Myeloid cell TNFR1 signaling dependent liver injury and inflammation upon BCG infection

Leslie Chavez-Galan , Dominique Vesin , Guillaume Blaser , Husnu Uysal , Sulayman Benmerzoug (1) , Stéphanie Rose (1) , Bernhard Ryffel (1) , Valérie Quesniaux (1) , Irène Garcia (2)

1 INEM - Immunologie et Neurogénétique Expérimentales et Moléculaires
2 UNIGE - Université de Genève = University of Geneva

TNF plays a critical role in mononuclear cell recruitment during acute Bacillus Calmette-Guérin (BCG) infection leading to an effective immune response with granuloma formation, but may also cause tissue injury mediated by TNFR1 or TNFR2. Here we investigated the role of myeloid and T cell specific TNFR1 and R2 expression, and show that absence of TNFR1 in myeloid cells attenuated liver granuloma formation and liver injury in response to acute BCG infection, while TNFR2 expressed in myeloid cells contributed only to liver injury. TNFR1 was the main receptor controlling cytokine production by liver mononuclear cells after antigenic specific response, modified CD4/CD8 ratio and NK, NKT and regulatory T cell recruitment. Further analysis of CD11b + CD3 + phagocytic cells revealed a TCRαβ expressing subpopulation of unknown function, which increased in response to BCG infection dependent of TNFR1 expression on myeloid cells. In conclusion, TNFR1 expressed by myeloid cells plays a critical role in mononuclear cell recruitment and injury of the liver after BCG infection.

Domains: Life Sciences [q-bio]; Life Sciences [q-bio]; Immunology

Leslie Chavez-Galan, Dominique Vesin, Guillaume Blaser, Husnu Uysal, Sulayman Benmerzoug, et al.. Myeloid cell TNFR1 signaling dependent liver injury and inflammation upon BCG infection. Scientific Reports, 2019, 9 (1), ⟨10.1038/s41598-019-41629-9⟩. ⟨hal-02126394⟩