Literature DB >> 25070874

IgG sera levels against a subset of periodontopathogens and severity of disease in aggressive periodontitis patients: a cross-sectional study of selected pocket sites.

Luciana Saraiva1, Estela S Rebeis, Eder de S Martins, Ricardo T Sekiguchi, Ellen S Ando-Suguimoto, Carlos Eduardo S Mafra, Marinella Holzhausen, Giuseppe A Romito, Marcia P A Mayer.   

Abstract

AIMS: To evaluate the association among serum immunoglobulin G (IgG) responses to Aggregatibacter actinomycetemcomitans (Aa) serotypes a, b and c, Porphyromonas gingivalis (Pg), Tannerella forsythia (Tf) and clinical parameters in Aggressive Periodontitis (AP) subjects. Associations between periodontal pathogens and clinical and immunological parameters were also evaluated.
METHODS: Thirty-eight subjects diagnosed with generalized AP (GAP) and localized AP (LAP) were included. Ten healthy controls were also evaluated. Clinical parameters were assessed and percentages of subgingival levels of Aa, Pg and Tf (beyond bacterial load), were determined by quantitative real-time polymerase chain reaction. Serum IgG antibody levels against Aa, Pg and Tf were evaluated by enzyme-linked immunosorbent assay.
RESULTS: Percentages of Aa, Pg and Tf were significantly higher in AP than in controls. The response to Aa serotype c was higher in LAP subjects than in controls. There were no differences in microbial composition or antibodies responses between GAP and LAP, except for IgG response to Tf. Pg levels were correlated with probing depth (PD), BoP and CAL in GAP but not in LAP subjects. Tf levels correlated with PD and CAL in GAP subjects. In GAP, the infection levels of Aa and Pg correlated with the corresponding IgG levels to Aa serotype c and Pg.
CONCLUSION: Given the evidences that IgG response in AP patients correlated with bacterial infection level in GAP, but not in LAP, and that LAP patients lack a response to Tf, despite harbouring this species, our data suggest a difference in host immune defence between these two forms of aggressive periodontitis.
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Aggregatibacter actinomycetemcomitans; Porphyromonas gingivalis; Tannerella forsythia; aggressive periodontitis; antibodies; qPCR

Mesh:

Substances:

Year:  2014        PMID: 25070874     DOI: 10.1111/jcpe.12296

Source DB:  PubMed          Journal:  J Clin Periodontol        ISSN: 0303-6979            Impact factor:   8.728


  6 in total

1.  Integrated biomarker profiling of smokers with periodontitis.

Authors:  Radhakrishnan Nagarajan; Mohanad Al-Sabbagh; Dolph Dawson; Jeffrey L Ebersole
Journal:  J Clin Periodontol       Date:  2017-02-02       Impact factor: 8.728

Review 2.  Polymorphisms in Genes Involved in Inflammation and Periodontitis: A Narrative Review.

Authors:  Aniela Brodzikowska; Bartłomiej Górski
Journal:  Biomolecules       Date:  2022-04-07

3.  Ageing effects on humoral immune responses in chronic periodontitis.

Authors:  Jeffrey L Ebersole; Mohanad Al-Sabbagh; Octavio A Gonzalez; Dolph R Dawson
Journal:  J Clin Periodontol       Date:  2018-04-26       Impact factor: 8.728

4.  Age and Periodontal Health - Immunological View.

Authors:  J L Ebersole; D A Dawson; P Emecen Huja; S Pandruvada; A Basu; L Nguyen; Y Zhang; O A Gonzalez
Journal:  Curr Oral Health Rep       Date:  2018-11-07

Review 5.  Mechanisms Involved in the Association between Periodontitis and Complications in Pregnancy.

Authors:  Marcela Yang Hui Zi; Priscila Larcher Longo; Bruno Bueno-Silva; Marcia Pinto Alves Mayer
Journal:  Front Public Health       Date:  2015-01-29

6.  Epigenetic regulation of inflammation in localized aggressive periodontitis.

Authors:  L M Shaddox; A F Mullersman; H Huang; S M Wallet; T Langaee; I Aukhil
Journal:  Clin Epigenetics       Date:  2017-09-02       Impact factor: 6.551

  6 in total

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