Evidence map›Paper›PMID 32655581›Full record

ReviewFrontiers in immunology

Flattening the COVID-19 Curve With Natural Killer Cell Based Immunotherapies.

Marisa Market, Leonard Angka, Andre B Martel, Donald Bastin, Oladunni Olanubi, Gayashan Tennakoon, Dominique M Boucher, Juliana Ng, Michele Ardolino, Rebecca C Auer

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed, 1 pooled it
11.3field-weighted citation impact, top 1% 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

104 citing papers in PubMed, 1 synthesis or guideline pooled it, 155 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. A comprehensive overview of monkeypox virus disease.Tropical medicine and health · 2026
    Review
  5. Review
  6. Immune cell disorder in viral pneumonia.Journal of translational medicine · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Off-the-shelf allogeneic natural killer cells for the treatment of COVID-19.Molecular therapy. Methods & clinical development · 2024
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review

44 more citing papers are in PubMed but not listed here.

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

10 authors at 4 institutions in 1 country.

Marisa MarketCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Leonard AngkaCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Andre B MartelCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Donald BastinSchulich School of Medicine, University of Western Ontario, London, ON, Canada.
Oladunni OlanubiCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Gayashan TennakoonCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Dominique M BoucherDepartment of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, ON, Canada.
Juliana NgCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Michele ArdolinoCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Rebecca C AuerCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Ottawa Hospital · CAOttawa Hospital Research InstituteUniversity of Ottawa · CAWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural Killer (NK) cells are innate immune responders critical for viral clearance and immunomodulation. Despite their vital role in viral infection, the contribution of NK cells in fighting SARS-CoV-2 has not yet been directly investigated. Insights into pathophysiology and therapeutic opportunities can therefore be inferred from studies assessing NK cell phenotype and function during SARS, MERS, and COVID-19. These studies suggest a reduction in circulating NK cell numbers and/or an exhausted phenotype following infection and hint toward the dampening of NK cell responses by coronaviruses. Reduced circulating NK cell levels and exhaustion may be directly responsible for the progression and severity of COVID-19. Conversely, in light of data linking inflammation with coronavirus disease severity, it is necessary to examine NK cell potential in mediating immunopathology. A common feature of coronavirus infections is that significant morbidity and mortality is associated with lung injury and acute respiratory distress syndrome resulting from an exaggerated immune response, of which NK cells are an important component. In this review, we summarize the current understanding of how NK cells respond in both early and late coronavirus infections, and the implication for ongoing COVID-19 clinical trials. Using this immunological lens, we outline recommendations for therapeutic strategies against COVID-19 in clearing the virus while preventing the harm of immunopathological responses.

Indexed as

Adoptive TransferAdrenal Cortex HormonesAnimalsAnti-Inflammatory Agents, Non-SteroidalAscorbic AcidBetacoronavirusCoronavirus InfectionsCOVID-19CytokinesDisease SusceptibilityHumansImmunity, InnateImmunologic MemoryInterferon Type IKiller Cells, NaturalMiceAdrenal Cortex HormonesAnti-Inflammatory Agents, Non-SteroidalAscorbic AcidCytokinesInterferon Type ICOVID-19immunotherapyinnate immunityinterferonNK cells

Identifiers

PMID32655581
PMCPMC7324763
OpenAlexW3038028872

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.