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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
Author(s) -
Edith A. Fernández-Figueroa,
Iván Imaz-Rosshandler,
Juan CastilloFernandez,
Haydee Miranda-Ortíz,
Juan Carlos Fernández-López,
Ingeborg Becker,
Claudia RangelEscareño
Publication year - 2016
Publication title -
plos neglected tropical diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.99
H-Index - 135
eISSN - 1935-2735
pISSN - 1935-2727
DOI - 10.1371/journal.pntd.0004570
Subject(s) - cutaneous leishmaniasis , lipophosphoglycan , leishmaniasis , leishmania , leishmania mexicana , immunology , biology , tlr2 , leishmania major , innate immune system , immune system , jak stat signaling pathway , stat , effector , signal transduction , leishmania donovani , microbiology and biotechnology , visceral leishmaniasis , stat3 , parasite hosting , tyrosine kinase , world wide web , computer science
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.

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