Regular ArticleImpaired T Cell Function in RANTES-Deficient Mice
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2020, Molecular ImmunologyCitation Excerpt :RANTES is associated with a Th1 immune response (Culley et al., 2006; Schrum et al., 1996). RANTES-deficient mice show impaired T cell function (Makino et al., 2002). Our ELISA studies with RANTES shows that it drastically decreased in the serum of CN infected group (P < 0.0001) in contrast to the N group (Fig. 1C).
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2018, Dental MaterialsCitation Excerpt :Furthermore, CCL5/RANTES is a member of the CC chemokine family with significant activity toward monocytes and eosinophils [46], shown to be expressed in healthy human pulp [47]. This chemokine is known to upregulate IL-12 [48] and INF-γ [49], both shown here in significantly higher levels after cell treatments in comparison to Ctr group. In Dentistry, the mineral trioxide aggregate was shown to downregulate expression of some cytokines in mouse pulp tissue, including IFN-γ and CCL5/RANTES [50].
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2017, Journal of HepatologyCitation Excerpt :We generated mice carrying the loxP-site-flanked NEMO/IKKγ gene under the control of the Alb/AFP-Cre promotor/enhancer as previously described [15,16,19]. From NEMOΔhepa mice, we generated double knockout animals by crossing NEMOΔhepa with constitutive CCL5 deficient mice defined in a C57BL/6 background and purchased from the Jackson Laboratory (Bar Harbor, ME) [20]. Progression of liver disease was monitored in male mice, ranging from 8 to 52 weeks of age.
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To whom correspondence and reprint requests should be addressed at Department of Molecular Immunology, Chiba University Graduate School of Medicine, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan. Fax: +81-43-227-1498. E-mail: [email protected].