Mouse cytomegalovirus-experienced ILC1s acquire a memory response dependent on the viral glycoprotein m12.

Abstract:

:Innate lymphoid cells (ILCs) are tissue-resident sentinels that are essential for early host protection from pathogens at initial sites of infection. However, whether pathogen-derived antigens directly modulate the responses of tissue-resident ILCs has remained unclear. In the present study, it was found that liver-resident type 1 ILCs (ILC1s) expanded locally and persisted after the resolution of infection with mouse cytomegalovirus (MCMV). ILC1s acquired stable transcriptional, epigenetic and phenotypic changes a month after the resolution of MCMV infection, and showed an enhanced protective effector response to secondary challenge with MCMV consistent with a memory lymphocyte response. Memory ILC1 responses were dependent on the MCMV-encoded glycoprotein m12, and were independent of bystander activation by proinflammatory cytokines after heterologous infection. Thus, liver ILC1s acquire adaptive features in an MCMV-specific manner.

journal_name

Nat Immunol

journal_title

Nature immunology

authors

Weizman OE,Song E,Adams NM,Hildreth AD,Riggan L,Krishna C,Aguilar OA,Leslie CS,Carlyle JR,Sun JC,O'Sullivan TE

doi

10.1038/s41590-019-0430-1

subject

Has Abstract

pub_date

2019-08-01 00:00:00

pages

1004-1011

issue

8

eissn

1529-2908

issn

1529-2916

pii

10.1038/s41590-019-0430-1

journal_volume

20

pub_type

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