Document 0090 DOCN M95B0090 TI Protective immunity to Porphyromonas gingivalis infection in a murine model. DT 9511 AU Bird PS; Gemmell E; Polak B; Paton RG; Sosroseno W; Seymour GJ; Department of Dentistry, University of Queensland, Australia. SO J Periodontol. 1995 May;66(5):351-62. Unique Identifier : AIDSLINE MED/95348944 AB The mouse abscess model has been used extensively to demonstrate protection after challenge with periodontopathic organisms. In the present study, an outer membrane (OM) preparation of P. gingivalis ATCC 33277 was used to immunize BALB/c mice prior to challenge with live P. gingivalis organisms. This OM preparation, particularly at the highest dose level of 100 micrograms/immunization, was able to induce high levels of specific antibody and subsequent protective immunity. Protection in all immunized mice was noted by the rapid healing of the primary lesions, a low incidence of secondary lesions, and, in the highest dose group, an absence of septicemia. Non-immunized animals demonstrated a slower development as well as healing of primary lesions, with higher numbers and larger sizes of secondary lesions. Weight loss and behavior patterns such as hunched bodies, ruffled hair, and stiffness of the hind legs were particularly noted in this group. Depletion of CD4 T cells in mice prior to immunization with 100 micrograms P. gingivalis OM resulted in significantly depressed serum levels of anti-P. gingivalis antibody and an increase in the physical signs of disease compared with both the immunized and control groups. Western blot analysis demonstrated three antigen bands (63.3, 50.1, and 45.1) recognized by all immunized groups and also the control non-immunized group, although the latter recognition occurred only after challenge. A further antigen band of 36.1 kDa was recognized by sera from the highest dose group only. This study has demonstrated the ability of P. gingivalis OM to provide protection against challenge with live P. gingivalis organisms. The increased physical signs of disease seen in the CD4 depleted animals compared with the control group not only illustrate the protective role of serum antibody, but also suggest a possible role for T cell mechanisms in control of the lesion locally. The ability of specific OM antigens to provide similar protective immunity remains to be ascertained. DE Analysis of Variance Animal Antibodies, Bacterial/BIOSYNTHESIS/BLOOD Antigens, Bacterial/ISOLATION & PURIF Bacterial Outer Membrane Proteins/IMMUNOLOGY *Bacterial Vaccines Bacteroidaceae Infections/IMMUNOLOGY/*PREVENTION & CONTROL Blotting, Western CD4 Lymphocyte Count Electrophoresis, Polyacrylamide Gel Enzyme-Linked Immunosorbent Assay Female Male Mice Mice, Inbred BALB C Periodontal Abscess/IMMUNOLOGY/MICROBIOLOGY/*PREVENTION & CONTROL Porphyromonas gingivalis/*IMMUNOLOGY Support, Non-U.S. Gov't Vaccination JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).