PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 18671950-1 2008 The glycolipid alpha-galactosylceramide (alpha-GalCer), when presented on CD1 molecules by antigen presenting cells (APCs) to invariant NKT (iNKT cells), is a potent immunomodulator. alpha-galactosylceramide 15-39 CD1c molecule Homo sapiens 74-77 21575695-2 2012 The high-affinity CD1d antigen alpha-galactosylceramide analogue KRN7000 (KRN) activates a cascade of anti-tumor effector cells and clinical studies have already had some initial success. alpha-galactosylceramide 31-55 CD1c molecule Homo sapiens 18-21 23885215-4 2013 We demonstrate here that CD1c, which is co-expressed with CD1d on blood dendritic cells and on a fraction of B cells, is able to present alpha-galactosylceramide (alpha-GalCer) as a weak agonist to human iNKT cells, and that the presence of CD1c synergistically enhances alpha-GalCerdependent activation of iNKT cells by CD1d. alpha-galactosylceramide 137-161 CD1c molecule Homo sapiens 25-29 23885215-4 2013 We demonstrate here that CD1c, which is co-expressed with CD1d on blood dendritic cells and on a fraction of B cells, is able to present alpha-galactosylceramide (alpha-GalCer) as a weak agonist to human iNKT cells, and that the presence of CD1c synergistically enhances alpha-GalCerdependent activation of iNKT cells by CD1d. alpha-galactosylceramide 137-161 CD1c molecule Homo sapiens 241-245 18671950-1 2008 The glycolipid alpha-galactosylceramide (alpha-GalCer), when presented on CD1 molecules by antigen presenting cells (APCs) to invariant NKT (iNKT cells), is a potent immunomodulator. alpha-galactosylceramide 41-53 CD1c molecule Homo sapiens 74-77 18006319-3 2008 Among the several (glyco)lipids identified to cause T-cell stimulation in complex with CD1, alpha-galactosyl ceramide (alpha-GalCer) is one of the most well studied. alpha-galactosylceramide 92-117 CD1c molecule Homo sapiens 87-90 12360465-3 2002 METHODS: We used a human CD1d (hCD1d) tetramer produced by a baculovirus expressing recombinant CD1d protein complexed with alpha-galactosylceramide (alpha-GalCer) and quantitated hCD1d tetramer reactive cells in blood and liver from controls and patients with primary biliary cirrhosis (PBC). alpha-galactosylceramide 124-148 CD1c molecule Homo sapiens 31-35 17071611-6 2006 Nor were any required for the CD1d molecule to bind and present alpha-galactosyl ceramide after lysosomal processing of a precursor lipid, galactosyl-(alpha1-2)-galactosyl ceramide. alpha-galactosylceramide 64-89 CD1c molecule Homo sapiens 30-33 12076157-1 2002 Alpha-galactosyl ceramide has been identified to be a potent stimulatory agent for a novel immunological process, mediated by CD1 molecules. alpha-galactosylceramide 0-25 CD1c molecule Homo sapiens 126-129 26107189-0 2015 Influence of Endosomal Escape and Degradation of alpha-Galactosylceramide Loaded Liposomes on CD1d Antigen Presentation. alpha-galactosylceramide 49-73 CD1c molecule Homo sapiens 94-97 28104514-3 2017 We have developed an approach of in vivo expansion of Tregs with RGI-2001, a novel liposomal formulation of a synthetic derivative of alpha-galactosylceramide, a naturally occurring ligand that binds to CD1 and activates and expands invariant natural killer cells. alpha-galactosylceramide 134-158 CD1c molecule Homo sapiens 203-206 11970881-2 2002 Classical NKT cells display TCRs of restricted heterogeneity (Valpha14-Jalpha281) and recognize lipid antigens (e.g., alpha-galactosyl ceramide) presented by nonpolymorphic CD1 molecules. alpha-galactosylceramide 118-143 CD1c molecule Homo sapiens 173-176 9782129-4 1998 Mouse or human CD1 molecules can present the glycolipid alpha-galactosylceramide (alpha-GalCer) to NK T cells from either species. alpha-galactosylceramide 56-80 CD1c molecule Homo sapiens 15-18 9782129-4 1998 Mouse or human CD1 molecules can present the glycolipid alpha-galactosylceramide (alpha-GalCer) to NK T cells from either species. alpha-galactosylceramide 82-94 CD1c molecule Homo sapiens 15-18 25248321-8 2015 Furthermore, RA and/or CD38 ligation increased splenocyte proliferation and differentiation after treatment with the CD1 ligand alpha-galactosylceramide (alphaGalCer), evidenced by an increase in the number of splenic dendritic cells, NKT cells, and germinal center plasmacytes. alpha-galactosylceramide 128-152 CD1c molecule Homo sapiens 117-120