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

Author:

Watanabe Yoshiyuki12345ORCID,Yamamoto Hiroyuki36ORCID,Matsuba Ikuro1,Watanabe Karin2,Kunishima Tomoyuki1,Takechi Yukako1,Takuma Tetsuo1,Araki Yasushi1,Hirotsu Nobuo1,Sakai Hiroyuki1,Oikawa Ritsuko3,Danno Hiroki7,Fukuda Masakazu7,Sugino Ryuichi7,Futagami Seiji4,Wada Kota5,Itoh Fumio3,Tateishi Keisuke3,Oda Ichiro2,Hatori Yutaka1,Degawa Hisakazu1

Affiliation:

1. Kawasaki Physicians Association Kawasaki Japan

2. Department of Internal Medicine Kawasaki Rinko General Hospital Kawasaki Japan

3. Department of Gastroenterology St. Marianna University School of Medicine Kawasaki Japan

4. Department of Internal Medicine, Division of Gastroenterology Nippon Medical School Tokyo Japan

5. Department of Otorhinolaryngology Toho University Omori Medical Center Tokyo Japan

6. Department of Bioinformatics St. Marianna University Graduate School of Medicine Kanagawa Japan

7. Knowledge Palette Co. Ltd. Kawasaki Japan

Abstract

AbstractMessenger 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.

Publisher

Wiley

Subject

Infectious Diseases,Virology

Reference31 articles.

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