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Humoral and cell-mediated immune responses to COVID-19 vaccines up to 6 months post three-dose primary series in adults with inborn errors of immunity and their breakthrough infections.

作者信息

Unninayar Dana, Falcone Emilia L, Chapdelaine Hugo, Vinh Donald C, Top Karina A, Derfalvi Beata, Issekutz Thomas B, Decaluwe Hélène, Pham-Huy Anne, Upton Julia, Betschel Stephen D, Rubin Tamar, Suresh Sneha, Wright Nicola A M, Murguía-Favela Luis, Kalashnikova Tatiana, Barrett Lisa, Oldford Sharon, Langlois Marc-Andre, Arnold Corey, Sadarangani Manish, Zhang Tinghua, Ramsay Tim, Yazji Dina, Cowan Juthaporn

机构信息

Inflammation and Chronic Disease Program, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada.

出版信息

Front Immunol. 2025 Jan 21;15:1501908. doi: 10.3389/fimmu.2024.1501908. eCollection 2024.


DOI:10.3389/fimmu.2024.1501908
PMID:39906736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11790575/
Abstract

PURPOSE: Many individuals with inborn errors of immunity (IEIs) have poor humoral immune (HI) vaccine responses. Only a few studies have examined specific cell-mediated immune (CMI) responses to coronavirus disease 2019 (COVID-19) vaccines in this population. Therefore, the purpose of this study was to examine HI and CMI responses up to 6 months post-COVID-19 vaccine dose 3 in adults with IEIs. METHODS: A multi-center prospective observational study was conducted across Canada to collect severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2)-specific HI and CMI data at 4- and 24-week intervals after vaccine doses 2 and 3 (D2 + 4wk/D2 + 24wk/D3 + 4wk/D3 + 24wk). RESULTS: A total of 149 adults with IEIs and 423 healthy controls were recruited from July 2021 to October 2023. Geometric mean anti-spike IgG (binding antibody units/mL) and spike-specific T-cell responses [IFN-γ T cells/10 peripheral blood mononuclear cells (PBMCs)] were significantly lower in IEIs compared to controls at D2 + 4wk, D3 + 4wk, and D3 + 24wk. However, at 6 months after completing the primary series (three doses for IEIs and two doses for healthy), both HI and CMI responses of both IEI participants and healthy controls persisted and were comparable. There was a strong correlation between neutralizing antibody titer (ID50) and anti-spike IgG but not between ID50 and CMI. There was only one reported case of hospitalized COVID-19 disease before and none after completing the primary series among IEI participants. CONCLUSION: Adults with IEIs mounted both HI and CMI responses following COVID-19 vaccines, which were lower than those of healthy individuals but were present at least up to 6 months after dose 3. These data support the initial recommendation for a three-dose primary series among IEIs.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/16ac5f6c0e5e/fimmu-15-1501908-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/77d22433e9d0/fimmu-15-1501908-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/e79fa566c70e/fimmu-15-1501908-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/3e98b970cb4d/fimmu-15-1501908-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/99cb555cd927/fimmu-15-1501908-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/29aca51a076f/fimmu-15-1501908-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/455f7253b770/fimmu-15-1501908-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/d5c522e8eff4/fimmu-15-1501908-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/00fcd21ac5d0/fimmu-15-1501908-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/16ac5f6c0e5e/fimmu-15-1501908-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/77d22433e9d0/fimmu-15-1501908-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/e79fa566c70e/fimmu-15-1501908-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/3e98b970cb4d/fimmu-15-1501908-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/99cb555cd927/fimmu-15-1501908-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/29aca51a076f/fimmu-15-1501908-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/455f7253b770/fimmu-15-1501908-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/d5c522e8eff4/fimmu-15-1501908-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/00fcd21ac5d0/fimmu-15-1501908-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0950/11790575/16ac5f6c0e5e/fimmu-15-1501908-g009.jpg

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Humoral and cell-mediated immune responses to COVID-19 vaccines up to 6 months post three-dose primary series in adults with inborn errors of immunity and their breakthrough infections.

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本文引用的文献

[1]
Follow-up of immune response in patients with common variable immunodeficiency following SARS-CoV-2 vaccination.

Clin Exp Immunol. 2024-8-9

[2]
Use of an Additional Updated 2023-2024 COVID-19 Vaccine Dose for Adults Aged ≥65 Years: Recommendations of the Advisory Committee on Immunization Practices - United States, 2024.

MMWR Morb Mortal Wkly Rep. 2024-4-25

[3]
SARS-CoV-2 viral clearance and evolution varies by type and severity of immunodeficiency.

Sci Transl Med. 2024-1-24

[4]
Perturbations of the T-cell receptor repertoire in response to SARS-CoV-2 in immunocompetent and immunocompromised individuals.

J Allergy Clin Immunol. 2024-6

[5]
Results of the Stop the Spread Ottawa (SSO) cohort study: a Canadian urban-based prospective evaluation of antibody responses and neutralisation efficiency to SARS-CoV-2 infection and vaccination.

BMJ Open. 2023-10-31

[6]
Characterization of the antispike IgG immune response to COVID-19 vaccines in people with a wide variety of immunodeficiencies.

Sci Adv. 2023-10-13

[7]
Effects of COVID-19 vaccination and previous infection on Omicron SARS-CoV-2 infection and relation with serology.

Nat Commun. 2023-8-9

[8]
Effects of previous infection, vaccination, and hybrid immunity against symptomatic Alpha, Beta, and Delta SARS-CoV-2 infections: an observational study.

EBioMedicine. 2023-9

[9]
Real-world assessment of immunogenicity in immunocompromised individuals following SARS-CoV-2 mRNA vaccination: a one-year follow-up of the prospective clinical trial COVAXID.

EBioMedicine. 2023-8

[10]
Immune Responses 6 Months After mRNA-1273 COVID-19 Vaccination and the Effect of a Third Vaccination in Patients with Inborn Errors of Immunity.

J Clin Immunol. 2023-8

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