Evidence map›Paper›PMID 34025675›Full record

ArticleFrontiers in immunology2021

Longitudinal Analysis of COVID-19 Patients Shows Age-Associated T Cell Changes Independent of Ongoing Ill-Health.

Liam Townsend, Adam H Dyer, Aifric Naughton, Rachel Kiersey, Dean Holden, Mary Gardiner, Joanne Dowds, Kate O'Brien, Ciaran Bannan, Parthiban Nadarajan and 8 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 3 pooled it
5.3field-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

35 citing papers in PubMed, 3 syntheses or guidelines pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Blood Biomarkers of Long COVID: A Systematic Review.Molecular diagnosis & therapy · 2024
    Pooled it
  3. Pooled it
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  15. The role of immune activation and antigen persistence in acute and long COVID.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2023
    Review
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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

18 authors at 2 institutions in 1 country.

Liam TownsendDepartment of Infectious Diseases, St James's Hospital, Dublin, Ireland.
Adam H DyerDepartment of Medical Gerontology, School of Medicine, Trinity Translational Medicine Institute, Trinity College Dublin, Dublin, Ireland.
Aifric NaughtonDepartment of Immunology, St James's Hospital, Dublin, Ireland.
Rachel KierseyDepartment of Immunology, St James's Hospital, Dublin, Ireland.
Dean HoldenDepartment of Immunology, St James's Hospital, Dublin, Ireland.
Mary GardinerDepartment of Immunology, St James's Hospital, Dublin, Ireland.
Joanne DowdsDepartment of Physiotherapy, St James's Hospital, Dublin, Ireland.
Kate O'BrienDepartment of Physiotherapy, St James's Hospital, Dublin, Ireland.
Ciaran BannanDepartment of Infectious Diseases, St James's Hospital, Dublin, Ireland.
Parthiban NadarajanDepartment of Respiratory Medicine, St James's Hospital, Dublin, Ireland.
Jean DunneDepartment of Immunology, St James's Hospital, Dublin, Ireland.
Ignacio Martin-LoechesDepartment of Intensive Care Medicine, St James's Hospital, Dublin, Ireland.
Padraic G FallonSchool of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
Colm BerginDepartment of Infectious Diseases, St James's Hospital, Dublin, Ireland.
Cliona O'FarrellySchool of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
Cliona Ni CheallaighDepartment of Infectious Diseases, St James's Hospital, Dublin, Ireland.
Nollaig M BourkeDepartment of Medical Gerontology, School of Medicine, Trinity Translational Medicine Institute, Trinity College Dublin, Dublin, Ireland.
Niall ConlonDepartment of Immunology, St James's Hospital, Dublin, Ireland.
St. James's Hospital · IETrinity College Dublin · IE

Funding

Wellcome Trust
6 · The paper itself

Abstract

Objectives: The immunological and inflammatory changes following acute COVID-19 are hugely variable. Persistent clinical symptoms following resolution of initial infection, termed Methods: We performed paired immunophenotyping at initial SARS-CoV-2 infection and convalescence (n=40, median 68 days) and validated findings in 71 further patients at median 101 days convalescence. Results were compared to 40 pre-pandemic controls. Fatigue and exercise tolerance were assessed as cardinal features of Results: We identify persistent expansion of intermediate monocytes, effector CD8+, activated CD4+ and CD8+ T cells, and reduced naïve CD4+ and CD8+ T cells at 68 days, with activated CD8+ T cells remaining increased at 101 days. Patients >60 years also demonstrate reduced naïve CD4+ and CD8+ T cells and expanded activated CD4+ T cells at 101 days. Ill-health, fatigue, and reduced exercise tolerance were common in this cohort. These symptoms were not associated with immune cell populations or circulating inflammatory cytokines. Conclusion: We demonstrate myeloid recovery but persistent T cell abnormalities in convalescent COVID-19 patients more than three months after initial infection. These changes are more marked with age and are independent of ongoing subjective ill-health, fatigue and reduced exercise tolerance.

Indexed as

AdultAgedAge FactorsAgingCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCohort StudiesConvalescenceCOVID-19FemaleHumansImmunophenotypingLongitudinal StudiesLymphocyte ActivationMaleMiddle AgedageingCOVID-19fatigueimmune recoveryimmunophenotypingT cells

Identifiers

PMID34025675
PMCPMC8138306
OpenAlexW3163235228

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.