Evidence map›Paper›PMID 36326397›Full record

ArticleTurkish journal of medical sciences2022

The role of CD8+ regulatory T cells and B cell subsets in patients with COVID-19.

Hülya Uçaryılmaz, Dilek Ergün, Hüsamettin Vatansev, Hande Köksal, Onur Ural, Uğur Arslan, Hasibe Artaç

Open access · bronzeAbstract read
In one paragraph

Article in Turkish journal of medical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

7 authors at 1 institution in 1 country.

Hülya UçaryılmazDepartment of Medical Biology, Faculty of Medicine, Selçuk University, Konya, Turkey.
Dilek ErgünDepartment of Chest Disease, Faculty of Medicine, Selçuk University, Konya, Turkey.
Hüsamettin VatansevDepartment of Medical Biochemistry, Faculty of Medicine, Selçuk University, Konya, Turkey.
Hande KöksalDepartment of General Surgery, Hamidiye Faculty of Medicine, University of Health Sciences, Konya, Turkey.
Onur UralDepartment of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Selçuk University, Konya, Turkey.
Uğur ArslanDepartment of Medical Microbiology, Faculty of Medicine, Selçuk University, Konya, Turkey.
Hasibe ArtaçDepartment of Pediatric Immunology and Allergy, Faculty of Medicine, Selçuk University, Konya, Turkey.
Selçuk University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronavirus disease 2019 (COVID-19) has a wide clinical spectrum from asymptomatic to mild, moderate, and severe cases. There are still many unknowns about the role of immunoregulatory mechanisms in COVID-19. We aimed to study regulatory T cells (Tregs) and B cell subsets and evaluate their correlations with severity of COVID-19.

methodsIn total, 50 patients with COVID-19 confirmed by PCR (mean age = 49.9 ± 12.8 years) and 40 healthy control (mean age = 47.9 ± 14.7 years) were included in this study. The patients were classified as 14 mild (median age = 35.5 [24-73] years), 22 moderate (median age = 51.5 [28-67] years) and 14 severe (median age = 55.5 [42-67] years). Within 24 h of admission, flow cytometry was used to assess the lymphocyte subsets, Tregs and Bregs without receiving any relevant medication.

resultsIn all patients with COVID-19, the proportion of CD3+CD8+ T cells was reduced (p = 0.004) and the CD8+ Tregs were increased compared with control (p = 0.001). While the levels of regulatory B cells, plasmablasts, and mature naive B cells were found to be significantly high, primarily memory B-cell levels were low in all patients compared with controls (p < 0.05). Total CD3+ T cells were negatively correlated with the length of stay in the hospital (r = -0.286, p = 0.044). DISCUSSION: The changes in T and B cell subsets may show the dysregulation in the immunity of patients with COVID-19. In this context, the association between CD8+ Tregs and COVID-19 severity may help clinicians to predict severe and fatal COVID-19 in hospitalized patients.

Indexed as

B-Lymphocyte SubsetsCOVID-19AdultCD8-Positive T-LymphocytesHumansLymphocyte CountMiddle AgedT-Lymphocytes, RegulatoryCOVID-19regulatory B cellsregulatory T cellsSARS-CoV-2

Identifiers

PMID36326397
PMCPMC10388126
OpenAlexW4291498113

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Registered trials

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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.