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10.1038/srep46363

http://scihub22266oqcxt.onion/10.1038/srep46363
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C5385529!5385529!28393908
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suck abstract from ncbi


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pmid28393908      Sci+Rep 2017 ; 7 (ä): ä
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  • Resolvin D1 drives establishment of Leishmania amazonensis infection #MMPMID28393908
  • Malta-Santos H; Andrade BB; Zanette DL; Costa JM; Bozza PT; Bandeira-Melo C; Barral A; França-Costa J; Borges VM
  • Sci Rep 2017[]; 7 (ä): ä PMID28393908show ga
  • Previous studies have indicated that the balance between different eicosanoids reflect the intensity of the inflammatory profile in patients with tegumentary leishmaniasis. More recently, pro-resolution lipid mediators have been shown to play critical roles in dampening pathological inflammatory processes to reestablish homeostasis in a diverse range of experimental settings. Among these lipid mediator, resolvins from D series have been described as potent anti-inflammatory and immunomodulatory mediators, and its activities include inhibition of leukocyte chemotaxis and blockage production of proinflammatory cytokines, while increasing the expression of regulatory mediators. Whether resolvins play significant roles in establishment and persistence of Leishmania infection is currently unknown. We addressed this question in the current study by assessing circulating levels of D-series resolvins in tegumentary leishmaniasis patients presenting with localized or diffuse disease. We found heightened expression of resolvin D1 in diffuse cutaneous leishmaniasis which was correlated with expression profile of biomarkers associated with disease pathogenesis. Additional in vitro experiments using primary human macrophages indicated that resolvin D1 may promote intracellular Leishmania amazonensis replication through a mechanism associated with induction of heme oxygenase-1. These results suggest that targeting resolvin D1 could serve as potential strategy for host directed therapy in diffuse cutaneous leishmaniasis.
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