Down-Regulation of TLR and JAK/STAT Pathway Genes Is Associated with Diffuse Cutaneous Leishmaniasis: A Gene Expression Analysis in NK Cells from Patients Infected with Leishmania mexicana

PLoS Negl Trop Dis. 2016 Mar 31;10(3):e0004570. doi: 10.1371/journal.pntd.0004570. eCollection 2016 Mar.

Abstract

An important NK-cell inhibition with reduced TNF-α, IFN-γ and TLR2 expression had previously been identified in patients with diffuse cutaneous leishmaniasis (DCL) infected with Leishmania mexicana. In an attempt to pinpoint alterations in the signaling pathways responsible for the NK-cell dysfunction in patients with DCL, this study aimed at identifying differences in the NK-cell response towards Leishmania mexicana lipophosphoglycan (LPG) between patients with localized and diffuse cutaneous leishmaniasis through gene expression profiling. Our results indicate that important genes involved in the innate immune response to Leishmania are down-regulated in NK cells from DCL patients, particularly TLR and JAK/STAT signaling pathways. This down-regulation showed to be independent of LPG stimulation. The study sheds new light for understanding the mechanisms that undermine the correct effector functions of NK cells in patients with diffuse cutaneous leishmaniasis contributing to a better understanding of the pathobiology of leishmaniasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Down-Regulation
  • Gene Expression Regulation / physiology
  • Humans
  • Janus Kinases / genetics
  • Janus Kinases / metabolism*
  • Killer Cells, Natural / physiology*
  • Leishmania mexicana*
  • Leishmaniasis, Diffuse Cutaneous / metabolism*
  • STAT Transcription Factors / genetics
  • STAT Transcription Factors / metabolism*
  • Signal Transduction / physiology
  • Toll-Like Receptors / metabolism*
  • Transcriptome

Substances

  • STAT Transcription Factors
  • Toll-Like Receptors
  • Janus Kinases

Grants and funding

The work was funded by INMEGEN 144 2013-06-26, INMEGEN 33 2008-06-01, PAPIIT IN217515, CONACyT 221405 and FINNOVA-CONACyT 242368. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.