Transcriptomic Analysis Reveals Sixteen Potential Genes Associated with the Successful Differentiation of Antibody-Secreting Cells through the Utilization of Unfolded Protein Response Mechanisms in Robust Responders to the Influenza Vaccine.

B cell response causal genes humoral immune response influenza vaccine response influenza vaccines transcriptomic analysis

Journal

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

Informations de publication

Date de publication:
29 Jan 2024
Historique:
received: 29 12 2023
revised: 23 01 2024
accepted: 26 01 2024
medline: 24 2 2024
pubmed: 24 2 2024
entrez: 24 2 2024
Statut: epublish

Résumé

The seasonal influenza vaccine remains one of the vital recommended infection control measures for the elderly with chronic illnesses. We investigated the immunogenicity of a single dose of influenza vaccine in 123 seronegative participants and classified them into four distinct groups, determined by the promptness of vaccine response, the longevity of humoral immunity, and the likelihood of exhibiting cross-reactivity. Subsequently, we used transcriptional profiling and differential gene expression analysis to identify potential genes directly associated with the robust response to the vaccine. The group of exemplary vaccine responders differentially expressed 16 genes, namely: MZB1, MYDGF, TXNDC5, TXNDC11, HSP90B1, FKBP11, PDIA5, PRDX4, CD38, SDC1, TNFRSF17, TNFRSF13B, PAX5, POU2AF1, IRF4, and XBP1. Our findings point out a list of expressed proteins that are related to B cell proliferation, unfolded protein response, and cellular haemostasis, as well as a linkage of these expressions to the survival of long-lived plasma cells.

Identifiants

pubmed: 38400120
pii: vaccines12020136
doi: 10.3390/vaccines12020136
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : French Government's Investissement d'Avenir program, Laboratoire d'Excellence "Integrative Biology of Emerging Infectious Diseases"
ID : ANR-10-LABX-62-IBEID

Auteurs

Ahmed Tawfik (A)

Functional Genetics of Infectious Diseases Unit, Institut Pasteur, CNRS UMR2000, 75015 Paris, France.
Pasteur International Unit at Center for Genomic Medicine, Kyoto University, Kyoto 606-8507, Japan.

Takahisa Kawaguchi (T)

Center for Genomic Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Meiko Takahashi (M)

Center for Genomic Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Kazuya Setoh (K)

Center for Genomic Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Izumi Yamaguchi (I)

Center for Genomic Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Yasuharu Tabara (Y)

Center for Genomic Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Kristel Van Steen (K)

BIO3-Laboratory for Systems Genetics, GIGA-R Medical Genomics, University of Liège, 4000 Liège, Belgium.
BIO3-Laboratory for Systems Genetics, GIGA-R Medical Genomics, University of Leuven, 3000 Leuven, Belgium.

Anavaj Sakuntabhai (A)

Pasteur International Unit at Center for Genomic Medicine, Kyoto University, Kyoto 606-8507, Japan.
Ecology and Emergence of Arthropod-Borne Pathogens Unit, Institut Pasteur, CNRS UMR2000, 75015 Paris, France.

Fumihiko Matsuda (F)

Center for Genomic Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

Classifications MeSH