The Variable Genomic NK Cell Receptor Locus Is a Key Determinant of CD4+ T Cell Responses During Viral Infection.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2020
Historique:
received: 08 07 2019
accepted: 27 01 2020
entrez: 11 3 2020
pubmed: 11 3 2020
medline: 20 2 2021
Statut: epublish

Résumé

Increasing evidence points to a key role for NK cells in controlling adaptive immune responses. In studies examining the role of CD1d on CD4+ T cell responses, we found that a line of CD1d-deficient mice on the C57BL/6J background had a homozygous 129 locus on chromosome 6 containing the entire NK cell gene cluster. Mice possessing this locus (C57BL/6.NKC

Identifiants

pubmed: 32153566
doi: 10.3389/fimmu.2020.00197
pmc: PMC7044186
doi:

Substances chimiques

Antigens, CD1d 0
CD1d antigen, mouse 0
Interferon Type I 0
Pore Forming Cytotoxic Proteins 0
Receptors, Natural Killer Cell 0
perforin, mouse 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

197

Subventions

Organisme : NIAMS NIH HHS
ID : P30 AR070549
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI057753
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI074743
Pays : United States
Organisme : NIAID NIH HHS
ID : R56 AI057753
Pays : United States

Informations de copyright

Copyright © 2020 Raynor, Lin, Hummel, Lampe, Jordan, Hoebe and Hildeman.

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Auteurs

Jana Raynor (J)

Division of Immunobiology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Immunology Graduate Program, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Adora Lin (A)

Division of Immunobiology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Immunology Graduate Program, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Sarah A Hummel (SA)

Division of Immunobiology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Kristin Lampe (K)

Division of Immunobiology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Michael Jordan (M)

Division of Immunobiology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Kasper Hoebe (K)

Division of Immunobiology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

David A Hildeman (DA)

Division of Immunobiology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

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Classifications MeSH