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排序方式: 共有10000条查询结果,搜索用时 19 毫秒
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Patricia C. Dykes MA PhD RN Srijesa Khasnabish BA Lesley E. Adkison MSN PhD David W. Bates Michael Bogaisky Zoe Burns MPH Diane L. Carroll MSN PhD Eileen Carter MPhil PhD Ann C. Hurley DNSc Emily Jackson MBOE Susan S. Kurian EdD Mary Ellen Lindros EdD Virginia Ryan MSN Maureen Scanlan MSN Linda Spivack MS Mary-Ann Walsh BSN Jason Adelman 《Journal of the American Geriatrics Society》2021,69(12):3595-3601
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Shira H. Fischer MD PhD Regina A. Shih PhD Tara L. McMullen PhD Maria O. Edelen PhD Sangeeta C. Ahluwalia PhD Emily K. Chen PhD Sarah E. Dalton MA Susan Paddock PhD Anthony Rodriguez PhD Debra Saliba MD MPH AGSF Stella Mandl BSW BSN RN Teresa Mota BSN RN Advisory Group on Medication Reconciliation in PAC 《Journal of the American Geriatrics Society》2022,70(4):1047-1056
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Yuling Wu Jia J. Li Hyun Jun Kim Xu Liu Weiyi Liu Ahmad Akhgar Michael A. Bowen Susan Spitz Xu-Rong Jiang Lorin K. Roskos Wendy I. White 《The AAPS journal》2015,17(6):1417-1426
Benralizumab is a humanized anti-IL5 receptor α (IL5Rα) monoclonal antibody (mAb) with enhanced (afucosylation) antibody-dependent cell-mediated cytotoxicity (ADCC) function. An ADCC reporter cell-based neutralizing antibody (NAb) assay was developed and characterized to detect NAb against benralizumab in human serum to support the clinical development of benralizumab. The optimal ratio of target cells to effector cells was 3:1. Neither parental benralizumab (fucosylated) nor benralizumab Fab resulted in ADCC activity, confirming the requirement for ADCC activity in the NAb assay. The serum tolerance of the cells was determined to be 2.5%. The cut point derived from normal and asthma serum samples was comparable. The effective range of benralizumab was determined, and 35 ng/mL [80% maximal effective concentration (EC80)] was chosen as the standard concentration to run in the assessment of NAb. An affinity purified goat anti-benralizumab polyclonal idiotype antibody preparation was shown to have NAb since it inhibited ADCC activity in a dose-dependent fashion. The low endogenous concentrations of IL5 and soluble IL5 receptor (sIL5R) did not demonstrate to interfere with the assay. The estimated assay sensitivities at the cut point were 1.02 and 1.10 μg/mL as determined by the surrogate neutralizing goat polyclonal and mouse monoclonal anti-drug antibody (ADA) controls, respectively. The assay can detect NAb (at 2.5 μg/mL) in the presence of 0.78 μg/mL benralizumab. The assay was not susceptible to non-specific matrix effects. This study provides an approach and feasibility of developing an ADCC cell-based NAb assay to support biopharmaceuticals with an ADCC function.KEY WORDS: ADCC, benralizumab, cell-based assay, mechanism of action, neutralizing antibody 相似文献
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Wang Grace Karimi Neda Willmann Laura Pipicella Joseph Descallar Joseph OConnor Katie Peculis Luiza Leung Yvette Connor Susan Huang Vivian Williams Astrid-Jane 《Digestive diseases and sciences》2022,67(9):4303-4314
Digestive Diseases and Sciences - Women with inflammatory bowel disease (IBD) with poor IBD-specific reproductive knowledge experience more childlessness and fear of IBD medications in pregnancy.... 相似文献
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