Evidence map›Paper›PMID 32841340›Full record

ArticleBlood advances2020

Human NK cells prime inflammatory DC precursors to induce Tc17 differentiation.

Maria A Clavijo-Salomon, Rosalba Salcedo, Soumen Roy, Rodrigo X das Neves, Amiran Dzutsev, Helioswilton Sales-Campos, Karen Steponavicius-Cruz Borbely, Lucia Silla, Jordan S Orange, Emily M Mace and 2 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. NK Cells in Cancer: Mechanisms of Dysfunction and Therapeutic Potential.International journal of molecular sciences · 2023
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 4 countries.

Maria A Clavijo-SalomonLaboratory of Integrative Cancer Immunology, Center for Cancer Research, and.
Rosalba SalcedoLaboratory of Integrative Cancer Immunology, Center for Cancer Research, and.
Soumen RoyLaboratory of Integrative Cancer Immunology, Center for Cancer Research, and.
Rodrigo X das NevesLaboratory of Integrative Cancer Immunology, Center for Cancer Research, and.
Amiran DzutsevLaboratory of Integrative Cancer Immunology, Center for Cancer Research, and.
Helioswilton Sales-CamposLaboratory of Integrative Cancer Immunology, Center for Cancer Research, and.
Karen Steponavicius-Cruz BorbelyLaboratory of Tumor Immunology, Department of Immunology, Institute of Biomedical Sciences, and.
Lucia SillaCellular Technology and Therapy Center, Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil.
Jordan S OrangeDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY; and.
Emily M MaceDepartment of Pediatrics, Columbia University Irving Medical Center, New York, NY; and.
José A M BarbutoLaboratory of Tumor Immunology, Department of Immunology, Institute of Biomedical Sciences, and.
Giorgio TrinchieriLaboratory of Integrative Cancer Immunology, Center for Cancer Research, and.
National Institutes of Health · USColumbia University Irving Medical Center · USHospital de Clínicas de Porto Alegre · BRInstitute of Biomedical Science · GBUniversidade de São Paulo · BR

Funding

Regulation of human dendritic cell activationZIABC011152 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TRINCHIERI, GIORGIO · 2009 to 2025
$8.6M
GENETIC, IMMUNOLOGIC AND MECHANISTIC BASIS OF HUMAN NK CELL DEFICIENCYR01AI120989 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ORANGE, JORDAN SCOTT · 2016 to 2025
$7.7M
DETERMINING THE ROLE OF THE REPLICATIVE HELICASE IN HUMAN NK CELL DEVELOPMENTR01AI137275 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MACE, EMILY MARGARET · 2018 to 2022
$1.9M
Intramural NIH HHS ZIA BC011152NIAID NIH HHS R01 AI120989NIAID NIH HHS R01 AI137275
6 · The paper itself

Abstract

Adaptive immune responses are acknowledged to evolve from innate immunity. However, limited information exists regarding whether encounters between innate cells direct the generation of specialized T-cell subsets. We aim to understand how natural killer (NK) cells modulate cell-mediated immunity in humans. We found that human CD14+CD16- monocytes that differentiate into inflammatory dendritic cells (DCs) are shaped at the early stages of differentiation by cell-to-cell interactions with NK cells. Although a fraction of monocytes is eliminated by NK-cell-mediated cytotoxicity, the polarization of interferon-γ (IFN-γ) at the NKp30-stabilized synapses triggers a stable IFN-γ signature in surviving monocytes that persists after their differentiation into DCs. Notably, NK-cell-instructed DCs drive the priming of type 17 CD8+ T cells (Tc17) with the capacity to produce IFN-γ and interleukin-17A. Compared with healthy donors, this cellular network is impaired in patients with classical NK-cell deficiency driven by mutations in the GATA2 gene. Our findings reveal a previously unrecognized connection by which Tc17-mediated immunity might be regulated by NK-cell-mediated tuning of antigen-presenting cells.

Indexed as

Dendritic CellsKiller Cells, NaturalCell DifferentiationCells, CulturedHumansInterferon-gammaInterferon-gamma

Identifiers

PMID32841340
PMCPMC7448590
OpenAlexW3080606762

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.