Phase 1/2 trial of SARS-CoV-2 vaccine ChAdOx1 nCoV-19 with a booster dose induces multifunctional antibody responses
More than 190 vaccines are currently in development to prevent infection by the novel severe acute respiratory syndrome coronavirus 2. Animal studies suggest that while neutralizing antibodies against the viral spike protein may correlate with protection, additional antibody functions may also be im...
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Veröffentlicht in: | Nature medicine 2021-02, Vol.27 (2), p.279-288 |
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creator | Barrett, Jordan R. Belij-Rammerstorfer, Sandra Dold, Christina Ewer, Katie J. Folegatti, Pedro M. Gilbride, Ciaran Halkerston, Rachel Hill, Jennifer Jenkin, Daniel Stockdale, Lisa Verheul, Marije K. Aley, Parvinder K. Angus, Brian Bellamy, Duncan Berrie, Eleanor Bibi, Sagida Bittaye, Mustapha Carroll, Miles W. Cavell, Breeze Clutterbuck, Elizabeth A. Edwards, Nick Flaxman, Amy Fuskova, Michelle Gorringe, Andrew Hallis, Bassam Kerridge, Simon Lawrie, Alison M. Linder, Aline Liu, Xinxue Madhavan, Meera Makinson, Rebecca Mellors, Jack Minassian, Angela Moore, Maria Mujadidi, Yama Plested, Emma Poulton, Ian Ramasamy, Maheshi N. Robinson, Hannah Rollier, Christine S. Song, Rinn Snape, Matthew D. Tarrant, Richard Taylor, Stephen Thomas, Kelly M. Voysey, Merryn Watson, Marion E. E. Wright, Daniel Douglas, Alexander D. Green, Catherine M. Hill, Adrian V. S. Lambe, Teresa Gilbert, Sarah Pollard, Andrew J. |
description | More than 190 vaccines are currently in development to prevent infection by the novel severe acute respiratory syndrome coronavirus 2. Animal studies suggest that while neutralizing antibodies against the viral spike protein may correlate with protection, additional antibody functions may also be important in preventing infection. Previously, we reported early immunogenicity and safety outcomes of a viral vector coronavirus vaccine, ChAdOx1 nCoV-19 (AZD1222), in a single-blinded phase 1/2 randomized controlled trial of healthy adults aged 18–55 years (
NCT04324606
). Now we describe safety and exploratory humoral and cellular immunogenicity of the vaccine, from subgroups of volunteers in that trial, who were subsequently allocated to receive a homologous full-dose (SD/SD D56;
n
= 20) or half-dose (SD/LD D56;
n
= 32) ChAdOx1 booster vaccine 56 d following prime vaccination. Previously reported immunogenicity data from the open-label 28-d interval prime-boost group (SD/SD D28;
n
= 10) are also presented to facilitate comparison. Additionally, we describe volunteers boosted with the comparator vaccine (MenACWY;
n
= 10). In this interim report, we demonstrate that a booster dose of ChAdOx1 nCoV-19 is safe and better tolerated than priming doses. Using a systems serology approach we also demonstrate that anti-spike neutralizing antibody titers, as well as Fc-mediated functional antibody responses, including antibody-dependent neutrophil/monocyte phagocytosis, complement activation and natural killer cell activation, are substantially enhanced by a booster dose of vaccine. A booster dose of vaccine induced stronger antibody responses than a dose-sparing half-dose boost, although the magnitude of T cell responses did not increase with either boost dose. These data support the two-dose vaccine regime that is now being evaluated in phase 3 clinical trials.
Two doses of the coronavirus disease 2019 vaccine ChAdOx1 nCoV-19 boost antibody responses and functions in phase 1/2 trial participants. |
doi_str_mv | 10.1038/s41591-020-01179-4 |
format | Article |
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NCT04324606
). Now we describe safety and exploratory humoral and cellular immunogenicity of the vaccine, from subgroups of volunteers in that trial, who were subsequently allocated to receive a homologous full-dose (SD/SD D56;
n
= 20) or half-dose (SD/LD D56;
n
= 32) ChAdOx1 booster vaccine 56 d following prime vaccination. Previously reported immunogenicity data from the open-label 28-d interval prime-boost group (SD/SD D28;
n
= 10) are also presented to facilitate comparison. Additionally, we describe volunteers boosted with the comparator vaccine (MenACWY;
n
= 10). In this interim report, we demonstrate that a booster dose of ChAdOx1 nCoV-19 is safe and better tolerated than priming doses. Using a systems serology approach we also demonstrate that anti-spike neutralizing antibody titers, as well as Fc-mediated functional antibody responses, including antibody-dependent neutrophil/monocyte phagocytosis, complement activation and natural killer cell activation, are substantially enhanced by a booster dose of vaccine. A booster dose of vaccine induced stronger antibody responses than a dose-sparing half-dose boost, although the magnitude of T cell responses did not increase with either boost dose. These data support the two-dose vaccine regime that is now being evaluated in phase 3 clinical trials.
Two doses of the coronavirus disease 2019 vaccine ChAdOx1 nCoV-19 boost antibody responses and functions in phase 1/2 trial participants.</description><identifier>ISSN: 1078-8956</identifier><identifier>EISSN: 1546-170X</identifier><identifier>DOI: 10.1038/s41591-020-01179-4</identifier><identifier>PMID: 33335322</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/250/590 ; 692/308/2779/777 ; 692/699/255/2514 ; Adolescent ; Adult ; Antibodies ; Antibodies, Neutralizing - immunology ; Antibody Formation - immunology ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Cell activation ; ChAdOx1 nCoV-19 ; Clinical trials ; Complement activation ; Coronaviridae ; Coronaviruses ; COVID-19 ; COVID-19 - immunology ; COVID-19 Vaccines - immunology ; Dose-Response Relationship, Drug ; Genetic Vectors - immunology ; Health aspects ; Homology ; Humans ; Immune response ; Immunization, Secondary ; Immunogenicity ; Infectious Diseases ; Leukocytes (neutrophilic) ; Lymphocytes ; Lymphocytes T ; Metabolic Diseases ; Middle Aged ; Molecular Medicine ; Monocytes ; Natural killer cells ; Neurosciences ; Neutralizing ; Phagocytosis ; Pharmaceutical industry ; Priming ; Product development ; Respiratory diseases ; Safety ; SARS-CoV-2 - immunology ; Serology ; Severe acute respiratory syndrome coronavirus 2 ; Spike Glycoprotein, Coronavirus - immunology ; Spike protein ; Subgroups ; Time Factors ; Vaccines ; Viral antibodies ; Viral diseases ; Young Adult</subject><ispartof>Nature medicine, 2021-02, Vol.27 (2), p.279-288</ispartof><rights>The Author(s), under exclusive licence to Springer Nature America, Inc. 2020. corrected publication 2021</rights><rights>COPYRIGHT 2021 Nature Publishing Group</rights><rights>The Author(s), under exclusive licence to Springer Nature America, Inc. 2020. corrected publication 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c623t-ff032c26cf5b6e7c52b9837814d43c1b263ab3ca4c006c014ffd50e041e971073</citedby><cites>FETCH-LOGICAL-c623t-ff032c26cf5b6e7c52b9837814d43c1b263ab3ca4c006c014ffd50e041e971073</cites><orcidid>0000-0002-6603-8461 ; 0000-0003-0900-9629 ; 0000-0002-9936-8539 ; 0000-0002-7030-7839 ; 0000-0002-2576-8783 ; 0000-0002-2146-4299 ; 0000-0003-2193-7954 ; 0000-0002-9712-8080 ; 0000-0001-8570-2113 ; 0000-0001-9827-9836 ; 0000-0001-6877-1096 ; 0000-0002-0348-654X ; 0000-0002-6823-9750 ; 0000-0003-0746-1945 ; 0000-0001-7832-9824 ; 0000-0001-7711-897X ; 0000-0001-7361-719X ; 0000-0002-2119-951X ; 0000-0003-3088-310X ; 0000-0001-5330-0240 ; 0000-0002-5410-7562 ; 0000-0002-2342-8531 ; 0000-0002-8114-1838 ; 0000-0003-3598-7784</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41591-020-01179-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41591-020-01179-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33335322$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barrett, Jordan R.</creatorcontrib><creatorcontrib>Belij-Rammerstorfer, Sandra</creatorcontrib><creatorcontrib>Dold, Christina</creatorcontrib><creatorcontrib>Ewer, Katie J.</creatorcontrib><creatorcontrib>Folegatti, Pedro M.</creatorcontrib><creatorcontrib>Gilbride, Ciaran</creatorcontrib><creatorcontrib>Halkerston, Rachel</creatorcontrib><creatorcontrib>Hill, Jennifer</creatorcontrib><creatorcontrib>Jenkin, Daniel</creatorcontrib><creatorcontrib>Stockdale, Lisa</creatorcontrib><creatorcontrib>Verheul, Marije K.</creatorcontrib><creatorcontrib>Aley, Parvinder K.</creatorcontrib><creatorcontrib>Angus, Brian</creatorcontrib><creatorcontrib>Bellamy, Duncan</creatorcontrib><creatorcontrib>Berrie, Eleanor</creatorcontrib><creatorcontrib>Bibi, Sagida</creatorcontrib><creatorcontrib>Bittaye, Mustapha</creatorcontrib><creatorcontrib>Carroll, Miles W.</creatorcontrib><creatorcontrib>Cavell, Breeze</creatorcontrib><creatorcontrib>Clutterbuck, Elizabeth A.</creatorcontrib><creatorcontrib>Edwards, Nick</creatorcontrib><creatorcontrib>Flaxman, Amy</creatorcontrib><creatorcontrib>Fuskova, Michelle</creatorcontrib><creatorcontrib>Gorringe, Andrew</creatorcontrib><creatorcontrib>Hallis, Bassam</creatorcontrib><creatorcontrib>Kerridge, Simon</creatorcontrib><creatorcontrib>Lawrie, Alison M.</creatorcontrib><creatorcontrib>Linder, Aline</creatorcontrib><creatorcontrib>Liu, Xinxue</creatorcontrib><creatorcontrib>Madhavan, Meera</creatorcontrib><creatorcontrib>Makinson, Rebecca</creatorcontrib><creatorcontrib>Mellors, Jack</creatorcontrib><creatorcontrib>Minassian, Angela</creatorcontrib><creatorcontrib>Moore, Maria</creatorcontrib><creatorcontrib>Mujadidi, Yama</creatorcontrib><creatorcontrib>Plested, Emma</creatorcontrib><creatorcontrib>Poulton, Ian</creatorcontrib><creatorcontrib>Ramasamy, Maheshi N.</creatorcontrib><creatorcontrib>Robinson, Hannah</creatorcontrib><creatorcontrib>Rollier, Christine S.</creatorcontrib><creatorcontrib>Song, Rinn</creatorcontrib><creatorcontrib>Snape, Matthew D.</creatorcontrib><creatorcontrib>Tarrant, Richard</creatorcontrib><creatorcontrib>Taylor, Stephen</creatorcontrib><creatorcontrib>Thomas, Kelly M.</creatorcontrib><creatorcontrib>Voysey, Merryn</creatorcontrib><creatorcontrib>Watson, Marion E. E.</creatorcontrib><creatorcontrib>Wright, Daniel</creatorcontrib><creatorcontrib>Douglas, Alexander D.</creatorcontrib><creatorcontrib>Green, Catherine M.</creatorcontrib><creatorcontrib>Hill, Adrian V. S.</creatorcontrib><creatorcontrib>Lambe, Teresa</creatorcontrib><creatorcontrib>Gilbert, Sarah</creatorcontrib><creatorcontrib>Pollard, Andrew J.</creatorcontrib><creatorcontrib>Oxford COVID Vaccine Trial Group</creatorcontrib><creatorcontrib>the Oxford COVID Vaccine Trial Group</creatorcontrib><title>Phase 1/2 trial of SARS-CoV-2 vaccine ChAdOx1 nCoV-19 with a booster dose induces multifunctional antibody responses</title><title>Nature medicine</title><addtitle>Nat Med</addtitle><addtitle>Nat Med</addtitle><description>More than 190 vaccines are currently in development to prevent infection by the novel severe acute respiratory syndrome coronavirus 2. Animal studies suggest that while neutralizing antibodies against the viral spike protein may correlate with protection, additional antibody functions may also be important in preventing infection. Previously, we reported early immunogenicity and safety outcomes of a viral vector coronavirus vaccine, ChAdOx1 nCoV-19 (AZD1222), in a single-blinded phase 1/2 randomized controlled trial of healthy adults aged 18–55 years (
NCT04324606
). Now we describe safety and exploratory humoral and cellular immunogenicity of the vaccine, from subgroups of volunteers in that trial, who were subsequently allocated to receive a homologous full-dose (SD/SD D56;
n
= 20) or half-dose (SD/LD D56;
n
= 32) ChAdOx1 booster vaccine 56 d following prime vaccination. Previously reported immunogenicity data from the open-label 28-d interval prime-boost group (SD/SD D28;
n
= 10) are also presented to facilitate comparison. Additionally, we describe volunteers boosted with the comparator vaccine (MenACWY;
n
= 10). In this interim report, we demonstrate that a booster dose of ChAdOx1 nCoV-19 is safe and better tolerated than priming doses. Using a systems serology approach we also demonstrate that anti-spike neutralizing antibody titers, as well as Fc-mediated functional antibody responses, including antibody-dependent neutrophil/monocyte phagocytosis, complement activation and natural killer cell activation, are substantially enhanced by a booster dose of vaccine. A booster dose of vaccine induced stronger antibody responses than a dose-sparing half-dose boost, although the magnitude of T cell responses did not increase with either boost dose. These data support the two-dose vaccine regime that is now being evaluated in phase 3 clinical trials.
Two doses of the coronavirus disease 2019 vaccine ChAdOx1 nCoV-19 boost antibody responses and functions in phase 1/2 trial participants.</description><subject>631/250/590</subject><subject>692/308/2779/777</subject><subject>692/699/255/2514</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Antibodies</subject><subject>Antibodies, Neutralizing - immunology</subject><subject>Antibody Formation - immunology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Cell activation</subject><subject>ChAdOx1 nCoV-19</subject><subject>Clinical trials</subject><subject>Complement activation</subject><subject>Coronaviridae</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - immunology</subject><subject>COVID-19 Vaccines - immunology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Genetic Vectors - immunology</subject><subject>Health aspects</subject><subject>Homology</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunization, Secondary</subject><subject>Immunogenicity</subject><subject>Infectious Diseases</subject><subject>Leukocytes (neutrophilic)</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Metabolic Diseases</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Monocytes</subject><subject>Natural killer cells</subject><subject>Neurosciences</subject><subject>Neutralizing</subject><subject>Phagocytosis</subject><subject>Pharmaceutical industry</subject><subject>Priming</subject><subject>Product development</subject><subject>Respiratory diseases</subject><subject>Safety</subject><subject>SARS-CoV-2 - immunology</subject><subject>Serology</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Spike Glycoprotein, Coronavirus - immunology</subject><subject>Spike protein</subject><subject>Subgroups</subject><subject>Time Factors</subject><subject>Vaccines</subject><subject>Viral antibodies</subject><subject>Viral diseases</subject><subject>Young Adult</subject><issn>1078-8956</issn><issn>1546-170X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkltrFDEYhgdRbK3-AS8kIAhepM1pTpfLYmuhsNLV4l3IZL7spswka5LR9t-bdat1YRETSMKX533J4S2K15ScUsKbsyho2VJMGMGE0rrF4klxTEtRYVqTr0_zmtQNbtqyOipexHhLCOGkbJ8XRzy3kjN2XKRPaxUB0TOGUrBqQN6g5ex6ief-BjP0XWltHaD5etYv7ihy2zJt0Q-b1kihzvuYIKDeZw_r-klDROM0JGsmp5P1Ljsql2zn-3sUIG68ixBfFs-MGiK8ephPii_nHz7PP-KrxcXlfHaFdcV4wsYQzjSrtCm7Cmpdsq5teN1Q0QuuaccqrjquldCEVJpQYUxfEiCCQlvnu_OT4u3OdxP8twlikrd-CvlMUTLRtII3nLBHaqUGkNYZn4LSo41azqqyrGmdh0zhA9QKHAQ1eAfG5vIef3qAz72H0eqDgvd7gswkuEsrNcUoL5fX_88ubvbZd3-xa1BDWkc_TNvfifsg24E6-BgDGLkJdlThXlIit4GTu8DJHDj5K3BSZNGbhyeeuhH6P5LfCcsA3wExb7kVhMc_-IftT5Z62j4</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Barrett, Jordan R.</creator><creator>Belij-Rammerstorfer, Sandra</creator><creator>Dold, Christina</creator><creator>Ewer, Katie J.</creator><creator>Folegatti, Pedro M.</creator><creator>Gilbride, Ciaran</creator><creator>Halkerston, Rachel</creator><creator>Hill, Jennifer</creator><creator>Jenkin, Daniel</creator><creator>Stockdale, Lisa</creator><creator>Verheul, Marije K.</creator><creator>Aley, Parvinder K.</creator><creator>Angus, Brian</creator><creator>Bellamy, Duncan</creator><creator>Berrie, Eleanor</creator><creator>Bibi, Sagida</creator><creator>Bittaye, Mustapha</creator><creator>Carroll, Miles W.</creator><creator>Cavell, Breeze</creator><creator>Clutterbuck, Elizabeth A.</creator><creator>Edwards, Nick</creator><creator>Flaxman, Amy</creator><creator>Fuskova, Michelle</creator><creator>Gorringe, Andrew</creator><creator>Hallis, Bassam</creator><creator>Kerridge, Simon</creator><creator>Lawrie, Alison M.</creator><creator>Linder, Aline</creator><creator>Liu, Xinxue</creator><creator>Madhavan, Meera</creator><creator>Makinson, Rebecca</creator><creator>Mellors, Jack</creator><creator>Minassian, Angela</creator><creator>Moore, Maria</creator><creator>Mujadidi, Yama</creator><creator>Plested, Emma</creator><creator>Poulton, Ian</creator><creator>Ramasamy, Maheshi N.</creator><creator>Robinson, Hannah</creator><creator>Rollier, Christine S.</creator><creator>Song, Rinn</creator><creator>Snape, Matthew D.</creator><creator>Tarrant, Richard</creator><creator>Taylor, Stephen</creator><creator>Thomas, Kelly M.</creator><creator>Voysey, Merryn</creator><creator>Watson, Marion E. 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E. ; Wright, Daniel ; Douglas, Alexander D. ; Green, Catherine M. ; Hill, Adrian V. S. ; Lambe, Teresa ; Gilbert, Sarah ; Pollard, Andrew J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c623t-ff032c26cf5b6e7c52b9837814d43c1b263ab3ca4c006c014ffd50e041e971073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>631/250/590</topic><topic>692/308/2779/777</topic><topic>692/699/255/2514</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Antibodies</topic><topic>Antibodies, Neutralizing - immunology</topic><topic>Antibody Formation - immunology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Cell activation</topic><topic>ChAdOx1 nCoV-19</topic><topic>Clinical trials</topic><topic>Complement activation</topic><topic>Coronaviridae</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>COVID-19 - immunology</topic><topic>COVID-19 Vaccines - immunology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Genetic Vectors - immunology</topic><topic>Health aspects</topic><topic>Homology</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunization, Secondary</topic><topic>Immunogenicity</topic><topic>Infectious Diseases</topic><topic>Leukocytes (neutrophilic)</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Metabolic Diseases</topic><topic>Middle Aged</topic><topic>Molecular Medicine</topic><topic>Monocytes</topic><topic>Natural killer cells</topic><topic>Neurosciences</topic><topic>Neutralizing</topic><topic>Phagocytosis</topic><topic>Pharmaceutical industry</topic><topic>Priming</topic><topic>Product development</topic><topic>Respiratory diseases</topic><topic>Safety</topic><topic>SARS-CoV-2 - immunology</topic><topic>Serology</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Spike Glycoprotein, Coronavirus - immunology</topic><topic>Spike protein</topic><topic>Subgroups</topic><topic>Time Factors</topic><topic>Vaccines</topic><topic>Viral antibodies</topic><topic>Viral diseases</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barrett, Jordan R.</creatorcontrib><creatorcontrib>Belij-Rammerstorfer, Sandra</creatorcontrib><creatorcontrib>Dold, Christina</creatorcontrib><creatorcontrib>Ewer, Katie J.</creatorcontrib><creatorcontrib>Folegatti, Pedro M.</creatorcontrib><creatorcontrib>Gilbride, Ciaran</creatorcontrib><creatorcontrib>Halkerston, Rachel</creatorcontrib><creatorcontrib>Hill, Jennifer</creatorcontrib><creatorcontrib>Jenkin, Daniel</creatorcontrib><creatorcontrib>Stockdale, Lisa</creatorcontrib><creatorcontrib>Verheul, Marije K.</creatorcontrib><creatorcontrib>Aley, Parvinder K.</creatorcontrib><creatorcontrib>Angus, Brian</creatorcontrib><creatorcontrib>Bellamy, Duncan</creatorcontrib><creatorcontrib>Berrie, Eleanor</creatorcontrib><creatorcontrib>Bibi, Sagida</creatorcontrib><creatorcontrib>Bittaye, Mustapha</creatorcontrib><creatorcontrib>Carroll, Miles W.</creatorcontrib><creatorcontrib>Cavell, Breeze</creatorcontrib><creatorcontrib>Clutterbuck, Elizabeth A.</creatorcontrib><creatorcontrib>Edwards, Nick</creatorcontrib><creatorcontrib>Flaxman, Amy</creatorcontrib><creatorcontrib>Fuskova, Michelle</creatorcontrib><creatorcontrib>Gorringe, Andrew</creatorcontrib><creatorcontrib>Hallis, Bassam</creatorcontrib><creatorcontrib>Kerridge, Simon</creatorcontrib><creatorcontrib>Lawrie, Alison M.</creatorcontrib><creatorcontrib>Linder, Aline</creatorcontrib><creatorcontrib>Liu, Xinxue</creatorcontrib><creatorcontrib>Madhavan, Meera</creatorcontrib><creatorcontrib>Makinson, Rebecca</creatorcontrib><creatorcontrib>Mellors, Jack</creatorcontrib><creatorcontrib>Minassian, Angela</creatorcontrib><creatorcontrib>Moore, Maria</creatorcontrib><creatorcontrib>Mujadidi, Yama</creatorcontrib><creatorcontrib>Plested, Emma</creatorcontrib><creatorcontrib>Poulton, Ian</creatorcontrib><creatorcontrib>Ramasamy, Maheshi N.</creatorcontrib><creatorcontrib>Robinson, Hannah</creatorcontrib><creatorcontrib>Rollier, Christine S.</creatorcontrib><creatorcontrib>Song, Rinn</creatorcontrib><creatorcontrib>Snape, Matthew D.</creatorcontrib><creatorcontrib>Tarrant, Richard</creatorcontrib><creatorcontrib>Taylor, Stephen</creatorcontrib><creatorcontrib>Thomas, Kelly M.</creatorcontrib><creatorcontrib>Voysey, Merryn</creatorcontrib><creatorcontrib>Watson, Marion E. 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S.</creatorcontrib><creatorcontrib>Lambe, Teresa</creatorcontrib><creatorcontrib>Gilbert, Sarah</creatorcontrib><creatorcontrib>Pollard, Andrew J.</creatorcontrib><creatorcontrib>Oxford COVID Vaccine Trial Group</creatorcontrib><creatorcontrib>the Oxford COVID Vaccine Trial Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences 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R.</au><au>Belij-Rammerstorfer, Sandra</au><au>Dold, Christina</au><au>Ewer, Katie J.</au><au>Folegatti, Pedro M.</au><au>Gilbride, Ciaran</au><au>Halkerston, Rachel</au><au>Hill, Jennifer</au><au>Jenkin, Daniel</au><au>Stockdale, Lisa</au><au>Verheul, Marije K.</au><au>Aley, Parvinder K.</au><au>Angus, Brian</au><au>Bellamy, Duncan</au><au>Berrie, Eleanor</au><au>Bibi, Sagida</au><au>Bittaye, Mustapha</au><au>Carroll, Miles W.</au><au>Cavell, Breeze</au><au>Clutterbuck, Elizabeth A.</au><au>Edwards, Nick</au><au>Flaxman, Amy</au><au>Fuskova, Michelle</au><au>Gorringe, Andrew</au><au>Hallis, Bassam</au><au>Kerridge, Simon</au><au>Lawrie, Alison M.</au><au>Linder, Aline</au><au>Liu, Xinxue</au><au>Madhavan, Meera</au><au>Makinson, Rebecca</au><au>Mellors, Jack</au><au>Minassian, Angela</au><au>Moore, Maria</au><au>Mujadidi, Yama</au><au>Plested, Emma</au><au>Poulton, Ian</au><au>Ramasamy, Maheshi N.</au><au>Robinson, Hannah</au><au>Rollier, Christine S.</au><au>Song, Rinn</au><au>Snape, Matthew D.</au><au>Tarrant, Richard</au><au>Taylor, Stephen</au><au>Thomas, Kelly M.</au><au>Voysey, Merryn</au><au>Watson, Marion E. E.</au><au>Wright, Daniel</au><au>Douglas, Alexander D.</au><au>Green, Catherine M.</au><au>Hill, Adrian V. S.</au><au>Lambe, Teresa</au><au>Gilbert, Sarah</au><au>Pollard, Andrew J.</au><aucorp>Oxford COVID Vaccine Trial Group</aucorp><aucorp>the Oxford COVID Vaccine Trial Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phase 1/2 trial of SARS-CoV-2 vaccine ChAdOx1 nCoV-19 with a booster dose induces multifunctional antibody responses</atitle><jtitle>Nature medicine</jtitle><stitle>Nat Med</stitle><addtitle>Nat Med</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>27</volume><issue>2</issue><spage>279</spage><epage>288</epage><pages>279-288</pages><issn>1078-8956</issn><eissn>1546-170X</eissn><abstract>More than 190 vaccines are currently in development to prevent infection by the novel severe acute respiratory syndrome coronavirus 2. Animal studies suggest that while neutralizing antibodies against the viral spike protein may correlate with protection, additional antibody functions may also be important in preventing infection. Previously, we reported early immunogenicity and safety outcomes of a viral vector coronavirus vaccine, ChAdOx1 nCoV-19 (AZD1222), in a single-blinded phase 1/2 randomized controlled trial of healthy adults aged 18–55 years (
NCT04324606
). Now we describe safety and exploratory humoral and cellular immunogenicity of the vaccine, from subgroups of volunteers in that trial, who were subsequently allocated to receive a homologous full-dose (SD/SD D56;
n
= 20) or half-dose (SD/LD D56;
n
= 32) ChAdOx1 booster vaccine 56 d following prime vaccination. Previously reported immunogenicity data from the open-label 28-d interval prime-boost group (SD/SD D28;
n
= 10) are also presented to facilitate comparison. Additionally, we describe volunteers boosted with the comparator vaccine (MenACWY;
n
= 10). In this interim report, we demonstrate that a booster dose of ChAdOx1 nCoV-19 is safe and better tolerated than priming doses. Using a systems serology approach we also demonstrate that anti-spike neutralizing antibody titers, as well as Fc-mediated functional antibody responses, including antibody-dependent neutrophil/monocyte phagocytosis, complement activation and natural killer cell activation, are substantially enhanced by a booster dose of vaccine. A booster dose of vaccine induced stronger antibody responses than a dose-sparing half-dose boost, although the magnitude of T cell responses did not increase with either boost dose. These data support the two-dose vaccine regime that is now being evaluated in phase 3 clinical trials.
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fulltext | fulltext |
identifier | ISSN: 1078-8956 |
ispartof | Nature medicine, 2021-02, Vol.27 (2), p.279-288 |
issn | 1078-8956 1546-170X |
language | eng |
recordid | cdi_proquest_journals_2489438302 |
source | MEDLINE; Springer Nature - Complete Springer Journals; Nature Journals Online |
subjects | 631/250/590 692/308/2779/777 692/699/255/2514 Adolescent Adult Antibodies Antibodies, Neutralizing - immunology Antibody Formation - immunology Biomedical and Life Sciences Biomedicine Cancer Research Cell activation ChAdOx1 nCoV-19 Clinical trials Complement activation Coronaviridae Coronaviruses COVID-19 COVID-19 - immunology COVID-19 Vaccines - immunology Dose-Response Relationship, Drug Genetic Vectors - immunology Health aspects Homology Humans Immune response Immunization, Secondary Immunogenicity Infectious Diseases Leukocytes (neutrophilic) Lymphocytes Lymphocytes T Metabolic Diseases Middle Aged Molecular Medicine Monocytes Natural killer cells Neurosciences Neutralizing Phagocytosis Pharmaceutical industry Priming Product development Respiratory diseases Safety SARS-CoV-2 - immunology Serology Severe acute respiratory syndrome coronavirus 2 Spike Glycoprotein, Coronavirus - immunology Spike protein Subgroups Time Factors Vaccines Viral antibodies Viral diseases Young Adult |
title | Phase 1/2 trial of SARS-CoV-2 vaccine ChAdOx1 nCoV-19 with a booster dose induces multifunctional antibody responses |
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