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        <full_title>The Open Dentistry Journal</full_title>
        <abbrev_title>TODENTJ</abbrev_title>
        <issn media_type="print">1874-2106</issn>
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        <publication_date media_type="print">
          <month>09</month>
          <day>30</day>
          <year>2016</year>
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        <journal_volume>
          <volume>10</volume>
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        <issue>1</issue>
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        <titles>
          <title>Promotion of Nickel (Ni) Allergy by Anamnestic Sensitization with a Bacterial Component, Lipopolysaccharide (LPS), in Mice</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first">
            <given_name>Norimasa</given_name>
            <surname>Adachi</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Eiji</given_name>
            <surname>Takayama</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Makoto</given_name>
            <surname>Adachi</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Masako</given_name>
            <surname>Mizuno-Kamiya</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Harumi</given_name>
            <surname>Kawaki</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Hiroko</given_name>
            <surname>Takeuchi</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Shuri</given_name>
            <surname>Kubo</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Hajime</given_name>
            <surname>Ishigami</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Masakazu</given_name>
            <surname>Kurachi</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>Nobuo</given_name>
            <surname>Kondoh</surname>
          </person_name>
        </contributors>
        <jats:abstract>
                <jats:sec>
                    <jats:title>Background/Objective:</jats:title>
                    <jats:p>Lipopolysaccharides (LPS) promote allergic responses to nickel (Ni) both in the sensitization and elicitation steps. In this study, we examine the effect of pre-sensitization to LPS on the occurrence of Ni allergy using a mouse model.</jats:p>
                </jats:sec>
                <jats:sec>
                    <jats:title>Method:</jats:title>
                    <jats:p>A 100 mg of LPS was injected into C57BL/6J mice intraperitoneally (ip). Three weeks later, the mice were subsequently injected with 0.3 μ moles of nickel dichloride (NiCl<jats:sub>2</jats:sub>) and 100 μg of CpG-DNA, which acted as an adjuvant. The mice were repeatedly immunized with the 0.3 μg of nickel sulfate (NiSO<jats:sub>4</jats:sub>), along with 300 μl of the adjuvant, Inject Alum (Pierce, USA). Then we examined the producing capabilities of T helper type 1 (Th1) and 2 (Th2) cytokines (interferon-gamma- (IFN)-γ and interleukin (IL)-10, respectively) from anti CD3 antibody-stimulated spleen cells.</jats:p>
                </jats:sec>
                <jats:sec>
                    <jats:title>Results:</jats:title>
                    <jats:p>Pre-treatment with LPS, followed by repeated challenges with Ni<jats:sup>2+</jats:sup> and adjuvants significantly enhanced the IFN-γ-producing capability of spleen cells (n=5, p&lt;0.01); however, that could not enhance the capability of spleen cells by a single challenge with Ni<jats:sup>2+</jats:sup> and adjuvants (n=5). In contrast, without LPS treatment, single or even repeated challenges by Ni<jats:sup>2+</jats:sup> could not enhance the IFN-γ-producing capability. On the other hand, the IL-10-producing capability of spleen cells was not enhanced even by LPS and repeated challenges with Ni<jats:sup>2+</jats:sup> and adjuvants.</jats:p>
                </jats:sec>
                <jats:sec>
                    <jats:title>Conclusion:</jats:title>
                    <jats:p>The solitary pre-sensitization to LPS is essential for the onset of Ni allergy by shifting the Th1/Th2 immune balance toward a Th1 dominant.</jats:p>
                </jats:sec>
            </jats:abstract>
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          <month>09</month>
          <day>30</day>
          <year>2016</year>
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          <first_page>531</first_page>
          <last_page>537</last_page>
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