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Integrated analysis of whole blood oxylipin and cytokine responses after bacterial, viral, and T cell stimulation reveals new immune networks

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Villain, Etienne | Chanson, Aurélie | Mainka, Malwina | Kampschulte, Nadja | Le Faouder, Pauline | Bertrand-Michel, Justine | Brandolini, Marion | Charbit, Bruno | Musvosvi, Munyaradzi | Bilek, Nicole | Scriba, Thomas | Quintana-Murci, Lluis | Schebb, Nils Helge | Duffy, Darragh | Gladine, Cécile | Abel, Laurent | Alcover, Andrés | Aschard, Hugues | Bousso, Philippe | Bourke, Nollaig | Brodin, Petter | Bruhns, Pierre | Cerf-Bensussan, Nadine | Cumano, Ana | D’enfert, Christophe | Deriano, Ludovic | Dillies, Marie-Agnès | Di Santo, James | Eberl, Gérard | Enninga, Jost | Fellay, Jacques | Gomperts-Boneca, Ivo | Hasan, Milena | Hedestam, Gunilla Karlsson | Hercberg, Serge | Ingersoll, Molly | Lantz, Olivier | Kenny, Rose Anne | Ménager, Mickaël | Mouquet, Hugo | O'Farrelly, Cliona | Patin, Etienne | Pellegrini, Sandra | Rausell, Antonio | Rieux-Laucat, Frédéric | Rogge, Lars | Fontes, Magnus | Sakuntabhai, Anavaj | Schwartz, Olivier | Schwikowski, Benno | Shorte, Spencer | Tangy, Frédéric | Toubert, Antoine | Touvier, Mathilde | Ungeheuer, Marie-Noëlle | Zimmer, Christophe | Albert, Matthew

Edité par CCSD ; Elsevier -

International audience. Oxylipins are major immunomodulating mediators, yet studies of inflammation focus mainly on cytokines. Here, using a standardized whole-blood stimulation system, we characterized the oxylipin-driven inflammatory responses to various stimuli and their relationships with cytokine responses. We performed a pilot study in 25 healthy individuals using 6 different stimuli: 2 bacterial stimuli (LPS and live BCG), 2 viral stimuli (vaccine-grade poly I:C and live H1N1 attenuated influenza), an enterotoxin superantigen and a Null control. All stimuli induced a strong production of oxylipins but most importantly, bacterial, viral, and T cell immune responses show distinct oxylipin signatures. Integration of the oxylipin and cytokine responses for each condition revealed new immune networks improving our understanding of inflammation regulation. Finally, the oxylipin responses and oxylipin-cytokine networks were compared in patients with active tuberculosis or with latent infection. This revealed different responses to BCG but not LPS stimulation highlighting new regulatory pathways for further investigations.

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