mRNA COVID-19 vaccine elicits potent adaptive immune response without the acute inflammation of SARS-CoV-2 infection
Ellie N. Ivanova, Jasmine Shwetar, Joseph C. Devlin, Terkild B. Buus, Sophie Gray-Gaillard, Akiko Koide, Amber Cornelius, Marie I. Samanovic, Alberto Herrera, Eleni P. Mimitou, Chenzhen Zhang, Trishala Karmacharya, Ludovic Desvignes, Niels Ødum, Peter Smibert, Robert J. Ulrich, Mark J. Mulligan, Shohei Koide, Kelly V. Ruggles, Ramin S. Herati, Sergei B. Koralov
Abstract
SARS-CoV-2 infection and vaccination elicit potent immune responses. Our study presents a comprehensive multimodal single-cell analysis of blood from COVID-19 patients and healthy volunteers receiving the SARS-CoV-2 vaccine and booster. We profiled immune responses via transcriptional analysis and lymphocyte repertoire reconstruction. COVID-19 patients displayed an enhanced interferon signature and cytotoxic gene upregulation, absent in vaccine recipients. B and T cell repertoire analysis revealed clonal expansion among effector cells in COVID-19 patients and memory cells in vaccine recipients. Furthermore, while clonal αβ T cell responses were observed in both COVID-19 patients and vaccine recipients, expansion of clonal γδ T cells was found only in infected individuals. Our dataset enables side-by-side comparison of immune responses to infection versus vaccination, including clonal B and T cell responses. Our comparative analysis shows that vaccination induces a robust, durable clonal B and T cell responses, without the severe inflammation associated with infection.
Datasets
1. Circulating Immune cells -- CV19 infection, vaccination and HC
Metadata
BCR_IGH.V.1
BCR_IGH.D.1
BCR_IGH.J.1
BCR_IGH.C.1
BCR_IGL.V.1
BCR_IGL.J.1
BCR_IGL.C.1
BCR_IGK.V.1
BCR_IGK.J.1
BCR_IGK.C.1
TCRab_TRA.V.1
TCRab_TRA.J.1
TCRab_TRA.C.1
TCRab_TRB.V.1
TCRab_TRB.D.1
TCRab_TRB.J.1
TCRab_TRB.C.1
TCRab.top10
TCRgd_TRD.V.1
TCRgd_TRD.J.1
TCRgd_TRD.C.1
TCRgd_TRG.V.1
TCRgd_TRG.J.1
TCRgd_TRG.C.1
Day
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tissue_ontology_term_id
age_group
celltype.final
cell_type_ontology_term_id
celltype.broad_clustering_annot
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sampleName_with_day
cv19_vax_boost_or_HC_status
tissue_type
cell_type
assay
disease
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HsapDv:0000238123181 cells HsapDv:000024039676 cells HsapDv:000023926357 cells NCBITaxon:9606195632 cells HANCESTRO:0008102315 cells HANCESTRO:000579578 cells UBERON:0000178195632 cells NK.Proliferating441 cells NK.Proliferating441 cells cv19_0711_ln2_samples17174 cells cv19_samples_0527_ln215891 cells cv19_samples_0527_ln114402 cells cv19_0714_ln2_samples11460 cells cv19_0711_ln1_samples7321 cells cv19_0714_ln1_samples6137 cells CV-001_d0_booster4633 cells CV-003_d0_booster4049 cells cv19_PBMC_SK-013_d114048 cells cv19_PBMC_SK-014_d93894 cells cv19_PBMC_SK-012_d83762 cells cv19_PBMC_SK-011_d133739 cells cv19_PBMC_SK-012_d24_LB3714 cells CV-011_d120_booster3710 cells CV-003_d7_booster3626 cells cv19_PBMC_SK-010_d123519 cells CV-001_d28_booster3420 cells cv19_PBMC_SK-011_d63409 cells H1N1_PBMC_SK-008_v03099 cells cv19_PBMC_SK-010_d243028 cells cv19_PBMC_SK-012_d8_LB3000 cells CV-011_d7_booster2795 cells CV-003_d28_booster2718 cells CV-011_d0_booster2703 cells CV-001_d7_booster2639 cells cv19_PBMC_SK-012_d242423 cells cv19_PBMC_SK-013_d62370 cells CD4-positive, alpha-beta T cell61350 cells CD8-positive, alpha-beta T cell35752 cells natural killer cell28834 cells gamma-delta T cell3184 cells mucosal invariant T cell1244 cells fourth decade human stage123181 cells sixth decade human stage39676 cells fifth decade human stage26357 cells seventh decade human stage6418 cells Analyze this study
Source data
https://cellxgene.cziscience.com/collections/ecb739c5-fe0d-4b48-81c6-217c4d64eec4
Alias names
GSE247917, PMID38213787, PMC10783604
Cite this study
Ivanova, E.N., Shwetar, J., Devlin, J.C., Buus, T.B., Gray-Gaillard, S., Koide, A., Cornelius, A., Samanovic, M.I., Herrera, A., Mimitou, E.P. and Zhang, C., 2023. mRNA COVID-19 vaccine elicits potent adaptive immune response without the acute inflammation of SARS-CoV-2 infection. Iscience, 26(12). https://doi.org/10.1016/j.isci.2023.108572