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SARS-CoV-2 accessory proteins reveal distinct serological signatures in children
by
Cheng, Samuel M. S.
, Kwan, Mike Y. W.
, Mok, Chris K. P.
, Ma, Fionn N. L.
, Valkenburg, Sophie A.
, Gu, Haogao
, Qavi, Abraham J.
, Kavian, Niloufar
, Tsang, Owen T. Y.
, Chan, Wai Hung
, Yau, Yat Sun
, Mori, Masashi
, Lau, Eric H. Y.
, Chiu, Susan S.
, Kavian, Otared
, Poon, Leo L. M.
, Hachim, Asmaa
, Peiris, J. S. Malik
, Hui, David S. C.
, Amarasinghe, Gaya K.
in
13/1
/ 13/106
/ 13/109
/ 13/21
/ 631/250/2152
/ 631/250/255
/ 82/80
/ Adult
/ Adults
/ Antibodies
/ Antibody response
/ Antibody Specificity
/ Antigens
/ Asymptomatic
/ Child
/ Children
/ COVID-19
/ Cytokines
/ Humanities and Social Sciences
/ Humans
/ Immunoglobulin G
/ Infections
/ Interleukin 6
/ Interleukin 8
/ Life Sciences
/ Monocyte chemoattractant protein 1
/ Morbidity
/ multidisciplinary
/ Pediatrics
/ Priming
/ Principal components analysis
/ Proteins
/ SARS-CoV-2
/ Science
/ Science (multidisciplinary)
/ Serology
/ Severe acute respiratory syndrome coronavirus 2
/ Signatures
/ Structural proteins
2022
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SARS-CoV-2 accessory proteins reveal distinct serological signatures in children
by
Cheng, Samuel M. S.
, Kwan, Mike Y. W.
, Mok, Chris K. P.
, Ma, Fionn N. L.
, Valkenburg, Sophie A.
, Gu, Haogao
, Qavi, Abraham J.
, Kavian, Niloufar
, Tsang, Owen T. Y.
, Chan, Wai Hung
, Yau, Yat Sun
, Mori, Masashi
, Lau, Eric H. Y.
, Chiu, Susan S.
, Kavian, Otared
, Poon, Leo L. M.
, Hachim, Asmaa
, Peiris, J. S. Malik
, Hui, David S. C.
, Amarasinghe, Gaya K.
in
13/1
/ 13/106
/ 13/109
/ 13/21
/ 631/250/2152
/ 631/250/255
/ 82/80
/ Adult
/ Adults
/ Antibodies
/ Antibody response
/ Antibody Specificity
/ Antigens
/ Asymptomatic
/ Child
/ Children
/ COVID-19
/ Cytokines
/ Humanities and Social Sciences
/ Humans
/ Immunoglobulin G
/ Infections
/ Interleukin 6
/ Interleukin 8
/ Life Sciences
/ Monocyte chemoattractant protein 1
/ Morbidity
/ multidisciplinary
/ Pediatrics
/ Priming
/ Principal components analysis
/ Proteins
/ SARS-CoV-2
/ Science
/ Science (multidisciplinary)
/ Serology
/ Severe acute respiratory syndrome coronavirus 2
/ Signatures
/ Structural proteins
2022
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SARS-CoV-2 accessory proteins reveal distinct serological signatures in children
by
Cheng, Samuel M. S.
, Kwan, Mike Y. W.
, Mok, Chris K. P.
, Ma, Fionn N. L.
, Valkenburg, Sophie A.
, Gu, Haogao
, Qavi, Abraham J.
, Kavian, Niloufar
, Tsang, Owen T. Y.
, Chan, Wai Hung
, Yau, Yat Sun
, Mori, Masashi
, Lau, Eric H. Y.
, Chiu, Susan S.
, Kavian, Otared
, Poon, Leo L. M.
, Hachim, Asmaa
, Peiris, J. S. Malik
, Hui, David S. C.
, Amarasinghe, Gaya K.
in
13/1
/ 13/106
/ 13/109
/ 13/21
/ 631/250/2152
/ 631/250/255
/ 82/80
/ Adult
/ Adults
/ Antibodies
/ Antibody response
/ Antibody Specificity
/ Antigens
/ Asymptomatic
/ Child
/ Children
/ COVID-19
/ Cytokines
/ Humanities and Social Sciences
/ Humans
/ Immunoglobulin G
/ Infections
/ Interleukin 6
/ Interleukin 8
/ Life Sciences
/ Monocyte chemoattractant protein 1
/ Morbidity
/ multidisciplinary
/ Pediatrics
/ Priming
/ Principal components analysis
/ Proteins
/ SARS-CoV-2
/ Science
/ Science (multidisciplinary)
/ Serology
/ Severe acute respiratory syndrome coronavirus 2
/ Signatures
/ Structural proteins
2022
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SARS-CoV-2 accessory proteins reveal distinct serological signatures in children
Journal Article
SARS-CoV-2 accessory proteins reveal distinct serological signatures in children
2022
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Overview
The antibody response magnitude and kinetics may impact clinical severity, serological diagnosis and long-term protection of COVID-19, which may play a role in why children experience lower morbidity. We therefore tested samples from 122 children in Hong Kong with symptomatic (
n
= 78) and asymptomatic (
n
= 44) SARS-CoV-2 infections up to 200 days post infection, relative to 71 infected adults (symptomatic
n
= 61, and asymptomatic
n
= 10), and negative controls (
n
= 48). We assessed serum IgG antibodies to a 14-wide antigen panel of structural and accessory proteins by Luciferase Immuno-Precipitation System (LIPS) assay and circulating cytokines. Infected children have lower levels of Spike, Membrane, ORF3a, ORF7a, ORF7b antibodies, comparable ORF8 and elevated E-specific antibodies than adults. Combination of two unique antibody targets, ORF3d and ORF8, can accurately discriminate SARS-CoV-2 infection in children. Principal component analysis reveals distinct pediatric serological signatures, and the highest contribution to variance from adults are antibody responses to non-structural proteins ORF3d, NSP1, ORF3a and ORF8. From a diverse panel of cytokines that can modulate immune priming and relative inflammation, IL-8, MCP-1 and IL-6 correlate with the magnitude of pediatric antibody specificity and severity. Antibodies to SARS-CoV-2 internal proteins may become an important sero surveillance tool of infection with the roll-out of vaccines in the pediatric population.
The antibody response of children to SARS-CoV-2 is less well studied than in adults. Here Hachim et al. show that children have reduced antibody levels to structural proteins and suggest that the predominance of antibody responses to non-structural proteins can be used to discriminate infection and vaccination.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
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