Evidence map›Paper›PMID 39835127›Full record

ArticleFrontiers in immunology2024

Single-cell transcriptome atlas of peripheral immune features to Omicron breakthrough infection under booster vaccination strategies.

Yuwei Zhang, Shanshan Han, Qingshuai Sun, Tao Liu, Zixuan Wen, Mingxiao Yao, Shu Zhang, Qing Duan, Xiaomei Zhang, Bo Pang and 2 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yuwei ZhangInfectious Disease Prevention and Control Section, Shandong Center for Disease Control and Prevention, Jinan, Shandong, China.
Shanshan HanSchool of Public Health and Health Management, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Qingshuai SunSchool of Public Health and Health Management, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Tao LiuDepartment of Infectious Disease Control, Yantai Center for Disease Control and Prevention, Yantai, Shandong, China.
Zixuan WenSchool of Public Health, Weifang Medical University, Weifang, Shandong, China.
Mingxiao YaoInfectious Disease Prevention and Control Section, Shandong Center for Disease Control and Prevention, Jinan, Shandong, China.
Shu ZhangInfectious Disease Prevention and Control Section, Shandong Center for Disease Control and Prevention, Jinan, Shandong, China.
Qing DuanInfectious Disease Prevention and Control Section, Shandong Center for Disease Control and Prevention, Jinan, Shandong, China.
Xiaomei ZhangInfectious Disease Prevention and Control Section, Shandong Center for Disease Control and Prevention, Jinan, Shandong, China.
Bo PangInfectious Disease Prevention and Control Section, Shandong Center for Disease Control and Prevention, Jinan, Shandong, China.
Zengqiang KouInfectious Disease Prevention and Control Section, Shandong Center for Disease Control and Prevention, Jinan, Shandong, China.
Xiaolin JiangSchool of Public Health and Health Management, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The high percentage of Omicron breakthrough infection in vaccinees is an emerging problem, of which we have a limited understanding of the phenomenon. Methods: We performed single-cell transcriptome coupled with T-cell/B-cell receptor (TCR/BCR) sequencing in 15 peripheral blood mononuclear cell (PBMC) samples from Omicron infection and naïve with booster vaccination. Results: We found that after breakthrough infection, multiple cell clusters showed activation of the type I IFN pathway and widespread expression of Interferon-stimulated genes (ISGs); T and B lymphocytes exhibited antiviral and proinflammatory-related differentiation features with pseudo-time trajectories; and large TCR clonal expansions were concentrated in effector CD8 T cells, and clonal expansions of BCRs showed a preference for IGHV3. In addition, myeloid cells in the BA.5.2 breakthrough infection with the fourth dose of aerosolized Ad5-nCoV were characterized by enhanced proliferation, chemotactic migration, and antigen presentation. Discussion: Collectively, our study informs the comprehensive understandings of immune characterization for Omicron breakthrough infection, revealing the positive antiviral potential induced by booster doses of vaccine and the possible "trained immunity" phenomenon in the fourth dose of aerosolized Ad5-nCoV, providing a basis for the selection of vaccination strategies.

Indexed as

COVID-19COVID-19 VaccinesImmunization, SecondarySARS-CoV-2TranscriptomeB-LymphocytesBreakthrough InfectionsHumansLeukocytes, MononuclearReceptors, Antigen, B-CellReceptors, Antigen, T-CellSingle-Cell AnalysisVaccinationCOVID-19 VaccinesReceptors, Antigen, B-CellReceptors, Antigen, T-Cellbooster vaccinationbreakthrough infectionCOVID-19Omicronperipheral immune responsesscRNA-seq

Identifiers

PMID39835127
PMCPMC11743671

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.