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Mucosal Immunol ; 6(5): 931-41, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23250274

ABSTRACT

Co-infection with mycobacteria and helminths is widespread in developing countries, but how this alters host immunological control of each pathogen is not comprehensively understood. In this study, we demonstrate that acute Nippostrongylus brasiliensis (Nb) murine infection reduce early pulmonary mycobacterial colonization. This Nb-associated reduction in pulmonary Mycobacterium tuberculosis colony-forming units was associated with early and increased activation of pulmonary CD4 T cells and increased T helper type 1 (Th1) and Th2 cytokine secretion. An accelerated and transient augmentation of neutrophils and alveolar macrophages (AMs) was also observed in co-infected animals. AMs displayed markers of both classical and alternative activation. Intranasal transfer of pulmonary macrophages obtained from donor mice 5 days after Nb infection significantly reduced pulmonary Mycobacterium bovis Bacille Calmette-Guérin clearance in recipient mice. These data demonstrate that early stage Nb infection elicits a macrophage response, which is protective during the early stages of subsequent mycobacterial infection.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , Coinfection/immunology , Macrophages, Alveolar/immunology , Mycobacterium tuberculosis/immunology , Nippostrongylus/immunology , Strongylida Infections/immunology , Tuberculosis, Pulmonary/immunology , Acute Disease , Adoptive Transfer , Animals , Bacterial Load , Cells, Cultured , Cytokines/metabolism , Female , Lung/immunology , Lymphocyte Activation , Macrophage Activation , Macrophages, Alveolar/transplantation , Mice , Mice, Inbred BALB C , Th1-Th2 Balance
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