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NLM323317146 |
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DE-627 |
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20250301073900.0 |
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cr uuu---uuuuu |
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231225s2021 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2021.108717
|2 doi
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|a pubmed25n1077.xml
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|a (DE-627)NLM323317146
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|a (NLM)33775870
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|a (PII)S1521-6616(21)00054-1
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|a DE-627
|b ger
|c DE-627
|e rakwb
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| 041 |
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|a eng
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| 100 |
1 |
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|a Yang, Ming
|e verfasserin
|4 aut
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| 245 |
1 |
3 |
|a An Enhanced Expression Level of CXCR3 on Tfh-like Cells from Lupus Skin Lesions Rather Than Lupus Peripheral Blood
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| 264 |
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1 |
|c 2021
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| 336 |
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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| 338 |
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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| 500 |
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|a Date Completed 24.06.2021
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|a Date Revised 24.06.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2021 Elsevier Inc. All rights reserved.
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|a Systemic lupus erythematosus (SLE) is a systemic autoimmune disease, and the etiopathogenesis is unclear. Follicular helper T (Tfh) cells have been reported as an important pathogenic cell type in SLE. CXCR3 was reported to be decreased on lupus peripheral CD4+T cells. However, the expression level of CCR4, CCR6 and CXCR3 on Tfh-like cells in SLE peripheral blood and skin lesions is unknown. In this study, we detected CCR4, CCR6 and CXCR3 expression level on Tfh-like cells in the peripheral blood and skin lesions from SLE patients and normal controls (NCs). A decreased expression level of CXCR3 on Tfh-like cells was found in lupus peripheral blood. However, an increased CXCR3 expression was observed on total CD4+T and Tfh-like cells from lupus skin lesions. Moreover, we observed a higher expression level of CXCR3 in Tfh cells from human tonsils. These findings indicate that CXCR3 might help Tfh-like cells to migrate into the inflammatory sites
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4 |
|a Journal Article
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4 |
|a Research Support, Non-U.S. Gov't
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| 650 |
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4 |
|a CCR4
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| 650 |
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4 |
|a CCR6
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| 650 |
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4 |
|a CXCR3
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| 650 |
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4 |
|a SLE
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| 650 |
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4 |
|a Tfh
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| 650 |
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7 |
|a CXCR3 protein, human
|2 NLM
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| 650 |
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7 |
|a Receptors, CCR4
|2 NLM
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| 650 |
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7 |
|a Receptors, CCR6
|2 NLM
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| 650 |
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7 |
|a Receptors, CXCR3
|2 NLM
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| 700 |
1 |
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|a Cao, Pengpeng
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Zhao, Zhidan
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Wang, Zheyu
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Jia, Chen
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Guo, Yunkai
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Yin, Heng
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Zhao, Ming
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Ding, Yan
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Wu, Haijing
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Lu, Qianjin
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 226(2021) vom: 01. Mai, Seite 108717
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnas
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| 773 |
1 |
8 |
|g volume:226
|g year:2021
|g day:01
|g month:05
|g pages:108717
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| 856 |
4 |
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|u http://dx.doi.org/10.1016/j.clim.2021.108717
|3 Volltext
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|a GBV_USEFLAG_A
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|a SYSFLAG_A
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|a GBV_NLM
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|a GBV_ILN_11
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| 912 |
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|a GBV_ILN_24
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|a GBV_ILN_350
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|a AR
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| 952 |
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|d 226
|j 2021
|b 01
|c 05
|h 108717
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