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Time‐series transcriptome analysis of peripheral blood mononuclear cells obtained from individuals who received the SARS‐CoV‐2 mRNA vaccine.

Authors :
Watanabe, Yoshiyuki
Yamamoto, Hiroyuki
Matsuba, Ikuro
Watanabe, Karin
Kunishima, Tomoyuki
Takechi, Yukako
Takuma, Tetsuo
Araki, Yasushi
Hirotsu, Nobuo
Sakai, Hiroyuki
Oikawa, Ritsuko
Danno, Hiroki
Fukuda, Masakazu
Sugino, Ryuichi
Futagami, Seiji
Wada, Kota
Itoh, Fumio
Tateishi, Keisuke
Oda, Ichiro
Hatori, Yutaka
Source :
Journal of Medical Virology; Jun2023, Vol. 95 Issue 6, p1-13, 13p
Publication Year :
2023

Abstract

Messenger ribonucleic acid (mRNA) vaccination against coronavirus disease 2019 (COVID‐19) is an effective prevention strategy, despite a limited understanding of the molecular mechanisms underlying the host immune system and individual heterogeneity of the variable effects of mRNA vaccination. We assessed the time‐series changes in the comprehensive gene expression profiles of 200 vaccinated healthcare workers by performing bulk transcriptome and bioinformatics analyses, including dimensionality reduction utilizing the uniform manifold approximation and projection (UMAP) technique. For these analyses, blood samples, including peripheral blood mononuclear cells (PBMCs), were collected from 214 vaccine recipients before vaccination (T1) and on Days 22 (T2, after second dose), 90, 180 (T3, before a booster dose), and 360 (T4, after a booster dose) after receiving the first dose of BNT162b2 vaccine (UMIN000043851). UMAP successfully visualized the main cluster of gene expression at each time point in PBMC samples (T1–T4). Through differentially expressed gene (DEG) analysis, we identified genes that showed fluctuating expression levels and gradual increases in expression levels from T1 to T4, as well as genes with increased expression levels at T4 alone. We also succeeded in dividing these cases into five types based on the changes in gene expression levels. High‐throughput and temporal bulk RNA‐based transcriptome analysis is a useful approach for inclusive, diverse, and cost‐effective large‐scale clinical studies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01466615
Volume :
95
Issue :
6
Database :
Complementary Index
Journal :
Journal of Medical Virology
Publication Type :
Academic Journal
Accession number :
164634800
Full Text :
https://doi.org/10.1002/jmv.28884