Comparative Systems Analyses Reveal Molecular Signatures of Clinically tested Vaccine Adjuvants
Journal article, 2016

A better understanding of the mechanisms of action of human adjuvants could inform a rational development of next generation vaccines for human use. Here, we exploited a genome wide transcriptomics analysis combined with a systems biology approach to determine the molecular signatures induced by four clinically tested vaccine adjuvants, namely CAF01, IC31, GLA-SE and Alum in mice. We report signature molecules, pathways, gene modules and networks, which are shared by or otherwise exclusive to these clinical-grade adjuvants in whole blood and draining lymph nodes of mice. Intriguingly, co-expression analysis revealed blood gene modules highly enriched for molecules with documented roles in T follicular helper (TFH) and germinal center (GC) responses. We could show that all adjuvants enhanced, although with different magnitude and kinetics, TFH and GC B cell responses in draining lymph nodes. These results represent, to our knowledge, the first comparative systems analysis of clinically tested vaccine adjuvants that may provide new insights into the mechanisms of action of human adjuvants.

network

expression

tuberculosis vaccine

alum adjuvant

analysis

activation

Science & Technology - Other Topics

generation

dendritic cells

infection

immunity

t-cell responses

Author

T. A. Olafsdottir

Goteborgs universitet, Institutionen for biomedicin

M. Lindqvist

Goteborgs universitet, Institutionen for biomedicin

Intawat Nookaew

Chalmers, Biology and Biological Engineering, Systems and Synthetic Biology

P. Andersen

Statens Serum Institut

J. Maertzdorf

Max Planck Institute for Infection Biology

J. Persson

Goteborgs universitet, Institutionen for biomedicin

D. Christensen

Statens Serum Institut

Y. Zhang

Goteborgs universitet, Institutionen for biomedicin

J. Anderson

Goteborgs universitet, Institutionen for biomedicin

Sakda Khoomrung

Chalmers, Biology and Biological Engineering, Systems and Synthetic Biology

Partho Sen

Chalmers University of Technology

E. M. Agger

Statens Serum Institut

R. Coler

Infectious Disease Research Institute

D. Carter

Infectious Disease Research Institute

A. Meinke

Vienna Biocenter

R. Rappuoli

GSK Vaccines

S. H. E. Kaufmann

Max Planck Institute for Infection Biology

S. G. Reed

Infectious Disease Research Institute

A. M. Harandi

Goteborgs universitet, Institutionen for biomedicin

Scientific Reports

2045-2322 (ISSN)

Vol. 6 39097

Subject Categories (SSIF 2011)

Biocatalysis and Enzyme Technology

Organic Chemistry

DOI

10.1038/srep39097

More information

Created

10/7/2017