IL-6 is required for protective immune responses against early filarial infection

Int J Parasitol. 2018 Oct;48(12):925-935. doi: 10.1016/j.ijpara.2018.05.011. Epub 2018 Sep 1.

Abstract

IL-6 has a wide range of biological activities that includes anti- and pro-inflammatory aspects. In this study, we investigated the role of IL-6 in immune responses to the rodent filarial nematode Litomosoides sigmodontis, a model for human filarial infections. IL-6-/- mice had a significantly increased worm burden after natural infection compared with wild type controls at early time points p.i. Given that the worm burden in IL-6-/- mice was already increased at the time point the infective larvae reached the pleural cavity, immune responses that may facilitate the migration from the site of infection (skin) via the lymphatics to the pleural cavity were analysed. Increased vascular permeability may facilitate larval migration, but blocking of histamine receptors had no effect on worm burden and vascular permeability was similar between IL-6-/- mice and wild type controls. In contrast, blocking mast cell degranulation reduced the worm burden in IL-6-/- mice partially, suggesting that release of mast cell-derived mediators improves larval migration to some degree. Protective immune responses within the skin were involved, as bypassing the skin barrier by inoculating infective L3s subcutaneously resulted in a comparable worm recovery in both mouse strains. Analysis of the cellular composition by flow cytometry and PCR array in the skin after exposure to filarial extract or L3s, respectively, indicate that the absence of IL-6 results in a delayed recruitment of neutrophils and macrophages to the site of initial infection. These results demonstrate that IL-6 is essentially involved in protective immune responses within the skin that impair migration of infective L3s.

Keywords: Filaria; Helminth; Histamine; IL-6; L3 larva; Litomosoides sigmodontis; Neutrophil; Skin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement
  • Disease Models, Animal
  • Filariasis / immunology*
  • Filariasis / parasitology
  • Filarioidea / immunology*
  • Filarioidea / physiology
  • Interleukin-6 / deficiency
  • Interleukin-6 / metabolism*
  • Macrophages / immunology
  • Mast Cells / immunology
  • Mice
  • Neutrophils / immunology
  • Pleural Cavity / parasitology
  • Skin / immunology
  • Skin / parasitology

Substances

  • Interleukin-6
  • interleukin-6, mouse