Evidence map›Paper›PMID 34867943›Full record

ArticleFrontiers in immunology2021

Data-Driven Analysis of COVID-19 Reveals Persistent Immune Abnormalities in Convalescent Severe Individuals.

Jackwee Lim, Kia Joo Puan, Liang Wei Wang, Karen Wei Weng Teng, Chiew Yee Loh, Kim Peng Tan, Guillaume Carissimo, Yi-Hao Chan, Chek Meng Poh, Cheryl Yi-Pin Lee and 23 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

33 authors at 8 institutions in 2 countries.

Jackwee LimSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Kia Joo PuanSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Liang Wei WangSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Karen Wei Weng TengSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Chiew Yee LohSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Kim Peng TanSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Guillaume CarissimoSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Yi-Hao ChanSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Chek Meng PohSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Cheryl Yi-Pin LeeSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Siew-Wai FongSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Nicholas Kim-Wah YeoSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Rhonda Sin-Ling CheeSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Siti Naqiah AmrunSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Zi Wei ChangSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Matthew Zirui TaySingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Anthony Torres-RuestaSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Norman Leo FernandezSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Wilson HowSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Anand Kumar AndiappanSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Wendy LeeSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Kaibo DuanSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Seow-Yen TanDepartment of Infectious Diseases, Changi General Hospital, Singapore, Singapore.
Gabriel YanDepartment of Medicine, National University Hospital, Singapore, Singapore.
Shirin KalimuddinDepartment of Infectious Diseases, Singapore General Hospital, Singapore, Singapore.
David Chien LyeNational Centre for Infectious Diseases, Singapore, Singapore.
Yee-Sin LeoNational Centre for Infectious Diseases, Singapore, Singapore.
Sean W X OngNational Centre for Infectious Diseases, Singapore, Singapore.
Barnaby E YoungNational Centre for Infectious Diseases, Singapore, Singapore.
Laurent ReniaSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Lisa F P NgSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Bernett LeeSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Olaf RötzschkeSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Singapore Immunology Network · SGAgency for Science, Technology and Research · SGNational Centre for Infectious Diseases · SGNational University of Singapore · SGChangi General Hospital · SGDuke-NUS Medical School · SGNational University Hospital · SGTan Tock Seng Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe SARS-CoV-2 infection can trigger uncontrolled innate and adaptive immune responses, which are commonly associated with lymphopenia and increased neutrophil counts. However, whether the immune abnormalities observed in mild to severely infected patients persist into convalescence remains unclear. Herein, comparisons were drawn between the immune responses of COVID-19 infected and convalescent adults. Strikingly, survivors of severe COVID-19 had decreased proportions of NKT and Vδ2 T cells, and increased proportions of low-density neutrophils, IgA+/CD86+/CD123+ non-classical monocytes and hyperactivated HLADR+CD38+ CD8+ T cells, and elevated levels of pro-inflammatory cytokines such as hepatocyte growth factor and vascular endothelial growth factor A, long after virus clearance. Our study suggests potential immune correlates of "long COVID-19", and defines key cells and cytokines that delineate true and quasi-convalescent states.

Indexed as

AdultAgedCohort StudiesConvalescenceCOVID-19FemaleHumansMaleMiddle AgedPost-Acute COVID-19 SyndromeSARS-CoV-2active infectionCOVID-19cytokine profileimmune recoveryimmunophenotypinginflammationSARS – CoV – 2severity

Identifiers

PMID34867943
PMCPMC8640498
OpenAlexW3216279516

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.