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    <dc:date>2013-05-25T18:55:30Z</dc:date>
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    <title>Effect of sialic acid loss on dendritic cell maturation.</title>
    <link>http://hdl.handle.net/10362/7130</link>
    <description>Title: Effect of sialic acid loss on dendritic cell maturation.
Authors: Crespo, HJ; Cabral, MG; Teixeira, AV; Lau, JT; Trindade, H; Videira, PA
Abstract: Sialic acids are key structural determinants and contribute to the functionality
of a number of immune cell receptors. Previously, we demonstrated that
differentiation of human dendritic cells (DCs) is accompanied by an increased
expression of sialylated cell surface structures, putatively through the
activity of the ST3Gal.I and ST6Gal.I sialyltransferases. Furthermore, DC
endocytosis was reduced upon removal of the cell surface sialic acid residues by
neuraminidase. In the present work, we evaluate the contribution of the sialic
acid modifications in DC maturation. We demonstrate that neuraminidase-treated
human DCs have increased expression of major histocompatibility complex (MHC)
and costimulatory molecules, increased gene expression of specific cytokines and
induce a higher proliferative response of T lymphocytes. Together, the data
suggest that clearance of cell surface sialic acids contributes to the
development of a T helper type 1 proinflammatory response. This postulate is
supported by mouse models, where elevated MHC class II and increased maturation
of specific DC subsets were observed in DCs harvested from ST3Gal.I(-/-) and
ST6Gal.I(-/-) mice. Moreover, important qualitative differences, particularly in
the extent of reduced endocytosis and in the peripheral distribution of DC
subsets, existed between the ST3Gal.I(-/-) and ST6Gal.I(-/-) strains. Together,
the data strongly suggest not only a role of cell surface sialic acid
modifications in maturation and functionality of DCs, but also that the sialic
acid linkages created by different sialyltransferases are functionally distinct.
Consequently, with particular relevance to DC-based therapies, cell surface
sialylation, mediated by individual sialyltransferases, can influence the
immunogenicity of DCs upon antigen loading.</description>
    <dc:date>2009-01-01T00:00:00Z</dc:date>
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