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|a 10.1016/j.clim.2023.109843
|2 doi
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|a pubmed24n1371.xml
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|a (PII)S1521-6616(23)00607-1
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|a DE-627
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|a eng
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|a Wang, WenHao
|e verfasserin
|4 aut
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|a Human monoclonal antibodies against Staphylococcus aureus A protein identified by high-throughput single-cell sequencing of phase I clinical volunteers' B cells
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|c 2023
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|a Text
|b txt
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
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|a Date Completed 07.02.2024
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|a Date Revised 10.04.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2023 Elsevier Inc. All rights reserved.
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|a Methicillin-resistant Staphylococcus aureus, poses a significant threat through infections in both community and hospital settings. To address this challenge, we conducted a phase I clinical trial study involving a recombinant Staphylococcus aureus vaccine. Utilizing peripheral blood lymphocytes from 64 subjects, we isolated antigen-specific memory B cells for subsequent single-cell sequencing. Among the 676 identified antigen-binding IgG1+ clones, we selected the top 10 antibody strains for construction within expression vectors. Successful expression and purification of these monoclonal antibodies led to the discovery of a highly expressed human antibody, designated as IgG-6. This antibody specifically targets the pentameric form of the Staphylococcus aureus protein A (SpA5). In vivo assessments revealed that IgG-6 provided prophylactic protection against MRSA252 infection. This study underscores the potential of human antibodies as an innovative strategy against Staphylococcus aureus infections, offering a promising avenue for further research and clinical development
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|a Clinical Trial, Phase I
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Human monoclonal antibody
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|a Single-Cell Sequencing
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|a Staphylococcus aureus
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|a Staphylococcus aureus protein a
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|a Antibodies, Bacterial
|2 NLM
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|a Antibodies, Monoclonal
|2 NLM
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|a Immunoglobulin G
|2 NLM
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700 |
1 |
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|a Gu, YaRu
|e verfasserin
|4 aut
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1 |
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|a Ou, YangXue
|e verfasserin
|4 aut
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700 |
1 |
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|a Zhou, JinRui
|e verfasserin
|4 aut
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700 |
1 |
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|a Liu, BiXia
|e verfasserin
|4 aut
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700 |
1 |
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|a Zuo, HouYi
|e verfasserin
|4 aut
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1 |
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|a Du, YeXiang
|e verfasserin
|4 aut
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1 |
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|a Wang, Ying
|e verfasserin
|4 aut
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700 |
1 |
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|a Tang, TengQian
|e verfasserin
|4 aut
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700 |
1 |
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|a Zou, QuanMing
|e verfasserin
|4 aut
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700 |
1 |
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|a Zuo, QianFei
|e verfasserin
|4 aut
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773 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 257(2023) vom: 01. Dez., Seite 109843
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:257
|g year:2023
|g day:01
|g month:12
|g pages:109843
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|u http://dx.doi.org/10.1016/j.clim.2023.109843
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