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Fibrinogen\u2010like protein\u20102 (<jats:styled-content style=\"fixed-case\">FGL<\/jats:styled-content>2) is a potent effector molecule of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup>\u00a0<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>25<jats:sup>+<\/jats:sup>\u00a0FoxP3<jats:sup>+<\/jats:sup> regulatory T cells and exerts its immunosuppressive activity following ligation to its cognate receptor, Fc<jats:italic>\u03b3<\/jats:italic><jats:styled-content style=\"fixed-case\">RIIB<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">RIII<\/jats:styled-content>. The role of <jats:styled-content style=\"fixed-case\">FGL<\/jats:styled-content>2 in the pathogenesis of chronic viral infection caused by lymphocytic choriomeningitis virus clone\u201013 (<jats:styled-content style=\"fixed-case\">LCMV<\/jats:styled-content> cl\u201013) was assessed in this study. Chronically infected <jats:italic>fgl2<\/jats:italic><jats:sup>+\/+<\/jats:sup> mice had increased plasma levels of <jats:styled-content style=\"fixed-case\">FGL<\/jats:styled-content>2, with reduced expression of the maturation markers, <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>80, <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>86 and <jats:styled-content style=\"fixed-case\">MHC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">II<\/jats:styled-content> on macrophages and dendritic cells and impaired production of neutralizing antibody. In contrast, <jats:italic>fgl2<\/jats:italic><jats:sup><jats:italic>\u2212\/\u2212<\/jats:italic><\/jats:sup> mice or <jats:italic>fgl2<\/jats:italic><jats:sup><jats:italic>+\/+<\/jats:italic><\/jats:sup> mice that had been pre\u2010treated with antibodies to <jats:styled-content style=\"fixed-case\">FGL<\/jats:styled-content>2 and Fc<jats:italic>\u03b3<\/jats:italic><jats:styled-content style=\"fixed-case\">RIIB<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">RIII<\/jats:styled-content> and then infected with <jats:styled-content style=\"fixed-case\">LCMV<\/jats:styled-content> cl\u201013 developed a robust <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> antiviral T\u2010cell response, produced high titred neutralizing antibody to <jats:styled-content style=\"fixed-case\">LCMV<\/jats:styled-content> and cleared <jats:styled-content style=\"fixed-case\">LCMV<\/jats:styled-content>. Treatment of mice with established chronic infection with antibodies to <jats:styled-content style=\"fixed-case\">FGL<\/jats:styled-content>2 and Fc<jats:italic>\u03b3<\/jats:italic><jats:styled-content style=\"fixed-case\">RIIB<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">RIII<\/jats:styled-content> was shown to rescue the number and functionality of virus\u2010specific <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> T cells with reduced total and virus\u2010specific T\u2010cell expression of programmed cell death protein 1 leading to viral clearance. These results demonstrate an important role for <jats:styled-content style=\"fixed-case\">FGL<\/jats:styled-content>2 in viral immune evasion and provide a rationale to target <jats:styled-content style=\"fixed-case\">FGL<\/jats:styled-content>2 to treat patients with chronic viral infection.<\/jats:p>","DOI":"10.1111\/imm.12897","type":"journal-article","created":{"date-parts":[[2018,1,17]],"date-time":"2018-01-17T13:32:34Z","timestamp":1516195954000},"page":"476-489","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":15,"title":["Inhibition of the Fibrinogen\u2010Like Protein 2:Fc<i>\u03b3<\/i><scp>RIIB<\/scp>\/<scp>RIII<\/scp> immunosuppressive pathway enhances antiviral T\u2010cell and B\u2010cell responses leading to clearance of lymphocytic choriomeningitis virus clone 13"],"prefix":"10.1111","volume":"154","author":[{"given":"Olga","family":"Luft","sequence":"first","affiliation":[{"name":"Toronto General Hospital Multi 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