Monocyte subpopulations as important biomarkers of resistence and susceptibility during experimental infection with Leishmania (Leishmania) major

Biomed Pharmacother. 2018 Nov:107:1530-1539. doi: 10.1016/j.biopha.2018.08.154. Epub 2018 Sep 5.

Abstract

Visceral Leishmaniasis is a chronic and lethal, parasitic disease. In the later infection stages, it is known that expressive hematological disorders can be observed, including changes in the frequency and phenotype of certain leukocytes. There is a lack of good prognostic indicators to characterize the on-goin clinical status of the patient. In this study, we have analyzed the frequency of monocyte subpopulations in mice infected with Leishmania major (L. major). Our results show a significant correlation between increased blood monocyte frequency and lesion development in both BALB/c and in the C57BL/6 mice infected with L. major. In BALB/c mice we observed a significant correlation between the frequency of GR1+ monocytes and lesion size. Furthermore, treatment of infected BALB/c mice with Anfotericin B, to resolve lesions, resulted in a lower frequency of GR1+ monocytes compared to untreated infected BALB/c mice. C57BL/6 infected mice, which normally resolve infections, show decreased numbers of monocytes during the healing phase of infection. The results indicate that disease severity can be predicted by analyzing monocyte frequency. Thus, we propose that the frequency of monocytes, can be used to define the severity of the disease as well as the success of the treatment in experimental leishmaniasis.

Keywords: Biomarkers; Leishmania; Monocyte subpopulation; Resistance; Susceptibility.

MeSH terms

  • Amphotericin B / pharmacology*
  • Animals
  • Antiprotozoal Agents / pharmacology
  • Biomarkers
  • Disease Models, Animal
  • Female
  • Leishmania major / drug effects
  • Leishmania major / isolation & purification*
  • Leishmaniasis, Visceral / drug therapy
  • Leishmaniasis, Visceral / parasitology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Monocytes / metabolism
  • Monocytes / parasitology*
  • Severity of Illness Index

Substances

  • Antiprotozoal Agents
  • Biomarkers
  • Amphotericin B