Evidence map›Paper›PMID 32784290›Full record

Trial reportThe Journal of clinical investigation2020

COVID-19 severity associates with pulmonary redistribution of CD1c+ DCs and inflammatory transitional and nonclassical monocytes.

Ildefonso Sánchez-Cerrillo, Pedro Landete, Beatriz Aldave, Santiago Sánchez-Alonso, Ana Sánchez-Azofra, Ana Marcos-Jiménez, Elena Ávalos, Ana Alcaraz-Serna, Ignacio de Los Santos, Tamara Mateu-Albero and 15 more

Abstract readClinical Trial
In one paragraph

Trial report in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

138 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Mucosal immune response in biology, disease prevention and treatment.Signal transduction and targeted therapy · 2025
    Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Monocytes in pneumonia: Functional plasticity and innate memory (Review).International journal of molecular medicine · 2026
    Review
  6. Coordinated expansion of CD163bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Observational
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors.

Ildefonso Sánchez-CerrilloImmunology Unit.
Pedro LandetePneumology Department.
Beatriz AldavePneumology Department.
Santiago Sánchez-AlonsoImmunology Unit.
Ana Sánchez-AzofraPneumology Department.
Ana Marcos-JiménezImmunology Unit.
Elena ÁvalosPneumology Department.
Ana Alcaraz-SernaImmunology Unit.
Ignacio de Los SantosInfectious Diseases Division.
Tamara Mateu-AlberoImmunology Unit.
Laura EsparciaImmunology Unit.
Celia López-SanzImmunology Unit.
Pedro Martínez-FletaImmunology Unit.
Ligia GabrieImmunology Unit.
Luciana Del Campo GuerolaImmunology Unit.
Hortensia de la FuenteImmunology Unit.
María J CalzadaImmunology Unit.
Isidoro González-ÁlvaroRheumatology Service from Hospital Universitario de la Princesa and Instituto de Investigación Sanitaria Princesa, Madrid, Spain.
Arantzazu AlfrancaImmunology Unit.
Francisco Sánchez-MadridImmunology Unit.
Cecilia Muñoz-CallejaImmunology Unit.
Joan B SorianoPneumology Department.
Julio AncocheaPneumology Department.
Enrique Martín-GayoImmunology Unit.
REINMUN-COVID and EDEPIMIC groups

Funding

Tailored induction of HIV-1 specific immunity through engineered dendritic cell vaccinesR21AI140930 · NIAID · UNIVERSIDAD AUTONOMA DE MADRID · PI MARTIN-GAYO, ENRIQUE · 2018 to 2019
$297k
NIAID NIH HHS R21 AI140930
6 · The paper itself

Abstract

SARS-CoV-2 is responsible for the development of coronavirus disease 2019 (COVID-19) in infected individuals, who can either exhibit mild symptoms or progress toward a life-threatening acute respiratory distress syndrome (ARDS). Exacerbated inflammation and dysregulated immune responses involving T and myeloid cells occur in COVID-19 patients with severe clinical progression. However, the differential contribution of specific subsets of dendritic cells and monocytes to ARDS is still poorly understood. In addition, the role of CD8+ T cells present in the lung of COVID-19 patients and relevant for viral control has not been characterized. Here, we have studied the frequencies and activation profiles of dendritic cells and monocytes present in the blood and lung of COVID-19 patients with different clinical severity in comparison with healthy individuals. Furthermore, these subpopulations and their association with antiviral effector CD8+ T cell subsets were also characterized in lung infiltrates from critical COVID-19 patients. Our results indicate that inflammatory transitional and nonclassical monocytes and CD1c+ conventional dendritic cells preferentially migrate from blood to lungs in patients with severe COVID-19. Thus, this study increases the knowledge of specific myeloid subsets involved in the pathogenesis of COVID-19 disease and could be useful for the design of therapeutic strategies for fighting SARS-CoV-2 infection.

Indexed as

AdultAgedAged, 80 and overAntigens, CD1CD8-Positive T-LymphocytesCell MovementCOVID-19Dendritic CellsFemaleGlycoproteinsHumansLungMaleMiddle AgedMonocytesRespiratory Distress SyndromeAntigens, CD1CD1C protein, humanGlycoproteinsCOVID-19Dendritic cellsImmunologyMonocytesT cells

Identifiers

PMID32784290
PMCPMC7685723

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.