]
9
9. Moore, W. E., and L. V. Moore. 1994. The bacteria of periodontal diseases. Periodontol. 2000 5:66-77.[CrossRef]
10
10. Offenbacher, S., P. A. Heasman, and J. G. Collins. 1993. Modulation of host PGE₂ secretion as a determinant of periodontal disease expression. J. Periodontol. 64:432-444.[Medline]
11
11. Offenbacher, S., B. M. Odle, L. D. Braswell, H. G. Johnson, C. M. Hall, H. McClure, J. L. Orkin, E. A. Strobert, and M. D. Green. 1989. Changes in cyclooxygenase metabolites in experimental periodontitis in Macaca mulatta. J. Periodontal Res. 24:63-74.[CrossRef][Medline]
12
12. Page, R. C. 1991. The role of inflammatory mediators in the pathogenesis of periodontal disease. J. Periodontal Res. 26:230-242.[CrossRef][Medline]
13
13. Page, R. C., and K. S. Kornman. 1997. The pathogenesis of human periodontitis: an introduction. Periodontol. 2000 14:9-11.
14
14. Paludan, S. R. 2000. Synergistic action of pro-inflammatory agents: cellular and molecular aspects. J. Leukoc. Biol. 67:18-25.[Abstract]
15
15. Persson, G. R., D. Engel, C. Whitney, R. Darveau, A. Weinberg, M. Brunsvold, and R. C. Page. 1994. Immunization against Porphyromonas gingivalis inhibits progression of experimental periodontitis in nonhuman primates. Infect. Immun. 62:1026-1031.[Abstract/Free Full Text]
16
16. Raisz, L. G. 1999. Prostaglandins and bone: physiology and pathophysiology. Osteoarthritis Cartilage 7:419-421.[CrossRef][Medline]

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Infection and Immunity, February 2004, p. 1166-1168, Vol. 72, No. 2
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.2.1166-1168.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

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This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Roberts, F. A. Articles by Page, R. C. Search for Related Content PubMed PubMed Citation Articles by Roberts, F. A. Articles by Page, R. C.