Robust and prototypical immune responses toward COVID-19 vaccine in First Nations peoples are impacted by comorbidities.

High-risk groups, including Indigenous people, are at risk of severe COVID-19. Here we found that Australian First Nations peoples elicit effective immune responses to COVID-19 BNT162b2 vaccination, including neutralizing antibodies, receptor-binding domain (RBD) antibodies, SARS-CoV-2 spike-specifi...

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Published in:Nature Immunology
Main Authors: Zhang, W, Kedzierski, L, Chua, B, Mayo, M, Lonzi, C, Rigas, V, Middleton, B, McQuilten, H, Rowntree, L, Allen, L, Purcell, R, Tan, H, Petersen, J, Chaurasia, P, Mordant, F, Pogorelyy, M, Minervina, A, Crawford, J, Perkins, G, Zhang, E, Gras, S, Clemens, E, Juno, J, Audsley, J, Khoury, D, Holmes, N, Thevarajan, I, Subbarao, K, Krammer, F, Cheng, A, Davenport, M, Grubor-Bauk, B, Coates, P, Christensen, B, Thomas, P, Wheatley, A, Kent, S, Rossjohn, J, Chung, A, Boffa, J, Miller, A, Lynar, S, Nelson, J, Nguyen, T, Davies, J, Kedzierska, K
Format: Article in Journal/Newspaper
Language:English
Published: United States 2023
Subjects:
Online Access:https://hdl.handle.net/10137/12471
https://doi.org/10.1038/s41590-023-01508-y
https://www.ezpdhcs.nt.gov.au/login?url=https://www.ncbi.nlm.nih.gov/pubmed/37248417
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description High-risk groups, including Indigenous people, are at risk of severe COVID-19. Here we found that Australian First Nations peoples elicit effective immune responses to COVID-19 BNT162b2 vaccination, including neutralizing antibodies, receptor-binding domain (RBD) antibodies, SARS-CoV-2 spike-specific B cells, and CD4(+) and CD8(+) T cells. In First Nations participants, RBD IgG antibody titers were correlated with body mass index and negatively correlated with age. Reduced RBD antibodies, spike-specific B cells and follicular helper T cells were found in vaccinated participants with chronic conditions (diabetes, renal disease) and were strongly associated with altered glycosylation of IgG and increased interleukin-18 levels in the plasma. These immune perturbations were also found in non-Indigenous people with comorbidities, indicating that they were related to comorbidities rather than ethnicity. However, our study is of a great importance to First Nations peoples who have disproportionate rates of chronic comorbidities and provides evidence of robust immune responses after COVID-19 vaccination in Indigenous people. Department of Microbiology and Immunology, University of Melbourne, at the Peter Doherty Institute for Infection and Immunity, Parkville, Victoria, Australia. Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Melbourne, Victoria, Australia. Menzies School of Health Research, Darwin, Northern Territory, Australia. Infection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia. Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN, USA. Central and Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, South Australia, Australia. Adelaide Medical School, University of Adelaide, Adelaide, South Australia, Australia. Department of Gastroenterology, Royal Melbourne Hospital, Melbourne, Victoria, Australia. ...
format Article in Journal/Newspaper
author Zhang, W
Kedzierski, L
Chua, B
Mayo, M
Lonzi, C
Rigas, V
Middleton, B
McQuilten, H
Rowntree, L
Allen, L
Purcell, R
Tan, H
Petersen, J
Chaurasia, P
Mordant, F
Pogorelyy, M
Minervina, A
Crawford, J
Perkins, G
Zhang, E
Gras, S
Clemens, E
Juno, J
Audsley, J
Khoury, D
Holmes, N
Thevarajan, I
Subbarao, K
Krammer, F
Cheng, A
Davenport, M
Grubor-Bauk, B
Coates, P
Christensen, B
Thomas, P
Wheatley, A
Kent, S
Rossjohn, J
Chung, A
Boffa, J
Miller, A
Lynar, S
Nelson, J
Nguyen, T
Davies, J
Kedzierska, K
spellingShingle Zhang, W
Kedzierski, L
Chua, B
Mayo, M
Lonzi, C
Rigas, V
Middleton, B
McQuilten, H
Rowntree, L
Allen, L
Purcell, R
Tan, H
Petersen, J
Chaurasia, P
Mordant, F
Pogorelyy, M
Minervina, A
Crawford, J
Perkins, G
Zhang, E
Gras, S
Clemens, E
Juno, J
Audsley, J
Khoury, D
Holmes, N
Thevarajan, I
Subbarao, K
Krammer, F
Cheng, A
Davenport, M
Grubor-Bauk, B
Coates, P
Christensen, B
Thomas, P
Wheatley, A
Kent, S
Rossjohn, J
Chung, A
Boffa, J
Miller, A
Lynar, S
Nelson, J
Nguyen, T
Davies, J
Kedzierska, K
Robust and prototypical immune responses toward COVID-19 vaccine in First Nations peoples are impacted by comorbidities.
author_facet Zhang, W
Kedzierski, L
Chua, B
Mayo, M
Lonzi, C
Rigas, V
Middleton, B
McQuilten, H
Rowntree, L
Allen, L
Purcell, R
Tan, H
Petersen, J
Chaurasia, P
Mordant, F
Pogorelyy, M
Minervina, A
Crawford, J
Perkins, G
Zhang, E
Gras, S
Clemens, E
Juno, J
Audsley, J
Khoury, D
Holmes, N
Thevarajan, I
Subbarao, K
Krammer, F
Cheng, A
Davenport, M
Grubor-Bauk, B
Coates, P
Christensen, B
Thomas, P
Wheatley, A
Kent, S
Rossjohn, J
Chung, A
Boffa, J
Miller, A
Lynar, S
Nelson, J
Nguyen, T
Davies, J
Kedzierska, K
author_sort Zhang, W
title Robust and prototypical immune responses toward COVID-19 vaccine in First Nations peoples are impacted by comorbidities.
title_short Robust and prototypical immune responses toward COVID-19 vaccine in First Nations peoples are impacted by comorbidities.
title_full Robust and prototypical immune responses toward COVID-19 vaccine in First Nations peoples are impacted by comorbidities.
title_fullStr Robust and prototypical immune responses toward COVID-19 vaccine in First Nations peoples are impacted by comorbidities.
title_full_unstemmed Robust and prototypical immune responses toward COVID-19 vaccine in First Nations peoples are impacted by comorbidities.
title_sort robust and prototypical immune responses toward covid-19 vaccine in first nations peoples are impacted by comorbidities.
publisher United States
publishDate 2023
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op_relation © 2023. The Author(s).
Nat Immunol. 2023 Jun;24(6):966-978. doi:10.1038/s41590-023-01508-y. Epub 2023 May 29.
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spelling ftnorthernterhls:oai:digitallibrary.health.nt.gov.au:10137/12471 2023-06-18T03:40:37+02:00 Robust and prototypical immune responses toward COVID-19 vaccine in First Nations peoples are impacted by comorbidities. Zhang, W Kedzierski, L Chua, B Mayo, M Lonzi, C Rigas, V Middleton, B McQuilten, H Rowntree, L Allen, L Purcell, R Tan, H Petersen, J Chaurasia, P Mordant, F Pogorelyy, M Minervina, A Crawford, J Perkins, G Zhang, E Gras, S Clemens, E Juno, J Audsley, J Khoury, D Holmes, N Thevarajan, I Subbarao, K Krammer, F Cheng, A Davenport, M Grubor-Bauk, B Coates, P Christensen, B Thomas, P Wheatley, A Kent, S Rossjohn, J Chung, A Boffa, J Miller, A Lynar, S Nelson, J Nguyen, T Davies, J Kedzierska, K 2023/06 966-978 https://hdl.handle.net/10137/12471 https://doi.org/10.1038/s41590-023-01508-y https://www.ezpdhcs.nt.gov.au/login?url=https://www.ncbi.nlm.nih.gov/pubmed/37248417 eng eng United States © 2023. The Author(s). Nat Immunol. 2023 Jun;24(6):966-978. doi:10.1038/s41590-023-01508-y. Epub 2023 May 29. 100941354 https://hdl.handle.net/10137/12471 Nature immunology doi:10.1038/s41590-023-01508-y orcid:0000-0001-7460-4956 orcid:0000-0003-0203-1057 orcid:0000-0002-7089-5300 orcid:0000-0001-6378-5114 orcid:0000-0003-1064-3934 orcid:0000-0002-3755-159X orcid:0000-0002-3754-2642 orcid:0000-0003-4096-6048 orcid:0000-0001-8559-5872 orcid:0000-0001-7416-038X orcid:0000-0002-9072-1017 orcid:0000-0002-2663-1551 orcid:0000-0003-4121-776X orcid:0000-0002-4751-1831 orcid:0000-0001-7955-0256 orcid:0000-0002-5593-9387 orcid:0000-0002-8539-4891 orcid:0000-0002-2020-7522 orcid:0000-0003-0020-9704 orcid:0000-0002-9294-7693 orcid:0000-0002-3843-837X orcid:0000-0001-6141-335X https://www.ezpdhcs.nt.gov.au/login?url=https://www.ncbi.nlm.nih.gov/pubmed/37248417 24 Journal Article 2023 ftnorthernterhls https://doi.org/10.1038/s41590-023-01508-y 2023-06-05T22:15:57Z High-risk groups, including Indigenous people, are at risk of severe COVID-19. Here we found that Australian First Nations peoples elicit effective immune responses to COVID-19 BNT162b2 vaccination, including neutralizing antibodies, receptor-binding domain (RBD) antibodies, SARS-CoV-2 spike-specific B cells, and CD4(+) and CD8(+) T cells. In First Nations participants, RBD IgG antibody titers were correlated with body mass index and negatively correlated with age. Reduced RBD antibodies, spike-specific B cells and follicular helper T cells were found in vaccinated participants with chronic conditions (diabetes, renal disease) and were strongly associated with altered glycosylation of IgG and increased interleukin-18 levels in the plasma. These immune perturbations were also found in non-Indigenous people with comorbidities, indicating that they were related to comorbidities rather than ethnicity. However, our study is of a great importance to First Nations peoples who have disproportionate rates of chronic comorbidities and provides evidence of robust immune responses after COVID-19 vaccination in Indigenous people. Department of Microbiology and Immunology, University of Melbourne, at the Peter Doherty Institute for Infection and Immunity, Parkville, Victoria, Australia. Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Melbourne, Victoria, Australia. Menzies School of Health Research, Darwin, Northern Territory, Australia. Infection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia. Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN, USA. Central and Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, South Australia, Australia. Adelaide Medical School, University of Adelaide, Adelaide, South Australia, Australia. Department of Gastroenterology, Royal Melbourne Hospital, Melbourne, Victoria, Australia. ... Article in Journal/Newspaper First Nations Northern Territory Government Health Library Services ePublications Clayton ENVELOPE(-64.183,-64.183,-65.167,-65.167) Menzies ENVELOPE(61.911,61.911,-73.437,-73.437) Nature Immunology 24 6 966 978