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Int J Parasitol ; 47(1): 1-10, 2017 01.
Article in English | MEDLINE | ID: mdl-28003150

ABSTRACT

The aim of this work was to elucidate the immunopathological mechanisms of how helminths may influence the course of a viral infection, using a murine model. Severe virulence, a relevant increase in the virus titres in the lung and a higher mortality rate were observed in Ascaris and Vaccinia virus (VACV) co-infected mice, compared with VACV mono-infected mice. Immunopathological analysis suggested that the ablation of CD8+ T cells, the marked reduction of circulating CD4+ T cells producing IFN-γ, and the robust pulmonary inflammation were associated with the increase of morbidity/mortality in co-infection and subsequently with the negative impact of concomitant pulmonary ascariasis and respiratory VACV infection for the host. On the other hand, when evaluating the impact of the co-infection on the parasitic burden, co-infected mice presented a marked decrease in the total number of migrating Ascaris lung-stage larvae in comparison with Ascaris mono-infection. Taken together, our major findings suggest that Ascaris and VACV co-infection may potentiate the virus-associated pathology by the downmodulation of the VACV-specific immune response. Moreover, this study provides new evidence of how helminth parasites may influence the course of a coincident viral infection.


Subject(s)
Ascariasis/virology , Ascaris/immunology , Coinfection/immunology , Pneumonia/parasitology , Vaccinia virus/immunology , Vaccinia/etiology , Animals , Ascariasis/immunology , CD8-Positive T-Lymphocytes/immunology , Coinfection/parasitology , Coinfection/virology , Cytokines/immunology , Disease Models, Animal , Female , Interferon-gamma/immunology , Larva/parasitology , Lung/immunology , Lung/parasitology , Lung/pathology , Lung/virology , Mice , Mice, Inbred BALB C , Pneumonia/immunology , Pneumonia/virology , Swine , Vaccinia/immunology , Vaccinia/pathology , Vaccinia/virology , Viral Load
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