Literature DB >> 24256118

Serotype-dependent response of human dendritic cells stimulated with Aggregatibacter actinomycetemcomitans.

Jaime Díaz-Zúñiga1, Juan Pablo Yáñez, Carla Alvarez, Samanta Melgar-Rodríguez, Marcela Hernández, Mariano Sanz, Rolando Vernal.   

Abstract

AIM: Different serotypes of Aggregatibacter actinomycetemcomitans have been described based on the lipopolysaccharide (LPS)-O-polysaccharide antigenicity. In turn, a distinct effect of A. actinomycetemcomitans serotypes has been described on cell proliferation and pro-inflammatory cytokine production in different human cells. This study was aimed to investigate the differential dendritic cell (DC) response when stimulated with different bacterial strains belonging to the most prevalent serotypes of A. actinomycetemcomitans (a-c).
MATERIALS AND METHODS: Dendritic cells were obtained from healthy subjects and stimulated with increasing multiplicity of infection (MOI = 10(-1) -10(2)) of A. actinomycetemcomitans, serotypes a-c, or their lipopolysaccharide (10-50 ng/ml). The levels for interferon (IFN)-γ, tumour necrosis factor (TNF)-α, interleukin (IL)-1β, IL-5, IL-6, IL-10, IL-12 and IL-23 were quantified by real-time RT-PCR and ELISA.
RESULTS: Variable DC responses were detected when stimulated with the different strains of A. actinomycetemcomitans. DCs stimulated with A. actinomycetemcomitans strains belonging to the serotype b or their purified LPS expressed higher levels of IL-1β, IL-6, IL-12, IL-23, IFN-γ and TNF-α than DCs stimulated with the other serotypes.
CONCLUSIONS: Aggregatibacter actinomycetemcomitans strains belonging to the serotype b demonstrated a higher capacity to trigger Th1 and Th17-type cytokine production on DCs. These increased potential is likely explained by a higher immunogenicity of their LPS.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Aggregatibacter actinomycetemcomitans; LPS; cytokines; dendritic cells; lipopolysaccharide; serotypes

Mesh:

Substances:

Year:  2013        PMID: 24256118     DOI: 10.1111/jcpe.12205

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


  11 in total

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