Literature DB >> 31484831

Progranulin prevents regulatory NK cell cytotoxicity against antiviral T cells.

Anfei Huang1, Prashant V Shinde1, Jun Huang1, Tina Senff2, Haifeng C Xu1, Cassandra Margotta1, Dieter Häussinger3, Thomas E Willnow4, Jinping Zhang5, Aleksandra A Pandyra1,3, Jörg Timm2, Sascha Weggen6, Karl S Lang7, Philipp A Lang1.   

Abstract

`NK cell-mediated regulation of antigen-specific T cells can contribute to and exacerbate chronic viral infection, but the protective mechanisms against NK cell-mediated attack on T cell immunity are poorly understood. Here, we show that progranulin (PGRN) can reduce NK cell cytotoxicity through reduction of NK cell expansion, granzyme B transcription, and NK cell-mediated lysis of target cells. Following infection with the lymphocytic choriomeningitis virus (LCMV), PGRN levels increased - a phenomenon dependent on the presence of macrophages and type I IFN signaling. Absence of PGRN in mice (Grn-/-) resulted in enhanced NK cell activity, increased NK cell-mediated killing of antiviral T cells, reduced antiviral T cell immunity, and increased viral burden, culminating in increased liver immunopathology. Depletion of NK cells restored antiviral immunity and alleviated pathology during infection in Grn-/- mice. In turn, PGRN treatment improved antiviral T cell immunity. Taken together, we identified PGRN as a critical factor capable of reducing NK cell-mediated attack of antiviral T cells.

Entities:  

Keywords:  Adaptive immunity; Immunology; Infectious disease; Innate immunity; NK cells

Mesh:

Substances:

Year:  2019        PMID: 31484831      PMCID: PMC6777906          DOI: 10.1172/jci.insight.129856

Source DB:  PubMed          Journal:  JCI Insight        ISSN: 2379-3708


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