Molecular Signature of Monocytes Shaped by the Shigella sonnei 1790-Generalized Modules for Membrane Antigens Vaccine
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Published:2024-01-17
Issue:2
Volume:25
Page:1116
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ISSN:1422-0067
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Container-title:International Journal of Molecular Sciences
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language:en
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Short-container-title:IJMS
Author:
Tondi Serena12, Siena Emilio1, Essaghir Ahmed1, Bozzetti Benoît3, Bechtold Viviane3, Scaillet Aline3, Clemente Bruna1, Marrocco Mariateresa12, Sammicheli Chiara1, Tavarini Simona1, Micoli Francesca4, Oldrini Davide4ORCID, Pezzicoli Alfredo1, Di Fede Martina1, Brazzoli Michela1, Ulivieri Cristina2ORCID, Schiavetti Francesca1
Affiliation:
1. Preclinical Research & Development, GSK, 53100 Siena, Italy 2. Department of Life Sciences, University of Siena, 53100 Siena, Italy 3. Preclinical Research & Development, GSK, 1330 Rixensart, Belgium 4. GSK Vaccines Institute for Global Health S.R.L. (GVGH), 53100 Siena, Italy
Abstract
Shigellosis, an acute gastroenteritis infection caused by Shigella species, remains a public health burden in developing countries. Recently, many outbreaks due to Shigella sonnei multidrug-resistant strains have been reported in high-income countries, and the lack of an effective vaccine represents a major hurdle to counteract this bacterial pathogen. Vaccine candidates against Shigella sonnei are under clinical development, including a Generalized Modules for Membrane Antigens (GMMA)-based vaccine. The mechanisms by which GMMA-based vaccines interact and activate human immune cells remain elusive. Our previous study provided the first evidence that both adaptive and innate immune cells are targeted and functionally shaped by the GMMA-based vaccine. Here, flow cytometry and confocal microscopy analysis allowed us to identify monocytes as the main target population interacting with the S. sonnei 1790-GMMA vaccine on human peripheral blood. In addition, transcriptomic analysis of this cell population revealed a molecular signature induced by 1790-GMMA mostly correlated with the inflammatory response and cytokine-induced processes. This also impacts the expression of genes associated with macrophages’ differentiation and T cell regulation, suggesting a dual function for this vaccine platform both as an antigen carrier and as a regulator of immune cell activation and differentiation.
Funder
GlaxoSmithKline Biologicals SA GSK
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