Evidence map›Paper›PMID 38178158›Full record

ArticleVirology journal2024

Chronic COVID-19 infection in an immunosuppressed patient shows changes in lineage over time: a case report.

Sheridan J C Baker, Landry E Nfonsam, Daniela Leto, Candy Rutherford, Marek Smieja, Andrew G McArthur

Open access · goldAbstract readCase Reports
In one paragraph

Article in Virology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Prevalence and symptoms of Long Covid-19 in the workplace.Occupational medicine (Oxford, England) · 2025
    Pooled it
  2. Review
  3. Article
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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

6 authors at 4 institutions in 1 country.

Sheridan J C BakerDavid Braley Centre for Antibiotic Discovery, McMaster University, Hamilton, ON, Canada.
Landry E NfonsamDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Daniela LetoDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Candy RutherfordHamilton Regional Laboratory Medicine Program, St Joseph's Healthcare, Hamilton, ON, Canada.
Marek SmiejaMichael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON, Canada.
Andrew G McArthurDavid Braley Centre for Antibiotic Discovery, McMaster University, Hamilton, ON, Canada. mcarthua@mcmaster.ca.
Hamilton Regional Laboratory Medicine Program · CAMcMaster University · CAMcMaster University Medical Centre · CASt. Joseph’s Healthcare Hamilton · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe COVID-19 pandemic, caused by the Severe Acute Respiratory Syndrome Coronavirus 2 virus, emerged in late 2019 and spready globally. Many effects of infection with this pathogen are still unknown, with both chronic and repeated COVID-19 infection producing novel pathologies. CASE PRESENTATION: An immunocompromised patient presented with chronic COVID-19 infection. The patient had history of Hodgkin's lymphoma, treated with chemotherapy and stem cell transplant. During the course of their treatment, eleven respiratory samples from the patient were analyzed by whole-genome sequencing followed by lineage identification. Whole-genome sequencing of the virus present in the patient over time revealed that the patient at various timepoints harboured three different lineages of the virus. The patient was initially infected with the B.1.1.176 lineage before coinfection with BA.1. When the patient was coinfected with both B.1.1.176 and BA.1, the viral populations were found in approximately equal proportions within the patient based on sequencing read abundance. Upon further sampling, the lineage present within the patient during the final two timepoints was found to be BA.2.9. The patient eventually developed respiratory failure and died.

conclusionsThis case study shows an example of the changes that can happen within an immunocompromised patient who is infected with COVID-19 multiple times. Furthermore, this case demonstrates how simultaneous coinfection with two lineages of COVID-19 can lead to unclear lineage assignment by standard methods, which are resolved by further investigation. When analyzing chronic COVID-19 infection and reinfection cases, care must be taken to properly identify the lineages of the virus present.

Indexed as

CoinfectionCOVID-19HumansImmunocompromised HostPandemicsSARS-CoV-2CancerChronic COVID-19COVID-19COVID-19 reinfectionHodgkin’s lymphomaImmunocompromised

Identifiers

PMID38178158
PMCPMC10768205
OpenAlexW4390590317

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.