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231223s2006 xx ||||| 00| ||eng c |
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|a pubmed24n0546.xml
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|a (DE-627)NLM163721084
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|a (NLM)16797237
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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100 |
1 |
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|a Watanabe, Tomoko
|e verfasserin
|4 aut
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245 |
1 |
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|a CD52 is a novel costimulatory molecule for induction of CD4+ regulatory T cells
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|c 2006
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|a Text
|b txt
|2 rdacontent
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|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
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|a Band
|b nc
|2 rdacarrier
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500 |
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|a Date Completed 26.09.2006
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|a Date Revised 03.01.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a We previously reported that 4C8 monoclonal antibody (mAb) provides a costimulatory signal to human CD4+ T cells and consequently induces regulatory T (Treg) cells, which are hypo-responsive and suppress the polyclonal response of bystander CD4+ cells in a contact-dependent manner. In this study, we identified the antigen of 4C8 mAb as CD52. Costimulation with Campath-1H, a humanized anti-CD52 mAb, also induced Treg cells. Anti-CD52-induced Treg cells suppressed the proliferation of both CD4+ and CD8+ T cells provided with polyclonal or allogeneic stimulation. When Treg cells were induced from Staphylococcal enterotoxin B (SEB) treated cells, they suppressed the response to SEB more efficiently than that to another superantigen, SEA. Furthermore, anti-CD52-induced Treg cells could be expanded by culture with IL-2 followed by CD52-costimulation, and co-injection of expanded Treg cells suppressed lethal xenogeneic graft versus host disease (GvHD) reactions in SCID mice caused by human peripheral blood mononuclear cells (PBMCs)
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|a Journal Article
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|a 4C8 antigen, human
|2 NLM
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650 |
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|a Antibodies, Monoclonal
|2 NLM
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650 |
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|a Antibodies, Monoclonal, Humanized
|2 NLM
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650 |
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|a Antibodies, Neoplasm
|2 NLM
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7 |
|a Antigens, CD
|2 NLM
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|a Antigens, Neoplasm
|2 NLM
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|a CD52 Antigen
|2 NLM
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|a CD52 protein, human
|2 NLM
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|a Enterotoxins
|2 NLM
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7 |
|a Epitopes, T-Lymphocyte
|2 NLM
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650 |
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7 |
|a FOXP3 protein, human
|2 NLM
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|a Forkhead Transcription Factors
|2 NLM
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|a Glycoproteins
|2 NLM
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|a Interleukin-2
|2 NLM
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7 |
|a enterotoxin B, staphylococcal
|2 NLM
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650 |
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7 |
|a 39424-53-8
|2 NLM
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650 |
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7 |
|a Alemtuzumab
|2 NLM
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650 |
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7 |
|a 3A189DH42V
|2 NLM
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700 |
1 |
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|a Masuyama, Jun-ichi
|e verfasserin
|4 aut
|
700 |
1 |
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|a Sohma, Yoshiaki
|e verfasserin
|4 aut
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700 |
1 |
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|a Inazawa, Hiroko
|e verfasserin
|4 aut
|
700 |
1 |
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|a Horie, Kaori
|e verfasserin
|4 aut
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700 |
1 |
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|a Kojima, Kumiko
|e verfasserin
|4 aut
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700 |
1 |
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|a Uemura, Yasunori
|e verfasserin
|4 aut
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700 |
1 |
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|a Aoki, Yumi
|e verfasserin
|4 aut
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700 |
1 |
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|a Kaga, Shuji
|e verfasserin
|4 aut
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700 |
1 |
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|a Minota, Seiji
|e verfasserin
|4 aut
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700 |
1 |
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|a Tanaka, Toshiyuki
|e verfasserin
|4 aut
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700 |
1 |
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|a Yamaguchi, Yasunori
|e verfasserin
|4 aut
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700 |
1 |
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|a Kobayashi, Tetsuto
|e verfasserin
|4 aut
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700 |
1 |
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|a Serizawa, Isao
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 120(2006), 3 vom: 04. Sept., Seite 247-59
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
|
773 |
1 |
8 |
|g volume:120
|g year:2006
|g number:3
|g day:04
|g month:09
|g pages:247-59
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912 |
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|a GBV_USEFLAG_A
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912 |
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|a SYSFLAG_A
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912 |
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|a GBV_NLM
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912 |
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|a GBV_ILN_11
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|a GBV_ILN_24
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912 |
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|a GBV_ILN_350
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951 |
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|a AR
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952 |
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|d 120
|j 2006
|e 3
|b 04
|c 09
|h 247-59
|