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231223s2009 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2009.05.018
|2 doi
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|a pubmed24n0632.xml
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|a (DE-627)NLM189641843
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|a (NLM)19564135
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Morshed, Sufi R
|e verfasserin
|4 aut
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|a Beta-galactosylceramide alters invariant natural killer T cell function and is effective treatment for lupus
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|c 2009
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 01.09.2009
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|a Date Revised 20.10.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a NZB/W female mice spontaneously develop systemic lupus, an autoantibody mediated disease associated with immune complex glomerulonephritis. Natural killer (NK) T cells augment anti-dsDNA antibody secretion by NZB/W B cells in vitro, and blocking NKT cell activation in vivo with anti-CD1 mAb ameliorates lupus disease activity. In the current study, we show that beta-galactosylceramide reduces the in vivo induction of serum IFN-gamma and/or IL-4 by the potent NKT cell agonist alpha-galactosylceramide and reduces NKT cell helper activity for IgG secretion. Treatment of NZB/W mice with the beta-galactosylceramide ameliorated lupus disease activity as judged by improvement in proteinuria, renal histopathology, IgG anti-dsDNA antibody formation, and survival. In conclusion, beta-galactosylceramide, a glycolipid that reduces the cytokine secretion induced by a potent NKT cell agonist ameliorates lupus in NZB/W mice
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|a Journal Article
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|a Antibodies, Antinuclear
|2 NLM
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|a Antigens, CD1d
|2 NLM
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|a Ceramides
|2 NLM
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|a Monosaccharides
|2 NLM
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|a Receptors, Antigen, T-Cell
|2 NLM
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|a Receptors, Antigen, T-Cell, alpha-beta
|2 NLM
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|a beta-galactosyl ceramide
|2 NLM
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|a Interleukin-4
|2 NLM
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|a 207137-56-2
|2 NLM
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|a Interferon-gamma
|2 NLM
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|a 82115-62-6
|2 NLM
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1 |
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|a Takahashi, Tsuyoshi
|e verfasserin
|4 aut
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1 |
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|a Savage, Paul B
|e verfasserin
|4 aut
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1 |
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|a Kambham, Neeraja
|e verfasserin
|4 aut
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1 |
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|a Strober, Samuel
|e verfasserin
|4 aut
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773 |
0 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 132(2009), 3 vom: 15. Sept., Seite 321-33
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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773 |
1 |
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|g volume:132
|g year:2009
|g number:3
|g day:15
|g month:09
|g pages:321-33
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|u http://dx.doi.org/10.1016/j.clim.2009.05.018
|3 Volltext
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|a AR
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|d 132
|j 2009
|e 3
|b 15
|c 09
|h 321-33
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