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
Hauptverfasser: 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.
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container_end_page 288
container_issue 2
container_start_page 279
container_title Nature medicine
container_volume 27
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
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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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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 ; 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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. 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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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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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