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      mRNA vaccination boosts cross-variant neutralizing antibodies elicited by SARS-CoV-2 infection

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          Abstract

          Emerging SARS-CoV-2 variants have raised concerns about resistance to neutralizing antibodies elicited by previous infection or vaccination. We examined whether sera from recovered and nave donors collected prior to, and following immunizations with existing mRNA vaccines, could neutralize the Wuhan-Hu-1 and B.1.351 variants. Pre-vaccination sera from recovered donors neutralized Wuhan-Hu-1 and sporadically neutralized B.1.351, but a single immunization boosted neutralizing titers against all variants and SARS-CoV-1 by up to 1000-fold. Neutralization was due to antibodies targeting the receptor binding domain and was not boosted by a second immunization. Immunization of nave donors also elicited cross-neutralizing responses, but at lower titers. Our study highlights the importance of vaccinating both uninfected and previously infected persons to elicit cross-variant neutralizing antibodies.

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          Most cited references76

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          A Novel Coronavirus from Patients with Pneumonia in China, 2019

          Summary In December 2019, a cluster of patients with pneumonia of unknown cause was linked to a seafood wholesale market in Wuhan, China. A previously unknown betacoronavirus was discovered through the use of unbiased sequencing in samples from patients with pneumonia. Human airway epithelial cells were used to isolate a novel coronavirus, named 2019-nCoV, which formed a clade within the subgenus sarbecovirus, Orthocoronavirinae subfamily. Different from both MERS-CoV and SARS-CoV, 2019-nCoV is the seventh member of the family of coronaviruses that infect humans. Enhanced surveillance and further investigation are ongoing. (Funded by the National Key Research and Development Program of China and the National Major Project for Control and Prevention of Infectious Disease in China.)
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            A pneumonia outbreak associated with a new coronavirus of probable bat origin

            Since the outbreak of severe acute respiratory syndrome (SARS) 18 years ago, a large number of SARS-related coronaviruses (SARSr-CoVs) have been discovered in their natural reservoir host, bats 1–4 . Previous studies have shown that some bat SARSr-CoVs have the potential to infect humans 5–7 . Here we report the identification and characterization of a new coronavirus (2019-nCoV), which caused an epidemic of acute respiratory syndrome in humans in Wuhan, China. The epidemic, which started on 12 December 2019, had caused 2,794 laboratory-confirmed infections including 80 deaths by 26 January 2020. Full-length genome sequences were obtained from five patients at an early stage of the outbreak. The sequences are almost identical and share 79.6% sequence identity to SARS-CoV. Furthermore, we show that 2019-nCoV is 96% identical at the whole-genome level to a bat coronavirus. Pairwise protein sequence analysis of seven conserved non-structural proteins domains show that this virus belongs to the species of SARSr-CoV. In addition, 2019-nCoV virus isolated from the bronchoalveolar lavage fluid of a critically ill patient could be neutralized by sera from several patients. Notably, we confirmed that 2019-nCoV uses the same cell entry receptor—angiotensin converting enzyme II (ACE2)—as SARS-CoV.
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              Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

              Research electronic data capture (REDCap) is a novel workflow methodology and software solution designed for rapid development and deployment of electronic data capture tools to support clinical and translational research. We present: (1) a brief description of the REDCap metadata-driven software toolset; (2) detail concerning the capture and use of study-related metadata from scientific research teams; (3) measures of impact for REDCap; (4) details concerning a consortium network of domestic and international institutions collaborating on the project; and (5) strengths and limitations of the REDCap system. REDCap is currently supporting 286 translational research projects in a growing collaborative network including 27 active partner institutions.
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                Author and article information

                Journal
                Science
                Science
                SCIENCE
                Science (New York, N.y.)
                American Association for the Advancement of Science
                0036-8075
                1095-9203
                25 March 2021
                : eabg9175
                Affiliations
                [1 ]Fred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division, Seattle, WA, USA.
                [2 ]Department of Global Health, University of Washington, Seattle, WA, USA.
                [3 ]Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.
                [4 ]Centre de Recherche du CHUM, Montral, QC, Canada.
                [5 ]Dpartement de Microbiologie, Infectiologie et Immunologie, Universit de Montral, Montreal, QC, Canada.
                [6 ]Department of Microbiology and Immunology, McGill University, Montreal, QC, Canada.
                [7 ]Department of Medicine, University of Washington, Seattle, WA, USA.
                Author notes
                Author information
                https://orcid.org/0000-0002-1106-7097
                https://orcid.org/0000-0002-4344-6390
                https://orcid.org/0000-0003-2826-9928
                https://orcid.org/0000-0001-8421-6519
                https://orcid.org/0000-0003-2134-0576
                https://orcid.org/0000-0002-1017-3488
                https://orcid.org/0000-0002-3154-6597
                https://orcid.org/0000-0003-1021-4056
                https://orcid.org/0000-0001-6633-7413
                https://orcid.org/0000-0001-5552-9209
                https://orcid.org/0000-0003-4680-1893
                https://orcid.org/0000-0003-3871-4618
                https://orcid.org/0000-0002-4992-5288
                https://orcid.org/0000-0002-3530-9310
                https://orcid.org/0000-0002-8901-9941
                https://orcid.org/0000-0001-8701-2001
                https://orcid.org/0000-0003-2276-7117
                https://orcid.org/0000-0003-1841-6859
                Article
                abg9175
                10.1126/science.abg9175
                8139425
                33766944
                1f755af4-a07c-47fb-a4be-859677320788
                Copyright 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY).

                This is an open-access article distributed under the terms of the Creative Commons Attribution license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 04 February 2021
                : 19 March 2021
                Funding
                Funded by: doi http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: UM1 AI068618-14S1
                Funded by: doi http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: 2UM1AI069481-15
                Funded by: doi http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases;
                Award ID: UM1A057266-S1
                Funded by: doi http://dx.doi.org/10.13039/100000952, Paul G. Allen Family Foundation;
                Funded by: doi http://dx.doi.org/10.13039/100005895, Fred Hutchinson Cancer Research Center;
                Funded by: Joel D. Meyers Endowed Chair;
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