%0 Journal Article %J Front Immunol %D 2018 %T Allergic Asthma Favors Growth in the Lungs of Infected Mice. %A Arnaud Machelart %A Potemberg, Georges %A Laurye Van Maele %A Aurore Demars %A Maxime Lagneaux %A Carl De Trez %A Catherine Sabatel %A Bureau, Fabrice %A De Prins, Sofie %A Pauline Percier %A Olivier J Denis %A Fabienne Jurion %A Marta Romano %A Vanderwinden, Jean-Marie %A Letesson, Jean-Jacques %A Eric Muraille %K allergic asthma %K Brucella melitensis %K Brucellosis %K INFECTION %K Mycobacterium tuberculosis %K Streptococcus pneumoniae %X

Allergic asthma is a chronic Th2 inflammatory disease of the lower airways affecting a growing number of people worldwide. The impact of infections and microbiota composition on allergic asthma has been investigated frequently. Until now, however, there have been few attempts to investigate the impact of asthma on the control of infectious microorganisms and the underlying mechanisms. In this work, we characterize the consequences of allergic asthma on intranasal (i.n.) infection by bacteria in mice. We observed that i.n. sensitization with extracts of the house dust mite or the mold () significantly increased the number of , and in the lungs of infected mice. Microscopic analysis showed dense aggregates of infected cells composed mainly of alveolar macrophages (CD11c F4/80 MHCII) surrounded by neutrophils (Ly-6G). Asthma-induced susceptibility appears to be dependent on CD4 T cells, the IL-4/STAT6 signaling pathway and IL-10, and is maintained in IL-12- and IFN-γR-deficient mice. The effects of the sensitization protocol were also tested on and pulmonary infections. Surprisingly, we observed that sensitization strongly increases the survival of infected mice by a T cell and STAT6 independent signaling pathway. In contrast, the course of infection is not affected in the lungs of sensitized mice. Our work demonstrates that the impact of the same allergic sensitization protocol can be neutral, negative, or positive with regard to the resistance of mice to bacterial infection, depending on the bacterial species.

%B Front Immunol %V 9 %8 2018 %G eng %R 10.3389/fimmu.2018.01856