Cutting Edge: Inhibition of the Interaction of NK Inhibitory Receptors with MHC Class I Augments Antiviral and Antitumor Immunity.


Journal

Journal of immunology (Baltimore, Md. : 1950)
ISSN: 1550-6606
Titre abrégé: J Immunol
Pays: United States
ID NLM: 2985117R

Informations de publication

Date de publication:
01 08 2020
Historique:
received: 21 04 2020
accepted: 22 05 2020
pubmed: 1 7 2020
medline: 16 3 2021
entrez: 1 7 2020
Statut: ppublish

Résumé

NK cells recognize MHC class I (MHC-I) Ags via stochastically expressed MHC-I-specific inhibitory receptors that prevent NK cell activation via cytoplasmic ITIM. We have identified a pan anti-MHC-I mAb that blocks NK cell inhibitory receptor binding at a site distinct from the TCR binding site. Treatment of unmanipulated mice with this mAb disrupted immune homeostasis, markedly activated NK and memory phenotype T cells, enhanced immune responses against transplanted tumors, and augmented responses to acute and chronic viral infection. mAbs of this type represent novel checkpoint inhibitors in tumor immunity, potent tools for the eradication of chronic infection, and may function as adjuvants for the augmentation of the immune response to weak vaccines.

Identifiants

pubmed: 32601097
pii: jimmunol.2000412
doi: 10.4049/jimmunol.2000412
pmc: PMC7369225
mid: NIHMS1599417
doi:

Substances chimiques

Histocompatibility Antigens Class I 0
Receptors, Natural Killer Cell 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

567-572

Subventions

Organisme : Intramural NIH HHS
ID : Z01 AI000224
Pays : United States

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Auteurs

Abir K Panda (AK)

Cellular Immunology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.

Arunakumar Gangaplara (A)

Laboratory of Early Sickle Mortality Prevention, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892; and.

Maja Buszko (M)

Cellular Immunology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.

Kannan Natarajan (K)

Molecular Biology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.

Lisa F Boyd (LF)

Molecular Biology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.

Suveena Sharma (S)

Cellular Immunology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.

David H Margulies (DH)

Molecular Biology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.

Ethan M Shevach (EM)

Cellular Immunology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892; eshevach@niaid.nih.gov.

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Classifications MeSH