Fate mapping of single NK cells identifies a type 1 innate lymphoid-like lineage that bridges innate and adaptive recognition of viral infection.


Journal

Immunity
ISSN: 1097-4180
Titre abrégé: Immunity
Pays: United States
ID NLM: 9432918

Informations de publication

Date de publication:
12 10 2021
Historique:
received: 24 12 2020
revised: 21 05 2021
accepted: 03 08 2021
pubmed: 27 8 2021
medline: 10 11 2021
entrez: 26 8 2021
Statut: ppublish

Résumé

Upon viral infection, natural killer (NK) cells expressing certain germline-encoded receptors are selected, expanded, and maintained in an adaptive-like manner. Currently, these are thought to differentiate along a common pathway. However, by fate mapping of single NK cells upon murine cytomegalovirus (MCMV) infection, we identified two distinct NK cell lineages that contributed to adaptive-like responses. One was equivalent to conventional NK (cNK) cells while the other was transcriptionally similar to type 1 innate lymphoid cells (ILC1s). ILC1-like NK cells showed splenic residency and strong cytokine production but also recognized and killed MCMV-infected cells, guided by activating receptor Ly49H. Moreover, they induced clustering of conventional type 1 dendritic cells and facilitated antigen-specific T cell priming early during MCMV infection, which depended on Ly49H and the NK cell-intrinsic expression of transcription factor Batf3. Thereby, ILC1-like NK cells bridge innate and adaptive viral recognition and unite critical features of cNK cells and ILC1s.

Identifiants

pubmed: 34437840
pii: S1074-7613(21)00332-0
doi: 10.1016/j.immuni.2021.08.002
pmc: PMC8528403
mid: EMS135905
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2288-2304.e7

Subventions

Organisme : European Research Council
ID : 949719
Pays : International
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

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Auteurs

Sophie Flommersfeld (S)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.

Jan P Böttcher (JP)

Institute of Molecular Immunology and Experimental Oncology, Klinikum Rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.

Jonatan Ersching (J)

Laboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY 10065, USA.

Michael Flossdorf (M)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.

Philippa Meiser (P)

Institute of Molecular Immunology and Experimental Oncology, Klinikum Rechts der Isar, School of Medicine, Technical University of Munich (TUM), Munich, Germany.

Ludwig O Pachmayr (LO)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.

Justin Leube (J)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.

Inge Hensel (I)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.

Sebastian Jarosch (S)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.

Qin Zhang (Q)

Division of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany; BioQuant Center, University of Heidelberg, Heidelberg, Germany.

M Zeeshan Chaudhry (MZ)

Helmholtz Centre for Infection Research, Braunschweig, Germany.

Immanuel Andrae (I)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.

Matthias Schiemann (M)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany.

Dirk H Busch (DH)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany; German Center for Infection Research (DZIF), Partner Site Munich, Munich, Germany.

Luka Cicin-Sain (L)

Helmholtz Centre for Infection Research, Braunschweig, Germany.

Joseph C Sun (JC)

Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Georg Gasteiger (G)

Würzburg Institute of Systems Immunology, Würzburg, Germany; Max Planck Research Group at the Julius-Maximilians-Universität Würzburg, Würzburg, Germany.

Gabriel D Victora (GD)

Laboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY 10065, USA.

Thomas Höfer (T)

Division of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany; BioQuant Center, University of Heidelberg, Heidelberg, Germany.

Veit R Buchholz (VR)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany; German Center for Infection Research (DZIF), Partner Site Munich, Munich, Germany. Electronic address: veit.buchholz@tum.de.

Simon Grassmann (S)

Institute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich, Germany; Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: simon.grassmann@tum.de.

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