Indoleamine 2,3-dioxygenase activity as a potential biomarker of immune suppression during visceral leishmaniasis

Innate Immun. 2013 Dec;19(6):564-8. doi: 10.1177/1753425912473170. Epub 2013 Feb 14.

Abstract

Leishmania parasites induce an immunomodulation by subverting the host immune response towards a CD4(+) Th2 lymphocytic cell response that favors parasite persistence. Here, we report that after successful treatment of visceral leishmaniasis due to Leishmania infantum, an immune reconstitution syndrome revealing hip septic arthritis was associated with a switch from Th2 towards a Th1 cytokine profile, and a decrease in the level of immunomodulating factors, such as soluble HLA-G and indoleamine 2,3-dioxygenase (IDO) activity. We then measured IDO activity in a cohort of 39 patients and uninfected control subjects. Results showed significantly enhanced IDO activity in patients with visceral Leishmania infection, compared with uninfected control subjects (P < 0.001), but also compared with treated patients (P < 0.05). A decrease in IDO activity could constitute a relevant biomarker for the restoration of the immune response during visceral leishmaniasis.

Keywords: 3-dioxygenase; HLA-G; Indoleamine 2; Leishmania; immune reconstitution syndrome; immune response; visceral leishmaniasis.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Arthritis, Infectious / diagnosis*
  • Arthritis, Infectious / etiology
  • Arthritis, Infectious / immunology*
  • Biomarkers / blood*
  • Child
  • Child, Preschool
  • Cytokines / blood
  • Female
  • HLA-G Antigens / blood
  • Hip / microbiology
  • Hip / pathology
  • Humans
  • Immune Evasion
  • Immunologic Tests
  • Immunosuppression Therapy
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / blood*
  • Infant
  • Leishmania infantum / immunology*
  • Leishmaniasis, Visceral / complications
  • Leishmaniasis, Visceral / diagnosis*
  • Leishmaniasis, Visceral / immunology*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Th1-Th2 Balance
  • Th2 Cells / immunology*
  • Th2 Cells / microbiology
  • Young Adult

Substances

  • Biomarkers
  • Cytokines
  • HLA-G Antigens
  • Indoleamine-Pyrrole 2,3,-Dioxygenase