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10.3389/fimmu.2017.00178

http://scihub22266oqcxt.onion/10.3389/fimmu.2017.00178
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C5318425!5318425!28270815
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suck abstract from ncbi


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pmid28270815      Front+Immunol 2017 ; 8 (ä): ä
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  • Lanthionine Synthetase C-Like 2 Modulates Immune Responses to Influenza Virus Infection #MMPMID28270815
  • Leber A; Bassaganya-Riera J; Tubau-Juni N; Zoccoli-Rodriguez V; Lu P; Godfrey V; Kale S; Hontecillas R
  • Front Immunol 2017[]; 8 (ä): ä PMID28270815show ga
  • Broad-based, host-targeted therapeutics have the potential to ameliorate viral infections without inducing antiviral resistance. We identified lanthionine synthetase C-like 2 (LANCL2) as a new therapeutic target for immunoinflammatory diseases. To examine the therapeutic efficacy of oral NSC61610 administration on influenza, we infected C57BL/6 mice with influenza A H1N1pdm virus and evaluated influenza-related mortality, lung inflammatory profiles, and pulmonary histopathology. Oral treatment with NSC61610 ameliorates influenza virus infection by down-modulating pulmonary inflammation through the downregulation of TNF-? and MCP-1 and reduction in the infiltration of neutrophils. NSC61610 treatment increases IL10-producing CD8+ T cells and macrophages in the lungs during the resolution phase of disease. The loss of LANCL2 or neutralization of IL-10 in mice infected with influenza virus abrogates the ability of NSC61610 to accelerate recovery and induce IL-10-mediated regulatory responses. These studies validate that oral treatment with NSC61610 ameliorates morbidity and mortality and accelerates recovery during influenza virus infection through a mechanism mediated by activation of LANCL2 and subsequent induction of IL-10 responses by CD8+ T cells and macrophages in the lungs.
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