Evidence map›Paper›PMID 33811059›Full record

ArticleScience immunology2021

Human plasmacytoid dendritic cells mount a distinct antiviral response to virus-infected cells.

Tae Jin Yun, Suzu Igarashi, Haoquan Zhao, Oriana A Perez, Marcus R Pereira, Emmanuel Zorn, Yufeng Shen, Felicia Goodrum, Adeeb Rahman, Peter A Sims and 2 more

Open access · greenAbstract read
In one paragraph

Article in Science immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Immune cell disorder in viral pneumonia.Journal of translational medicine · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Dendritic cell maturation in cancer.Nature reviews. Cancer · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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 4 institutions in 1 country.

Tae Jin YunDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.ORCID 0000-0003-2728-7227
Suzu IgarashiDepartment of Immunobiology, BIO5 Institute, University of Arizona, Tucson, AZ 85721, USA.
Haoquan ZhaoDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Oriana A PerezDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.ORCID 0000-0002-4093-1147
Marcus R PereiraDepartment of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.ORCID 0000-0002-9214-9122
Emmanuel ZornColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY 10032, USA.ORCID 0000-0001-9985-8389
Yufeng ShenDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Felicia GoodrumDepartment of Immunobiology, BIO5 Institute, University of Arizona, Tucson, AZ 85721, USA.ORCID 0000-0002-6646-7290
Adeeb RahmanPrecision Immunology Institute, Department of Genetics and Genomic Sciences, Tisch Cancer Institute, and Human Immune Monitoring Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID 0000-0002-8620-3161
Peter A SimsDepartment of Systems Biology, Department of Biochemistry & Molecular Biophysics, and Sulzberger Columbia Genome Center, Columbia University Irving Medical Center, New York, NY 10032, USA.ORCID 0000-0002-3921-4837
Donna L FarberColumbia Center for Translational Immunology, Columbia University Irving Medical Center, New York, NY 10032, USA.ORCID 0000-0001-8236-9183
Boris ReizisDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA. boris.reizis@nyulangone.org.ORCID 0000-0003-1140-7853
Columbia University Irving Medical Center · USNew York University · USUniversity of Arizona · USTisch Hospital · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Richard Lewis Possemato · 1985 to 2026
$83.1M
Viral Assays CoreU19AI128949 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Donna L. Farber, Peter Alan Sims · 2017 to 2026
$26.4M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR37AI072571 · NIAID · UNIVERSITY OF CHICAGO · PI Boris Reizis · 2018 to 2026
$5.3M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR01AI072571 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2008 to 2017
$4.1M
Scanning Electron Microscope with 3ViewS10OD019974 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LIANG, FENGXIA · 2016 to 2016
$1.1M
Helios Mass CytometerS10OD023547 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI RAHMAN, ADEEB HABIBUR · 2017 to 2017
$667k
Dynamic Spatiotemporal Analysis of Immune Cells in the Tumor MicroenvironmentF32CA232666 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PEREZ, ORIANA · 2018 to 2020
$150k
NCI NIH HHS F32 CA232666NCI NIH HHS P30 CA016087NIAID NIH HHS R01 AI072571NIAID NIH HHS R37 AI072571NIAID NIH HHS U19 AI128949NIH HHS S10 OD019974NIH HHS S10 OD023547
6 · The paper itself

Abstract

Plasmacytoid dendritic cells (pDCs) can rapidly produce interferons and other soluble factors in response to extracellular viruses or virus mimics such as CpG-containing DNA. pDCs can also recognize live cells infected with certain RNA viruses, but the relevance and functional consequences of such recognition remain unclear. We studied the response of primary DCs to the prototypical persistent DNA virus, human cytomegalovirus (CMV). Human pDCs produced high amounts of type I interferon (IFN-I) when incubated with live CMV-infected fibroblasts but not with free CMV; the response involved integrin-mediated adhesion, transfer of DNA-containing virions to pDCs, and the recognition of DNA through TLR9. Compared with transient polyfunctional responses to CpG or free influenza virus, pDC response to CMV-infected cells was long-lasting, dominated by the production of IFN-I and IFN-III, and lacked diversification into functionally distinct populations. Similarly, pDC activation by influenza-infected lung epithelial cells was highly efficient, prolonged, and dominated by interferon production. Prolonged pDC activation by CMV-infected cells facilitated the activation of natural killer cells critical for CMV control. Last, patients with CMV viremia harbored phenotypically activated pDCs and increased circulating IFN-I and IFN-III. Thus, recognition of live infected cells is a mechanism of virus detection by pDCs that elicits a unique antiviral immune response.

Indexed as

Cells, CulturedCoculture TechniquesCpG IslandsCytomegalovirusDendritic CellsFibroblastsHost Microbial InteractionsHumansInterferon LambdaInterferonsInterferon Type IPrimary Cell CultureInterferon LambdaInterferonsInterferon Type I

Identifiers

PMID33811059
PMCPMC8221820
OpenAlexW3149653622

What OpenQuestion holds

Textmetadata
LicenceTDM
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.