Antigenic Complex for the Diagnosis and Treatment of Porphyromonas Gingivalis Infection
an antigen complex and porphyromonas gingivalis technology, applied in the field of multimeric protein complexes, can solve the problems of major public health problems and achieve the effect of high arginine and/or lysine proteolytic activity
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example 1
(1) Preparation of Antigenic Complex
A. Triton X-114 Extraction and Affinity Chromatography.
[0069]Porphyromonas gingivalis was grown in an anaerobic chamber (MK3 anaerobic workstation; Don Whitley Scientific Ltd., Shipley, England) at 37° C. on horse blood agar plates supplemented with 10% (v / v) lysed horse blood. Bacterial colonies were used to inoculate brain heart infusion media containing 5 μg / ml of hemin and 0.5 μg / ml of cysteine for batch culture growth. Batch culture growth was monitored at 650 nm using a spectrophotometer (Perkin-Elmer model 295E). Culture purity was routinely checked by Gram stain, microscopic examination and using a variety of biochemical tests. Stocks were maintained as lyophilised cultures. P. gingivalis cells (2L) were grown to late exponential phase and harvested by centrifugation (7500 g, 30 min, 4° C.) and washed twice with PG buffer (50 mM Tris-HCl, 150 mM NaCl, 5 mM CaCl2, and 5 mM cysteine-HCl, pH 8.0) in the anaerobic workstation. Cells were resus...
example 2
Methods and Compounds for Vaccine Formulations Related to Antigenic Complex
[0076]This embodiment of the present invention is to provide complex protein to be used in as an immunogen in a prophylactic and / or therapeutic vaccine for active immunisation to protect against or treat infections caused by P. gingivalis. For vaccine purposes, an antigen of P. gingivalis comprising a bacterial protein should be immunogenic, and induce functional antibodies directed to one or more surface-exposed epitopes on intact bacteria, wherein the epitope(s) are conserved amongst strains of P. gingivalis.
Protective Efficacy of Immunisation with the Antigenic Complex in Animal Models
[0077]The protective efficacy of the antigenic complex was evaluated in two internationally accepted animal models of P. gingivalis-infection i.e the lesion model and the periodontitis model. For the lesion model of disease, the maximum sizes of the lesions developed were statistically analyzed using the Kruskal-Wallis test ...
example 3
[0083]In one illustration of the antigenic complex having the properties desirable of a vaccine antigen, the protein was purified from P. gingivalis using the method described herein in Example 1. Mice were immunized with the purified inactivated Triton X114 and sonication extracted complex (25 μg) with adjuvant (IFA) two times at four week intervals. The purified complex was inactivated by air oxidation. Blood from the immunized mice was drawn 32 days after the last immunization and the immune sera were pooled. The pooled immune sera were assayed against the complex by an enzyme linked immunosorbent assay (ELISA) and a Western blot. ELISAs were performed in triplicate in wells of flat-bottom polyvinyl microtitre plates (Dynatech laboratories, McLean, Va.) coated with 10 μg / ml of P. gingivalis whole cells in 0.1 M phosphate-buffered saline (PBS), pH 7.4, overnight at 4° C. After removal of coating solution, 2% (w / v) skim milk powder in PBS, pH 7.4, containing 0.1% (v / v) Tween 20 was...
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