Concanavalin-A displays leishmanicidal activity by inducing ROS production in human peripheral blood mononuclear cells

Immunopharmacol Immunotoxicol. 2018 Oct;40(5):387-392. doi: 10.1080/08923973.2018.1510960. Epub 2018 Sep 5.

Abstract

The context of the article: Leishmania amazonensis has a wide geographical distribution throughout South American countries and can cause self-healing to severe cases as mucocutaneous or visceral forms. Leishmaniasis presents a balance of inflammatory and anti-inflammatory cytokines which is responsible for promoting the activation of phagocytes, essential to control the infection and lead to tissue repair/resolution of the disease, respectively. Results and discussion: Our model revealed that the treatment with Con-A was capable to stimulate human PBMC cells by increasing the phagocytic capacity and promoting parasite elimination. The pretreatment with Con-A promoted inflammatory (IFN-γ, TNF-α, IL-2 and IL-6) and anti-inflammatory (IL-4 and IL-10) cytokines production, increased the reactive oxygen species (ROS) sinthesys as well as the expression and presence of iNOS enzyme, but not nitric oxide production. Conclusion: Based on the data obtained, it was possible to infer that Con-A induces the ROS production, responsible for eliminating parasites in addition to regulatory cytokines synthesis which are important for disease resolution.

Keywords: Con-A; Leishmania amazonensis; PBMC; cytokine; iNOS; reactive oxygen species.

MeSH terms

  • Animals
  • Antiprotozoal Agents / pharmacology*
  • Cells, Cultured
  • Concanavalin A / pharmacology*
  • Cytokines / biosynthesis
  • Healthy Volunteers
  • Humans
  • Immunity, Cellular / drug effects
  • Leishmania / drug effects*
  • Leukocytes, Mononuclear / drug effects*
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Leukocytes, Mononuclear / parasitology
  • Nitric Oxide Synthase Type II / genetics
  • Phagocytes / drug effects
  • Phagocytes / immunology
  • Phagocytes / metabolism
  • Phagocytes / parasitology
  • Reactive Oxygen Species / metabolism*

Substances

  • Antiprotozoal Agents
  • Cytokines
  • Reactive Oxygen Species
  • Concanavalin A
  • NOS2 protein, human
  • Nitric Oxide Synthase Type II