» Articles » PMID: 18426881

Nasal Immunization with Porphyromonas Gingivalis Outer Membrane Protein Decreases P. Gingivalis-induced Atherosclerosis and Inflammation in Spontaneously Hyperlipidemic Mice

Overview
Journal Infect Immun
Date 2008 Apr 23
PMID 18426881
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Porphyromonas gingivalis has been shown to accelerate atherosclerotic lesion development in hyperlipidemic animals. We assessed the potential of a nasal vaccine against P. gingivalis infection for the prevention of atherosclerosis. Apolipoprotein E-deficient spontaneously hyperlipidemic (Apoe(shl)) mice were nasally immunized with the 40-kDa outer membrane protein (OMP) of P. gingivalis plus cholera toxin (CT) as adjuvant and then challenged intravenously with P. gingivalis strain 381. The animals were euthanized 11 or 14 weeks later. Atheromatous lesions in the proximal aorta of each animal were analyzed histomorphometrically, and the serum concentrations of 40-kDa OMP-specific antibodies and cytokines were determined. The areas of the aortic sinus that were covered with atherosclerotic plaque and the serum levels of inflammatory cytokines and chemokines were increased in Apoe(shl) mice challenged with P. gingivalis compared to nonchallenged mice. In comparison, nasal immunization with 40-kDa OMP plus CT significantly reduced atherosclerotic plaque accumulation in the aortic sinus and lowered the serum levels of cytokines and chemokines compared to nonimmunized animals. Nasal immunization also induced 40-kDa OMP-specific serum immunoglobulin G (IgG) and saliva IgA antibody responses. These findings suggest that systemic infection with P. gingivalis accelerates atherosclerosis in Apoe(shl) mice, and 40-kDa OMP plus CT may be an effective nasal vaccine for the reduction of atherosclerosis accelerated by P. gingivalis in the hyperlipidemic mouse model.

Citing Articles

Targeting gut microbiota to regulate the adaptive immune response in atherosclerosis.

Giakomidi D, Ishola A, Nus M Front Cardiovasc Med. 2025; 12:1502124.

PMID: 39957996 PMC: 11825770. DOI: 10.3389/fcvm.2025.1502124.


Vaccine: Antigens and Mucosal Adjuvants.

Wang S, Yan T, Zhang B, Chen Y, Li Z Vaccines (Basel). 2024; 12(6).

PMID: 38932348 PMC: 11209493. DOI: 10.3390/vaccines12060619.


Two decades of vaccine development against atherosclerosis.

Moreno-Gonzalez M, Ortega-Rivera O, Steinmetz N Nano Today. 2023; 50.

PMID: 37860053 PMC: 10586238. DOI: 10.1016/j.nantod.2023.101822.


The Roles of Periodontal Bacteria in Atherosclerosis.

Huang X, Xie M, Lu X, Mei F, Song W, Liu Y Int J Mol Sci. 2023; 24(16).

PMID: 37629042 PMC: 10454115. DOI: 10.3390/ijms241612861.


Association between and systemic diseases: Focus on T cells-mediated adaptive immunity.

Li C, Yu R, Ding Y Front Cell Infect Microbiol. 2022; 12:1026457.

PMID: 36467726 PMC: 9712990. DOI: 10.3389/fcimb.2022.1026457.


References
1.
von der Thusen J, Kuiper J, Van Berkel T, Biessen E . Interleukins in atherosclerosis: molecular pathways and therapeutic potential. Pharmacol Rev. 2003; 55(1):133-66. DOI: 10.1124/pr.55.1.5. View

2.
Libby P . Coronary artery injury and the biology of atherosclerosis: inflammation, thrombosis, and stabilization. Am J Cardiol. 2000; 86(8B):3J-8J; discussion 8J-9J. DOI: 10.1016/s0002-9149(00)01339-4. View

3.
Ridker P . On evolutionary biology, inflammation, infection, and the causes of atherosclerosis. Circulation. 2002; 105(1):2-4. View

4.
Koizumi Y, Kurita-Ochiai T, Yamamoto M . Transcutaneous immunization with an outer membrane protein of Porphyromonas gingivalis without adjuvant elicits marked antibody responses. Oral Microbiol Immunol. 2008; 23(2):131-8. DOI: 10.1111/j.1399-302X.2007.00400.x. View

5.
Matsushima Y, Hayashi S, Tachibana M . Spontaneously hyperlipidemic (SHL) mice: Japanese wild mice with apolipoprotein E deficiency. Mamm Genome. 1999; 10(4):352-7. DOI: 10.1007/s003359901000. View