Evidence map›Paper›PMID 38327763›Full record

Observational studyFrontiers in immunology2023

Persistent CD8

Stephanie M LaVergne, Taru S Dutt, Kim McFann, Bridget A Baxter, Tracy L Webb, Kailey Berry, Maddy Tipton, Sophia Stromberg, Brian M Sullivan, Julie Dunn and 2 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Observational
  6. Observational
  7. Review
  8. Inflammatory pathways in patients with post-acute sequelae of COVID-19: The role of the clinical immunologist.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2024
    Review
  9. 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 3 institutions in 1 country.

Stephanie M LaVergne *Department of Environmental Radiological and Health Sciences, Colorado State University, Fort Collins, CO, United States.
Taru S Dutt *Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, United States.
Kim McFannUniversity of Colorado Health, Medical Center of the Rockies, Loveland, CO, United States.
Bridget A BaxterDepartment of Environmental Radiological and Health Sciences, Colorado State University, Fort Collins, CO, United States.
Tracy L WebbDepartment of Clinical Sciences, Colorado State University, Fort Collins, CO, United States.
Kailey BerryDepartment of Molecular, Cellular, and Integrative Neurosciences, Colorado State University, Fort Collins, CO, United States.
Maddy TiptonDepartment of Environmental Radiological and Health Sciences, Colorado State University, Fort Collins, CO, United States.
Sophia StrombergDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO, United States.
Brian M SullivanDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, United States.
Julie DunnUniversity of Colorado Health, Medical Center of the Rockies, Loveland, CO, United States.
Marcela Henao-TamayoDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, United States.
Elizabeth P RyanDepartment of Environmental Radiological and Health Sciences, Colorado State University, Fort Collins, CO, United States.
Colorado State University · USUniversity of Colorado Health · USScripps (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Post-acute sequelae of COVID-19 affects the quality of life of many COVID-19 survivors, yet the etiology of post-acute sequelae of COVID-19 remains unknown. We aimed to determine if persistent inflammation and ongoing T-cell activation during convalescence were a contributing factor to the pathogenesis of post-acute sequelae of COVID-19. Methods: We evaluated 67 individuals diagnosed with COVID-19 by nasopharyngeal polymerase chain reaction for persistent symptoms during convalescence at separate time points occurring up to 180 days post-diagnosis. Fifty-two of these individuals were evaluated longitudinally. We obtained whole blood samples at each study visit, isolated peripheral blood mononuclear cells, and stained for multiple T cell activation markers for flow cytometry analysis. The activation states of participants' CD4 Results: Overall, we found that participants with persistent symptoms had significantly higher levels of inflammation at multiple time points during convalescence when compared to those who fully recovered from COVID-19. Participants with persistent dyspnea, forgetfulness, confusion, and chest pain had significantly higher levels of proliferating effector T-cells (CD8 Discussion: These findings suggest continued CD8+ T-cell activation following SARS-CoV-2 infection in adults experiencing post-acute sequelae of COVID-19 and that the increase in T regulatory cells for a subset of these patients represents the ongoing attempt by the host to reduce inflammation.

Indexed as

COVID-19AdultCD3 ComplexCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell ProliferationChest PainCohort StudiesConvalescenceDisease ProgressionDyspneaHumansInflammationKi-67 AntigenLeukocytes, MononuclearPost-Acute COVID-19 SyndromeCD3 ComplexKi-67 AntigenCD8+ T cellCOVID-19cytotoxic T cellspost-acute sequelae of COVID-19post-COVIDSARS-CoV-2

Identifiers

PMID38327763
PMCPMC10848319
OpenAlexW4391144346

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.