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10.1172/jci.insight.83116

http://scihub22266oqcxt.onion/10.1172/jci.insight.83116
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C4855513!4855513!27158671
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suck abstract from ncbi


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pmid27158671      JCI+Insight ä ; 1 (4): ä
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  • Vaccinia vaccine?based immunotherapy arrests and reverses established pulmonary fibrosis #MMPMID27158671
  • Collins SL; Chan-Li Y; Oh M; Vigeland CL; Limjunyawong N; Mitzner W; Powell JD; Horton MR
  • JCI Insight ä[]; 1 (4): ä PMID27158671show ga
  • Idiopathic pulmonary fibrosis (IPF) is a fatal disease without any cure. Both human disease and animal models demonstrate dysregulated wound healing and unregulated fibrogenesis in a background of low-grade chronic T lymphocyte infiltration. Tissue-resident memory T cells (Trm) are emerging as important regulators of the immune microenvironment in response to pathogens, and we hypothesized that they might play a role in regulating the unremitting inflammation that promotes lung fibrosis. Herein, we demonstrate that lung-directed immunotherapy, in the form of i.n. vaccination, induces an antifibrotic T cell response capable of arresting and reversing lung fibrosis. In mice with established lung fibrosis, lung-specific T cell responses were able to reverse established pathology ? as measured by decreased lung collagen, fibrocytes, and histologic injury ? and improve physiologic function. Mechanistically, we demonstrate that this effect is mediated by vaccine-induced lung Trm. These data not only have implications for the development of immunotherapeutic regimens to treat IPF, but also suggest a role for targeting tissue-resident memory T cells to treat other tissue-specific inflammatory/autoimmune disorders.
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