Differential human Th22-lymphocyte response triggered by Aggregatibacter actinomycetemcomitans serotypes
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Díaz Zúñiga, Jaime
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Differential human Th22-lymphocyte response triggered by Aggregatibacter actinomycetemcomitans serotypes
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Abstract
Objective: In Aggregatibacter actinomycetemcomitans, different serotypes have been described based on
lipopolysaccharide (LPS) antigenicity. When T lymphocytes were stimulated with these serotypes,
different patterns of T-helper (Th)1 and Th17-type of immune responses were reported. Recently, two
new Th phenotypes have been described and named Th9 and Th22 lymphocytes; however, their role in
the pathogenesis of periodontitis remains unclear. This study aimed to investigate the potential Th9 and/
or Th22 lymphocyte responses when stimulated with autologous dendritic cells infected with different A.
actinomycetemcomitans serotypes.
Methods: Monocyte-derived dendritic cells and naïve CD4+ T lymphocytes were obtained from healthy
donors and stimulated with different serotypes of A. actinomycetemcomitans at a multiplicity of infection
MOI = 102 or their purified LPS (10–50 ng/ml). The levels for the Th9 and Th22-associated cytokines, as
well as the transcription factor master-switch genes implied in their differentiation Spi-B and AhR, were
quantified by qPCR and ELISA.
Results: When stimulated with the serotype b of A. actinomycetemcomitans, higher levels of interleukin
(IL)-6 and tumor necrosis factor (TNF)-a were detected in dendritic cells, as well as higher levels of IL-22
and AhR were detected in T lymphocytes, when compared with stimulation with the other serotypes.
Conclusions: The serotype b of A. actinomycetemcomitans has a higher capacity of trigger Th22-type of
immune response in both dendritic cells and T lymphocytes. These data allow us to suggest that, when
the serotype b of A. actinomycetemcomitans is a significant part of the subgingival biofilm, the Th22
polarization might be triggered within the periodontal lesion.
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URI: https://repositorio.uchile.cl/handle/2250/159184
DOI: 10.1016/j.archoralbio.2017.02.008
ISSN: 18791506
00039969
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Archives of Oral Biology, Volumen 78, 2017, Pages 26-33.
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