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231226s2023 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2023.109737
|2 doi
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|a pubmed25n1202.xml
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|a (DE-627)NLM360858708
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|a (NLM)37586672
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|a (PII)S1521-6616(23)00500-4
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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 Wang, Chuang-Wei
|e verfasserin
|4 aut
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| 245 |
1 |
0 |
|a Clinical characteristics and immune profiles of patients with immune-mediated alopecia associated with COVID-19 vaccinations
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| 264 |
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1 |
|c 2023
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| 336 |
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|a Text
|b txt
|2 rdacontent
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| 337 |
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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 02.10.2023
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| 500 |
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|a Date Revised 02.10.2023
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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| 520 |
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|a Copyright © 2023. Published by Elsevier Inc.
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|a BACKGROUND: The clinical characteristics and pathomechanism for immune-mediated alopecia following COVID-19 vaccinations are not clearly characterized
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| 520 |
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|a OBJECTIVE: We investigated the causality and immune mechanism of COVID-19 vaccines-related alopecia areata (AA)
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| 520 |
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|a STUDY DESIGN: 27 new-onset of AA patients after COVID-19 vaccinations and 106 vaccines-tolerant individuals were enrolled from multiple medical centers for analysis
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| 520 |
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|a RESULTS: The antinuclear antibody, total IgE, granulysin, and PARC/CCL18 as well as peripheral eosinophil count were significantly elevated in the patients with COVID-19 vaccines-related AA compared with those in the tolerant individuals (P = 2.03 × 10-5-0.039). In vitro lymphocyte activation test revealed that granulysin, granzyme B, and IFN-γ released from the T cells of COVID-19 vaccines-related AA patients could be significantly increased by COVID-19 vaccine excipients (polyethylene glycol 2000 and polysorbate 80) or spike protein (P = 0.002-0.04)
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| 520 |
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|a CONCLUSIONS: Spike protein and excipients of COVID-19 vaccines could trigger T cell-mediated cytotoxicity, which contributes to the pathogenesis of immune-mediated alopecia associated with COVID-19 vaccines
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| 650 |
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4 |
|a Journal Article
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| 650 |
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4 |
|a Research Support, Non-U.S. Gov't
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| 650 |
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4 |
|a Alopecia areata
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| 650 |
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4 |
|a Autoimmune disease
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| 650 |
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4 |
|a COVID-19 vaccine
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| 650 |
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4 |
|a Granulysin
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| 650 |
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4 |
|a Lymphocyte activation test
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| 650 |
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4 |
|a Polyethylene glycol
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| 650 |
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4 |
|a Spike protein
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| 650 |
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7 |
|a COVID-19 Vaccines
|2 NLM
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| 650 |
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7 |
|a Spike Glycoprotein, Coronavirus
|2 NLM
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| 650 |
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7 |
|a spike protein, SARS-CoV-2
|2 NLM
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| 700 |
1 |
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|a Wu, Ming-Ying
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Chen, Chun-Bing
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Lin, Wei-Chen
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Wu, Jennifer
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Lu, Chun-Wei
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Chen, Wei-Ti
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Wang, Fang-Ying
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Hui, Rosaline Chung-Yee
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Chi, Min-Hui
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Chiu, Tsu-Man
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Chang, Ya-Ching
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Lin, Jing Yi
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Lin, Yang Yu-Wei
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Tsai, Wan-Ting
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Hung, Shuen-Iu
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Chung, Wen-Hung
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 255(2023) vom: 01. Okt., Seite 109737
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnas
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| 773 |
1 |
8 |
|g volume:255
|g year:2023
|g day:01
|g month:10
|g pages:109737
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| 856 |
4 |
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|u http://dx.doi.org/10.1016/j.clim.2023.109737
|3 Volltext
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|a GBV_USEFLAG_A
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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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| 912 |
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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 255
|j 2023
|b 01
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|h 109737
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