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231223s2010 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2010.02.016
|2 doi
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|a pubmed24n0657.xml
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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 Arai, Takashi
|e verfasserin
|4 aut
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|a Administration of a determinant of preproinsulin can induce regulatory T cells and suppress anti-islet autoimmunity in NOD mice
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|c 2010
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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 06.08.2010
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|a Date Revised 17.11.2011
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a (c) 2010 Elsevier Inc. All rights reserved.
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|a Antigen-specific immunotherapy is expected to be an ideal strategy for treating type 1 diabetes (T1D). We investigated the therapeutic efficacy of a peptide in the leader sequence of preproinsulin, which was selected because of its binding affinity to the MHC I-A(g7) molecule. Preproinsulin-1 L7-24 peptide (L7-24) emulsified in Freund's incomplete adjuvant was administered subcutaneously to NOD mice. Administration of L7-24 increased the proportion of regulatory T cells in the spleen. Splenocytes of NOD mice immunized with this peptide secreted IL-4 and IL-10 in response to L7-24. This peptide also significantly prevented the development of diabetes and cured some newly diabetic NOD mice without recurrence. L7-24 peptide, which has a high affinity for pockets of I-A(g7), induced regulatory T cells and showed therapeutic effects. This peptide may provide a new approach for developing antigen-specific immunotherapy for autoimmune diabetes
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|a Journal Article
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|a Blood Glucose
|2 NLM
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|a Forkhead Transcription Factors
|2 NLM
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|a Foxp3 protein, mouse
|2 NLM
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|a Histocompatibility Antigens Class II
|2 NLM
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|a Insulin
|2 NLM
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|a Peptide Fragments
|2 NLM
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|a Protein Precursors
|2 NLM
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|a Transforming Growth Factor beta
|2 NLM
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|a Concanavalin A
|2 NLM
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|a 11028-71-0
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|a Interleukin-10
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|a 130068-27-8
|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 preproinsulin
|2 NLM
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|a 61116-24-3
|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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|a Moriyama, Hiroaki
|e verfasserin
|4 aut
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|a Shimizu, Mami
|e verfasserin
|4 aut
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|a Sasaki, Hirotomo
|e verfasserin
|4 aut
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|a Kishi, Minoru
|e verfasserin
|4 aut
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|a Okumachi, Yasuyo
|e verfasserin
|4 aut
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|a Yasuda, Hisafumi
|e verfasserin
|4 aut
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|a Hara, Kenta
|e verfasserin
|4 aut
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|a Yokono, Koichi
|e verfasserin
|4 aut
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|a Nagata, Masao
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 136(2010), 1 vom: 03. Juli, Seite 74-82
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:136
|g year:2010
|g number:1
|g day:03
|g month:07
|g pages:74-82
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|u http://dx.doi.org/10.1016/j.clim.2010.02.016
|3 Volltext
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|d 136
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