Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines.

COVID-19 SARS-CoV-2 SARS-CoV-2 vaccination T-cells antibodies duration heterologous humoral response immune response immunity immunology

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
24 Feb 2022
Historique:
received: 02 02 2022
revised: 20 02 2022
accepted: 21 02 2022
entrez: 26 3 2022
pubmed: 27 3 2022
medline: 27 3 2022
Statut: epublish

Résumé

Heterologous primary immunization against SARS-CoV-2 is part of applied recommendations. However, little is known about duration of immune responses after heterologous vaccine regimens. To evaluate duration of immune responses after primary vaccination with homologous adeno-vectored ChAdOx1 nCoV-19 vaccine (ChAd) or heterologous ChAd/BNT162b2 mRNA vaccine (BNT), anti-spike-IgG and SARS-CoV-2 VOC-neutralizing antibody responses were measured in 354 healthcare workers (HCW) at 2 weeks, 3 months, 5 months and 6 months after the second vaccine dose. T-cell responses were investigated using a whole blood interferon gamma (IFN-γ) release assay 2 weeks and 3 months post second vaccine dose. Two hundred and ten HCW immunized with homologous BNT were enrolled for comparison of antibody responses. In study participants naïve to SARS-CoV-2 prior to vaccination, heterologous ChAd/BNT resulted in 6-fold higher peak anti-spike IgG antibody titers compared to homologous ChAd vaccination. The half-life of antibody titers was 3.1 months (95% CI 2.8-3.6) following homologous ChAd vaccination and 1.9 months (95% CI 1.7-2.1) after heterologous vaccination, reducing the GMT difference between the groups to 3-fold 6 months post vaccination. Peak T-cell responses were stronger in ChAd/BNT vaccinees, but no significant difference was observed 3 months post vaccination. SARS-CoV-2 infection prior to vaccination resulted in substantially higher peak GMTs and IFN-γ levels and enhanced SARS-CoV-2 specific antibody and T cell responses over time. Heterologous primary SARS-CoV-2 immunization with ChAd and BNT elicits a stronger initial immune response compared to homologous vaccination with ChAd. However, although the differences in humoral responses remain over 6 months, the difference in SARS-CoV-2 specific T cell responses are no longer significant three months after vaccination.

Identifiants

pubmed: 35334989
pii: vaccines10030359
doi: 10.3390/vaccines10030359
pmc: PMC8953845
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Knut and Alice Wallenberg Foundation
Organisme : Jonas and Kristina af Jochnick Foundation
Organisme : Leif Lundblad Family Foundation
Organisme : Swedish Research Council
Organisme : Region Stockholm

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Auteurs

Ulrika Marking (U)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, 182 88 Stockholm, Sweden.

Sebastian Havervall (S)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, 182 88 Stockholm, Sweden.

Nina Greilert-Norin (N)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, 182 88 Stockholm, Sweden.

Henry Ng (H)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, 182 88 Stockholm, Sweden.
Department of Medical Cell Biology, Uppsala University, 751 23 Uppsala, Sweden.

Kim Blom (K)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, 182 88 Stockholm, Sweden.
Department of Microbiology, Public Health Agency of Sweden, 171 82 Solna, Sweden.

Peter Nilsson (P)

Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, 114 28 Stockholm, Sweden.

Mia Phillipson (M)

Department of Medical Cell Biology, Uppsala University, 751 23 Uppsala, Sweden.

Sophia Hober (S)

Department of Protein Science, KTH Royal Institute of Technology, SciLifeLab, 114 28 Stockholm, Sweden.

Charlotta Nilsson (C)

Department of Microbiology, Public Health Agency of Sweden, 171 82 Solna, Sweden.
Division of Clinical Microbiology, Department of Laboratory Medicine, Karolinska Institutet, 171 76 Stockholm, Sweden.

Sara Mangsbo (S)

Department of Pharmacy, SciLifeLab, Uppsala University, 751 23 Uppsala, Sweden.

Wanda Christ (W)

Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, 141 52 Stockholm, Sweden.

Jonas Klingström (J)

Department of Microbiology, Public Health Agency of Sweden, 171 82 Solna, Sweden.
Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, 141 52 Stockholm, Sweden.

Max Gordon (M)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, 182 88 Stockholm, Sweden.

Mikael Åberg (M)

Department of Medical Sciences, Clinical Chemistry, SciLifeLab, Uppsala University, 753 09 Uppsala, Sweden.

Charlotte Thålin (C)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, 182 88 Stockholm, Sweden.

Classifications MeSH