Evidence map›Paper›PMID 37189479›Full record

ArticleDiagnostics (Basel, Switzerland)2023

Circulating Regulatory T Cell Subsets in Patients with Sarcoidosis.

Igor Kudryavtsev, Yulia Zinchenko, Anna Starshinova, Maria Serebriakova, Anna Malkova, Tatiana Akisheva, Dmitriy Kudlay, Anzhela Glushkova, Piotr Yablonskiy, Yehuda Shoenfeld

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 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
–field-weighted citation impact
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.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Infectious Complications of Pulmonary Sarcoidosis.Journal of clinical medicine · 2024
    Review
  8. Article
  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

10 authors.

Igor KudryavtsevDepartment of Immunology, Institution of Experimental Medicine, 197376 St. Petersburg, Russia.
Yulia ZinchenkoPhthisiopulmonology Department, St. Petersburg Research Institute of Phthisiopulmonology, 194064 St. Petersburg, Russia.ORCID 0000-0001-7856-3530
Anna StarshinovaAlmazov National Medical Research Centre, 197341 St. Petersburg, Russia.
Maria SerebriakovaDepartment of Immunology, Institution of Experimental Medicine, 197376 St. Petersburg, Russia.
Anna MalkovaLaboratory of the Mosaic of Autoimmunity, St. Petersburg State University, 199034 St. Petersburg, Russia.ORCID 0000-0002-6008-1354
Tatiana AkishevaDepartment of Immunology, Institution of Experimental Medicine, 197376 St. Petersburg, Russia.
Dmitriy KudlayDepartment of Pharmacology, Sechenov First Moscow State Medical University, 119992 Moscow, Russia.ORCID 0000-0003-1878-4467
Anzhela GlushkovaBekhterev National Research Medical Center for Psychiatry and Neurology, 19201 St. Petersburg, Russia.
Piotr YablonskiyPhthisiopulmonology Department, St. Petersburg Research Institute of Phthisiopulmonology, 194064 St. Petersburg, Russia.
Yehuda ShoenfeldLaboratory of the Mosaic of Autoimmunity, St. Petersburg State University, 199034 St. Petersburg, Russia.

Funding

The Institute of Legislation and Comparative Law under the Government of the Russian Federation 14.W03.31.0009
6 · The paper itself

Abstract

Over recent years, many researchers have supported the autoimmune theory of sarcoidosis. The presence of uncontrolled inflammatory response on local and system levels in patients with sarcoidosis did not define that the immunoregulatory mechanisms could be affected. The aim of this study was to evaluate the distribution and the disturbance circulating Treg cell subsets in the peripheral blood in patients with sarcoidosis. MATERIALS AND

methodsA prospective comparative study was performed in 2016-2018 (34 patients with sarcoidosis (men (67.6%), women (32.3%)) were examined). Healthy subjects-the control group ( RESULTS OF THE STUDY: Primarily, we found that patients with sarcoidosis had decreased absolute numbers of Treg cells in circulation. We noted that the level of CCR7-expressing Tregs decreased in patients with sarcoidosis vs. the control group (65.55% (60.08; 70.60) vs. 76.93% (69.59; 79.86) with

conclusionsOur data indicated a decrease in circulating Tregs absolute numbers and several alterations in Treg cell subsets. Moreover, our results highlight the presence of increased levels of CM CXCR5+ follicular Tregs in the periphery that could be linked with the imbalance of follicular Th cell subsets and alterations in B cell, based on the immune response. The balance between the two functionally distinct Treg cell populations-Th1-like and Th17-like Tregs-could be used in sarcoidosis diagnosis and the determination of prognosis and disease outcomes. Furthermore, we want to declare that analysis of Treg numbers of phenotypes could fully characterize their functional activity in peripherally inflamed tissues.

Indexed as

autoimmunityfollicular TregpathogenesissarcoidosisTregTreg subsets

Identifiers

PMID37189479
PMCPMC10137313

What Socratic holds

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LicenceCC BY
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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 Socratic graph.