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A Novel Glycolipid Antigen for NKT Cells That Preferentially Induces IFN-γ Production.
Birkholz, Alysia M; Girardi, Enrico; Wingender, Gerhard; Khurana, Archana; Wang, Jing; Zhao, Meng; Zahner, Sonja; Illarionov, Petr A; Wen, Xiangshu; Li, Michelle; Yuan, Weiming; Porcelli, Steven A; Besra, Gurdyal S; Zajonc, Dirk M; Kronenberg, Mitchell.
Afiliación
  • Birkholz AM; Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037; Division of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037; Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92037;
  • Girardi E; Division of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
  • Wingender G; Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
  • Khurana A; Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
  • Wang J; Division of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
  • Zhao M; Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
  • Zahner S; Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
  • Illarionov PA; School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
  • Wen X; Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033;
  • Li M; Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033;
  • Yuan W; Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033;
  • Porcelli SA; Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461; and Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461.
  • Besra GS; School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
  • Zajonc DM; Division of Cell Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
  • Kronenberg M; Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037; Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92037; mitch@liai.org.
J Immunol ; 195(3): 924-33, 2015 Aug 01.
Article en En | MEDLINE | ID: mdl-26078271
In this article, we characterize a novel Ag for invariant NKT (iNKT) cells capable of producing an especially robust Th1 response. This glycosphingolipid, DB06-1, is similar in chemical structure to the well-studied α-galactosylceramide (αGalCer), with the only change being a single atom: the substitution of a carbonyl oxygen with a sulfur atom. Although DB06-1 is not a more effective Ag in vitro, the small chemical change has a marked impact on the ability of this lipid Ag to stimulate iNKT cells in vivo, with increased IFN-γ production at 24 h compared with αGalCer, increased IL-12, and increased activation of NK cells to produce IFN-γ. These changes are correlated with an enhanced ability of DB06-1 to load in the CD1d molecules expressed by dendritic cells in vivo. Moreover, structural studies suggest a tighter fit into the CD1d binding groove by DB06-1 compared with αGalCer. Surprisingly, when iNKT cells previously exposed to DB06-1 are restimulated weeks later, they have greatly increased IL-10 production. Therefore, our data are consistent with a model whereby augmented and or prolonged presentation of a glycolipid Ag leads to increased activation of NK cells and a Th1-skewed immune response, which may result, in part, from enhanced loading into CD1d. Furthermore, our data suggest that strong antigenic stimulation in vivo may lead to the expansion of IL-10-producing iNKT cells, which could counteract the benefits of increased early IFN-γ production.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glicoesfingolípidos / Activación de Linfocitos / Interferón gamma / Células TH1 / Células T Asesinas Naturales / Galactosilceramidas Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glicoesfingolípidos / Activación de Linfocitos / Interferón gamma / Células TH1 / Células T Asesinas Naturales / Galactosilceramidas Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Immunol Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos