Inhibition of MHC-I by Brucella abortus is an early event during infection and involves EGFR pathway

VELASQUEZ, LIS N.(PRIMERA AUTORA); MILILLO, M. AYELÉN (PRIMERA AUTORA); DELPINO, VICTORIA; TROTTA, ALDANA; MERCOGLIANO, MF; POZNER, ROBERTO G.; SCHILLACI, ROXANA; ELIZALDE, PATRICIA V.; GIAMBARTOLOMEI, GUILLERMO; BARRIONUEVO, PAULA; *AMBAS AUTORAS CONTRIBUYERON DE MANERA EQUIVALENTE AL TRABAJO

IMMUNOLOGY AND CELL BIOLOGY

NATURE PUBLISHING GROUP

Lugar: Londres; Año: 2017 vol. 95 p. 388 - 398

0818-9641

Brucella abortus is able to persist inside the host despite the development of potent CD8+ T cell responses. We have recently reported the ability of B. abortus to inhibit the IFN-γ-induced MHC-I cell surface expression on human monocytes. This phenomenon was due to the B. abortus-mediated retention of MHC-I molecules within the Golgi apparatus and was dependent on bacterial viability. However, the implications of bacterial virulence or replicative capacity and the signaling pathways remained unknown. Here, we demonstrated that the B. abortus mutant strains RB51 and virB10- are able to inhibit MHC-I expression in the same manner as wild type B. abortus, even though they are unable to persist inside human monocytes for a long period of time. Consistent with this, the phenomenon was triggered early in time and could be observed at 8 h post-infection. At 24 h and 48 h it was even stronger. Regarding the signaling pathway, targeting EGF receptor (EGFR), ErbB2 (HER2) or inhibition of TACE, one of the enzymes which generates soluble EGF-like ligands, resulted in partial recovery of MHC-I surface expression. Moreover, recombinant EGF and TGF-α as well as the combination of both were also able to reproduce the B. abortus-induced MHC-I down-modulation. Finally, when infection was performed in the presence of an Erk1/2 inhibitor, MHC-I surface expression was significantly recovered. Overall, these results describe how B. abortus evades CD8+ T cell responses early during infection and exploits the EGFR-ERK signaling pathway to escape from the immune system and favor chronicity.